Label: CAMPTOSAR- irinotecan hydrochloride injection, solution 

  • NDC Code(s): 0009-7529-01, 0009-7529-02, 0009-7529-03, 0009-7529-04, view more
    0009-7529-05
  • Packager: Pharmacia and Upjohn Company
  • Category: HUMAN PRESCRIPTION DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: New Drug Application

Drug Label Information

Updated 07/12

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  • BOXED WARNING(What is this?)

    WARNING: DIARRHEA AND MYELOSUPPRESSION

    • Early and late forms of diarrhea can occur. Early diarrhea may be accompanied by cholinergic symptoms which may be prevented or ameliorated by atropine. Late diarrhea can be life threatening and should be treated promptly with loperamide. Monitor patients with diarrhea and give fluid and electrolytes as needed. Institute antibiotic therapy if patients develop ileus, fever, or severe neutropenia. Interrupt CAMPTOSAR and reduce subsequent doses if severe diarrhea occurs.
    • Severe myelosuppression may occur.
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  • HIGHLIGHTS OF PRESCRIBING INFORMATION
    These highlights do not include all the information needed to use CAMPTOSAR safely and effectively. See full prescribing information for CAMPTOSAR.
     
    CAMPTOSAR (Irinotecan) Injection, intravenous infusion
    Initial U.S. Approval: 1996

    WARNING: DIARRHEA and MYELOSUPPRESSION

    See full prescribing information for complete boxed warning.

    • Early and late forms of diarrhea can occur. Early diarrhea may be accompanied by cholinergic symptoms which may be prevented or ameliorated by atropine. Late diarrhea can be life threatening and should be treated promptly with loperamide. Monitor patients with diarrhea and give fluid and electrolytes as needed. Institute antibiotic therapy if patients develop ileus, fever, or severe neutropenia. Interrupt CAMPTOSAR and reduce subsequent doses if severe diarrhea occurs.
    • Severe myelosuppression may occur.

    INDICATIONS AND USAGE

    CAMPTOSAR is a topoisomerase inhibitor indicated for:

    • First-line therapy in combination with 5-fluorouracil and leucovorin for patients with metastatic carcinoma of the colon or rectum. (1)
    • Patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy. (1)

    DOSAGE AND ADMINISTRATION

    • Colorectal cancer combination regimen 1: CAMPTOSAR 125 mg/m2 intravenous infusion over 90 minutes on days 1, 8,15, 22 with LV 20 mg/m2 intravenous bolus infusion on days 1, 8, 15, 22 followed by 5-FU intravenous bolus infusion on days 1, 8, 15, 22 every 6 weeks. (2.1)
    • Colorectal cancer combination regimen 2: CAMPTOSAR 180 mg/m2 intravenous infusion over 90 minutes on days 1, 15, 29 with LV 200 mg/m2 intravenous infusion over 2 hours on days 1, 2, 15, 16, 29, 20 followed by 5-FU 400 mg/m2 intravenous bolus infusion on days 1, 2, 15, 16, 29, 30 and 5-FU 600 mg/m2 intravenous infusion over 22 hours on days 1, 2, 15, 16, 29, 30. (2.1)
    • Colorectal cancer single agent regimen 1: CAMPTOSAR 125 mg/m2 intravenous infusion over 90 minutes on days 1, 8, 15, 22 then 2-week rest. (2.2)
    • Colorectal cancer single agent regimen 2: CAMPTOSAR 350 mg/m2 intravenous infusion over 90 minutes on day 1 every 3 weeks. (2.2)

    DOSAGE FORMS AND STRENGTHS

    CAMPTOSAR Injection is available in three single-dose sizes: (3)

    • 2 mL-fill vial containing 40 mg irinotecan hydrochloride injection
    • 5 mL-fill vial containing 100 mg irinotecan hydrochloride injection
    • 15 mL-fill vial containing 300 mg irinotecan hydrochloride injection

    CONTRAINDICATIONS

    • Hypersensitivity to CAMPTOSAR or its excipients (4)

    WARNINGS AND PRECAUTIONS

    • Diarrhea and cholinergic reactions: Early diarrhea (occurring during or shortly after infusion of CAMPTOSAR) is usually transient and may be accompanied by cholinergic symptoms. Consider prophylactic or therapeutic administration of 0.25 mg to 1 mg of intravenous or subcutaneous atropine (unless clinically contraindicated). Late diarrhea (generally occurring more than 24 hours after administration of CAMPTOSAR) can occur. Monitor and replace fluid and electrolytes. Treat with loperamide. Use antibiotic support for ileus and fever. Interrupt CAMPTOSAR and reduce subsequent doses if severe diarrhea occurs. (5.1)
    • Myelosuppression: Manage promptly with antibiotic support. Interrupt CAMPTOSAR and reduce subsequent doses if necessary. (5.2)
    • Patients with Reduced UGT1A1 Activity: Individuals who are homozygous for the UGT1A1*28 allele are at increased risk for neutropenia following initiation of CAMPTOSAR treatment. (5.3)
    • Hypersensitivity: Hypersensitivity reactions including severe anaphylactic or anaphylactoid reactions have been observed. Discontinue CAMPTOSAR if this occurs. (5.4)
    • Renal Impairment/Renal Failure: Rare cases of renal impairment and acute renal failure have been identified, usually in patients who became volume depleted from severe vomiting and/or diarrhea. (5.5)
    • Pulmonary Toxicity: Interstitial Pulmonary Disease (IPD)-like events, including fatalities, have occurred. Interrupt for new or progressive dysnpnea, cough, and fever pending evaluation. If IPD diagnosed, discontinue and institute appropriate treatment as needed. (5.6)
    • Toxicity of the 5 Day Regimen: CAMPTOSAR should not be used in combination with a regimen of 5-FU/LV administered for 4–5 consecutive days every 4 weeks outside of a clinical study. (5.7)
    • Pregnancy: CAMPTOSAR can cause fetal harm when administered to a pregnant woman. (5.9)
    • Patients with Hepatic Impairment: In clinical trials, CAMPTOSAR has not been administered to patients with serum bilirubin > 2.0 mg/dL, or transaminases > 3 times ULN if no liver metastases, or transaminases > 5 times ULN if liver metastases. With the weekly dosage schedule, patients with total bilirubin levels 1.0–2.0 mg/dL had greater likelihood of grade 3–4 neutropenia. (5.10)

    ADVERSE REACTIONS

    Common adverse reactions (≥30%) observed in combination therapy clinical studies are: nausea, vomiting, abdominal pain, diarrhea, constipation, anorexia, mucositis, neutropenia, leukopenia (including lymphocytopenia), anemia, thrombocytopenia, asthenia, pain, fever, infection, abnormal bilirubin, alopecia. (6.1)

    Common adverse reactions (≥30%) observed in single agent therapy clinical studies are: nausea, vomiting, abdominal pain, diarrhea, constipation, anorexia, neutropenia, leukopenia (including lymphocytopenia), anemia, asthenia, fever, body weight decreasing, alopecia. (6.1)


    To report SUSPECTED ADVERSE REACTIONS, contact Pfizer Inc at 1-800-438-1985 or www.pfizer.com or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

    DRUG INTERACTIONS

    • Strong CYP3A4 Inducers: Do not administer for at least 2 weeks prior to initiation of irinotecan therapy. (7.2)
    • Strong CYP3A4 Inhibitors: Discontinue at least 1 week prior to starting irinotecan therapy and do not use during irinotecan therapy. (7.3)

    USE IN SPECIFIC POPULATIONS

    • Nursing Mothers: Discontinue nursing when receiving therapy with CAMPTOSAR. (8.3)
    • Geriatric Use: Closely monitor patients greater than 65 years of age because of a greater risk of early and late diarrhea in this population. (8.5)
    • Patients with Renal Impairment: Use caution and do not use in patients on dialysis. (8.6)
    • Patients with Hepatic Impairment: Use caution. (2.1, 5.10, 8.7, 12.3)

    See 17 for PATIENT COUNSELING INFORMATION.

    Revised: 8/2012

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  • FULL PRESCRIBING INFORMATION: CONTENTS*

    WARNING: DIARRHEA AND MYELOSUPPRESSION

    1 INDICATIONS AND USAGE

    2 DOSAGE AND ADMINISTRATION

    2.1 Colorectal Cancer Combination Regimens 1 and 2

    2.2 Colorectal Single Agent Regimens 1 and 2

    2.3 Dosage in Patients with Reduced UGT1A1 Activity

    2.4 Premedication

    2.5 Preparation of Infusion Solution

    2.6 Safe Handling

    2.7 Extravasation

    3 DOSAGE FORMS AND STRENGTHS

    4 CONTRAINDICATIONS

    5 WARNINGS AND PRECAUTIONS

    5.1 Diarrhea and Cholinergic Reactions

    5.2 Myelosuppression

    5.3 Patients With Reduced UGT1A1 Activity

    5.4 Hypersensitivity

    5.5 Renal Impairment/Renal Failure

    5.6 Pulmonary Toxicity

    5.7 Toxicity of the 5 Day Regimen

    5.8 Increased Toxicity in Patients with Performance Status 2

    5.9 Pregnancy

    5.10 Patients with Hepatic Impairment

    6 ADVERSE REACTIONS

    6.1 Clinical Studies Experience

    6.2 Postmarketing Experience

    7 DRUG INTERACTIONS

    7.1 5-Fluorouracil (5-FU) and Leucovorin (LV)

    7.2 Strong CYP 3A4 Inducers

    7.3 Strong CYP 3A4 Inhibitors

    7.4 Atazanavir Sulfate

    7.5 Drug-Laboratory Test Interactions

    8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    8.3 Nursing Mothers

    8.4 Pediatric Use

    8.5 Geriatric Use

    8.6 Renal Impairment

    8.7 Hepatic Impairment

    10 OVERDOSAGE

    11 DESCRIPTION

    12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    12.2 Pharmacodynamics

    12.3 Pharmacokinetics

    13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    14 CLINICAL STUDIES

    14.1 Metastatic Colorectal Cancer

    15 REFERENCES

    16 HOW SUPPLIED/STORAGE AND HANDLING

    17 PATIENT COUNSELING INFORMATION

    *
    Sections or subsections omitted from the full prescribing information are not listed.
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  • 1 INDICATIONS AND USAGE

    • CAMPTOSAR Injection is indicated as a component of first-line therapy in combination with 5-fluorouracil (5-FU) and leucovorin (LV) for patients with metastatic carcinoma of the colon or rectum.
    • CAMPTOSAR is indicated for patients with metastatic carcinoma of the colon or rectum whose disease has recurred or progressed following initial fluorouracil-based therapy.
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  • 2 DOSAGE AND ADMINISTRATION

    2.1 Colorectal Cancer Combination Regimens 1 and 2

    Administer CAMPTOSAR as a 90-minute intravenous infusion followed by LV and 5-FU. The currently recommended regimens are shown in Table 1.

    A reduction in the starting dose by one dose level of CAMPTOSAR may be considered for patients with any of the following conditions: prior pelvic/abdominal radiotherapy, performance status of 2, or increased bilirubin levels. Dosing for patients with bilirubin >2 mg/dL cannot be recommended because there is insufficient information to recommend a dose in these patients.

    Table 1. Combination-Agent Dosage Regimens and Dose Modifications*
    *
    Dose reductions beyond Dose Level –2 by decrements of ≈ 20% may be warranted for patients continuing to experience toxicity. Provided intolerable toxicity does not develop, treatment with additional cycles may be continued indefinitely as long as patients continue to experience clinical benefit.
    Infusion follows bolus administration.
    Regimen 1
    6-wk cycle with bolus 5-FU/LV
    (next cycle begins on day 43)
    CAMPTOSAR
    LV
    5-FU
    125 mg/m2 intravenous infusion over 90 minutes, days 1,8,15,22
    20 mg/m2 intravenous injection bolus, days 1,8,15,22
    500 mg/m2 intravenous injection bolus, days 1,8,15,22
    Starting Dose & Modified Dose Levels (mg/m2)
    Starting Dose Dose Level -1 Dose Level -2
    CAMPTOSAR 125 100 75
    LV 20 20 20
    5-FU 500 400 300
    Regimen 2
    6-wk cycle with infusional
    5-FU/LV
    (next cycle begins on day 43)
    CAMPTOSAR
    LV
    5-FU Bolus
    5-FU Infusion
    180 mg/m2 intravenous infusion over 90 minutes, days 1,15,29
    200 mg/m2 intravenous infusion over 2 hours, days 1,2,15,16,29,30
    400 mg/m2 intravenous injection bolus, days 1,2,15,16,29,30
    600 mg/m2 intravenous infusion over 22 hours, days 1,2,15,16,29,30
    Starting Dose & Modified Dose Levels (mg/m2)
    Starting Dose Dose Level -1 Dose Level -2
    CAMPTOSAR 180 150 120
    LV 200 200 200
    5-FU Bolus 400 320 240
    5-FU Infusion 600 480 360

    Dosing for patients with bilirubin >2 mg/dL cannot be recommended because there is insufficient information to recommend a dose in these patients [see Warnings and Precautions (5.10), Use in Specific Populations (8.7) and Clinical Pharmacology (12.3)].

    Dose Modifications

    Based on recommended dose levels described in Table 1, Combination Regimens of CAMPTOSAR and Dose Modifications, subsequent doses should be adjusted as suggested in Table 2, Recommended Dose Modifications for Combination Regimens. All dose modifications should be based on the worst preceding toxicity.

    Table 2. Recommended Dose Modifications for CAMPTOSAR/5-Fluorouracil (5-FU)/Leucovorin (LV) Combination Schedules
    Patients should return to pre-treatment bowel function without requiring antidiarrhea medications for at least 24 hours before the next chemotherapy administration. A new cycle of therapy should not begin until the granulocyte count has recovered to ≥1500/mm3, and the platelet count has recovered to ≥100,000/mm3, and treatment-related diarrhea is fully resolved. Treatment should be delayed 1 to 2 weeks to allow for recovery from treatment-related toxicities. If the patient has not recovered after a 2-week delay, consideration should be given to discontinuing therapy.
    Toxicity
    NCI CTC Grade* (Value)
    During a Cycle of Therapy At the Start of Subsequent Cycles of Therapy
    *
    National Cancer Institute Common Toxicity Criteria (version 1.0)
    Relative to the starting dose used in the previous cycle
    Pretreatment
    §
    Excludes alopecia, anorexia, asthenia
    No toxicity Maintain dose level Maintain dose level
    Neutropenia
    1 (1500 to 1999/mm3)
    2 (1000 to 1499/mm3)
    3 (500 to 999/mm3)
    4 (<500/mm3)

    Maintain dose level
    ↓ 1 dose level
    Omit dose until resolved to ≤ grade 2, then ↓ 1 dose level
    Omit dose until resolved to ≤ grade 2, then ↓ 2 dose levels

    Maintain dose level
    Maintain dose level
    ↓ 1 dose level
    ↓ 2 dose levels
    Neutropenic fever Omit dose until resolved, then ↓ 2 dose levels
    Other hematologic toxicities Dose modifications for leukopenia or thrombocytopenia during a cycle of therapy and at the start of subsequent cycles of therapy are also based on NCI toxicity criteria and are the same as recommended for neutropenia above.
    Diarrhea
    1 (2–3 stools/day > pretx)
    2 (4–6 stools/day > pretx)
    3 (7–9 stools/day > pretx)
    4 (≥10 stools/day > pretx)

    Delay dose until resolved to baseline, then give same dose
    Omit dose until resolved to baseline, then ↓ 1 dose level
    Omit dose until resolved to baseline, then ↓ 1 dose level
    Omit dose until resolved to baseline, then ↓ 2 dose levels

    Maintain dose level
    Maintain dose level
    ↓ 1 dose level
    ↓ 2 dose levels
    Other nonhematologic toxicities§
    1
    2
    3
    4

    Maintain dose level
    Omit dose until resolved to ≤ grade 1, then ↓ 1 dose level
    Omit dose until resolved to ≤ grade 2, then ↓ 1 dose level
    Omit dose until resolved to ≤ grade 2, then ↓ 2 dose levels

    For mucositis/stomatitis decrease only 5-FU, not CAMPTOSAR

    Maintain dose level
    Maintain dose level
    ↓ 1 dose level
    ↓ 2 dose levels

    For mucositis/stomatitis decrease only 5-FU, not CAMPTOSAR.

    2.2 Colorectal Single Agent Regimens 1 and 2

    Administer CAMPTOSAR as a 90-minute intravenous infusion. The currently recommended regimens are shown in Table 3.

    A reduction in the starting dose by one dose level of CAMPTOSAR may be considered for patients with any of the following conditions: prior pelvic/abdominal radiotherapy, performance status of 2, or increased bilirubin levels. Dosing for patients with bilirubin >2 mg/dL cannot be recommended because there is insufficient information to recommend a dose in these patients.

    Table 3. Single-Agent Regimens of CAMPTOSAR and Dose Modifications
    *
    Subsequent doses may be adjusted as high as 150 mg/m 2 or to as low as 50 mg/m 2 in 25 to 50 mg/m 2 decrements depending upon individual patient tolerance.
    Provided intolerable toxicity does not develop, treatment with additional cycles may be continued indefinitely as long as patients continue to experience clinical benefit.
    Subsequent doses may be adjusted as low as 200 mg/m 2 in 50 mg/m 2 decrements depending upon individual patient tolerance.
    Regimen 1 (weekly)* 125 mg/m2 intravenous infusion over 90 minutes, days 1,8,15,22 then 2-week rest
      Starting Dose and Modified Dose Levels (mg/m2)
    Starting Dose Dose Level -1 Dose Level -2
    125 100 75
    Regimen 2 (every 3 weeks) 350 mg/m2 intravenous infusion over 90 minutes, once every 3 weeks
      Starting Dose and Modified Dose Levels (mg/m2)
    Starting Dose Dose Level -1 Dose Level -2
    350 300 250

    Dose Modifications

    Based on recommended dose-levels described in Table 3, Single-Agent Regimens of CAMPTOSAR and Dose Modifications, subsequent doses should be adjusted as suggested in Table 4, Recommended Dose Modifications for Single-Agent Schedules. All dose modifications should be based on the worst preceding toxicity.

    Table 4: Recommended Dose Modifications For Single-Agent Schedules*
    A new cycle of therapy should not begin until the granulocyte count has recovered to ≥1500/mm3, and the platelet count has recovered to ≥100,000/mm3, and treatment-related diarrhea is fully resolved. Treatment should be delayed 1 to 2 weeks to allow for recovery from treatment-related toxicities. If the patient has not recovered after a 2-week delay, consideration should be given to discontinuing CAMPTOSAR.
    Worst Toxicity
    NCI Grade (Value)
    During a Cycle of Therapy At the Start of the Next Cycles of Therapy (After Adequate Recovery), Compared with the Starting Dose in the Previous Cycle*
    Weekly Weekly Once Every 3 Weeks
    *
    All dose modifications should be based on the worst preceding toxicity
    National Cancer Institute Common Toxicity Criteria (version 1.0)
    Pretreatment
    §
    Excludes alopecia, anorexia, asthenia
    No toxicity Maintain dose level ↑ 25 mg/m2 up to a maximum dose of 150 mg/m2 Maintain dose level
    Neutropenia
    1 (1500 to 1999/mm3)
    2 (1000 to 1499/mm3)
    3 (500 to 999/mm3)
    4 (<500/mm3)
    Maintain dose level
    ↓ 25 mg/m2
    Omit dose until resolved to ≤ grade 2, then ↓ 25 mg/m2
    Omit dose until resolved to ≤ grade 2, then ↓ 50 mg/m2
    Maintain dose level
    Maintain dose level
    ↓ 25 mg/m2
    ↓ 50 mg/m2
    Maintain dose level
    Maintain dose level
    ↓ 50 mg/m2
    ↓ 50 mg/m2
    Neutropenic fever Omit dose until resolved, then ↓ 50 mg/m2 when resolved ↓ 50 mg/m2 ↓ 50 mg/m2
    Other hematologic toxicities Dose modifications for leukopenia, thrombocytopenia, and anemia during a cycle of therapy and at the start of subsequent cycles of therapy are also based on NCI toxicity criteria and are the same as recommended for neutropenia above.
    Diarrhea
    1 (2–3 stools/day > pretx)
    2 (4–6 stools/day > pretx)
    3 (7–9 stools/day > pretx)
    4 (≥10 stools/day > pretx)
    Maintain dose level
    ↓ 25 mg/m2
    Omit dose until resolved to ≤ grade 2, then ↓ 25 mg/m2
    Omit dose until resolved to ≤ grade 2 then ↓ 50 mg/m2
    Maintain dose level
    Maintain dose level
    ↓ 25 mg/m2
    ↓ 50 mg/m2
    Maintain dose level
    Maintain dose level
    ↓ 50 mg/m2
    ↓ 50 mg/m2
    Other nonhematologic§ toxicities
    1
    2
    3
    4


    Maintain dose level
    ↓ 25 mg/m2
    Omit dose until resolved to ≤ grade 2, then ↓ 25 mg/m2
    Omit dose until resolved to ≤ grade 2, then ↓ 50 mg/m2


    Maintain dose level
    ↓ 25 mg/m2
    ↓ 25 mg/m2
    ↓ 50 mg/m2


    Maintain dose level
    ↓ 50 mg/m2
    ↓ 50 mg/m2
    ↓ 50 mg/m2

    2.3 Dosage in Patients with Reduced UGT1A1 Activity

    When administered in combination with other agents, or as a single-agent, a reduction in the starting dose by at least one level of CAMPTOSAR should be considered for patients known to be homozygous for the UGT1A1*28 allele [see Dosage and Administration (2.1 and 2.2) and Warnings and Precautions (5.3)]. However, the precise dose reduction in this patient population is not known, and subsequent dose modifications should be considered based on individual patient tolerance to treatment (see Tables 1–4).

    2.4 Premedication

    It is recommended that patients receive premedication with antiemetic agents. In clinical studies of the weekly dosage schedule, the majority of patients received 10 mg of dexamethasone given in conjunction with another type of antiemetic agent, such as a 5-HT3 blocker (e.g., ondansetron or granisetron). Antiemetic agents should be given on the day of treatment, starting at least 30 minutes before administration of CAMPTOSAR. Physicians should also consider providing patients with an antiemetic regimen (e.g., prochlorperazine) for subsequent use as needed. A similar antiemetic regimen should be used with Camptosar in combination therapy.

    Prophylactic or therapeutic administration of atropine should be considered in patients experiencing cholinergic symptoms.

    2.5 Preparation of Infusion Solution

    Inspect vial contents for particulate matter and discoloration and repeat inspection when drug product is withdrawn from vial into syringe.

    CAMPTOSAR Injection 20 mg/mL is intended for single use only and any unused portion should be discarded.

    CAMPTOSAR Injection must be diluted prior to infusion. CAMPTOSAR should be diluted in 5% Dextrose Injection, USP, (preferred) or 0.9% Sodium Chloride Injection, USP, to a final concentration range of 0.12 mg/mL to 2.8 mg/mL. Other drugs should not be added to the infusion solution.

    The solution is physically and chemically stable for up to 24 hours at room temperature and in ambient fluorescent lighting. Solutions diluted in 5% Dextrose Injection, USP, and stored at refrigerated temperatures (approximately 2° to 8°C, 36° to 46°F), and protected from light are physically and chemically stable for 48 hours. Refrigeration of admixtures using 0.9% Sodium Chloride Injection, USP, is not recommended due to a low and sporadic incidence of visible particulates. Freezing CAMPTOSAR and admixtures of CAMPTOSAR may result in precipitation of the drug and should be avoided.

    The CAMPTOSAR Injection solution should be used immediately after reconstitution as it contains no antibacterial preservative. Because of possible microbial contamination during dilution, it is advisable to use the admixture prepared with 5% Dextrose Injection, USP, within 24 hours if refrigerated (2° to 8°C, 36° to 46°F). In the case of admixtures prepared with 5% Dextrose Injection, USP, or Sodium Chloride Injection, USP, the solutions should be used within 4 hours if kept at room temperature. If reconstitution and dilution are performed under strict aseptic conditions (e.g. on Laminar Air Flow bench), CAMPTOSAR Injection solution should be used (infusion completed) within 12 hours at room temperature or 24 hours if refrigerated (2° to 8°C, 36° to 46°F).

    2.6 Safe Handling

    Care should be exercised in the handling and preparation of infusion solutions prepared from CAMPTOSAR Injection. The use of gloves is recommended. If a solution of CAMPTOSAR contacts the skin, wash the skin immediately and thoroughly with soap and water. If CAMPTOSAR contacts the mucous membranes, flush thoroughly with water. Several published guidelines for handling and disposal of anticancer agents are available.

    2.7 Extravasation

    Care should be taken to avoid extravasation, and the infusion site should be monitored for signs of inflammation. Should extravasation occur, flushing the site with sterile water and applications of ice are recommended.

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  • 3 DOSAGE FORMS AND STRENGTHS

    CAMPTOSAR Injection is available in three single-dose sizes:

    • 2 mL-fill vial containing 40 mg irinotecan hydrochloride
    • 5 mL-fill vial containing 100 mg irinotecan hydrochloride
    • 15 mL-fill vial containing 300 mg irinotecan hydrochloride
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  • 4 CONTRAINDICATIONS

    • CAMPTOSAR Injection is contraindicated in patients with a known hypersensitivity to the drug or its excipients.
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  • 5 WARNINGS AND PRECAUTIONS

    5.1 Diarrhea and Cholinergic Reactions

    Early diarrhea (occurring during or shortly after infusion of CAMPTOSAR) is usually transient and infrequently severe. It may be accompanied by cholinergic symptoms of rhinitis, increased salivation, miosis, lacrimation, diaphoresis, flushing, and intestinal hyperperistalsis that can cause abdominal cramping. Bradycardia may also occur. Early diarrhea and other cholinergic symptoms may be prevented or treated. Consider prophylactic or therapeutic administration of 0.25 mg to 1 mg of intravenous or subcutaneous atropine (unless clinically contraindicated). These symptoms are expected to occur more frequently with higher irinotecan doses.

    Late diarrhea (generally occurring more than 24 hours after administration of CAMPTOSAR) can be life threatening since it may be prolonged and may lead to dehydration, electrolyte imbalance, or sepsis. Grade 3–4 late diarrhea occurred in 23–31% of patients receiving weekly dosing. In the clinical studies, the median time to the onset of late diarrhea was 5 days with 3-week dosing and 11 days with weekly dosing. Late diarrhea can be complicated by colitis, ulceration, bleeding, ileus, obstruction, and infection. Cases of megacolon and intestinal perforation have been reported. Patients should have loperamide readily available to begin treatment for late diarrhea. Begin loperamide at the first episode of poorly formed or loose stools or the earliest onset of bowel movements more frequent than normal. One dosage regimen for loperamide is 4 mg at the first onset of late diarrhea and then 2 mg every 2 hours until the patient is diarrhea-free for at least 12 hours. Loperamide is not recommended to be used for more than 48 consecutive hours at these doses, because of the risk of paralytic ileus. During the night, the patient may take 4 mg of loperamide every 4 hours. Monitor and replace fluid and electrolytes. Use antibiotic support for ileus, fever, or severe neutropenia. Subsequent weekly chemotherapy treatments should be delayed in patients until return of pretreatment bowel function for at least 24 hours without anti-diarrhea medication. Patients must not be treated with irinotecan until resolution of the bowel obstruction. If grade 2, 3, or 4 late diarrhea recurs, subsequent doses of CAMPTOSAR should be decreased [see Dosage and Administration (2)].

    Avoid diuretics or laxatives in patients with diarrhea.

    5.2 Myelosuppression

    Deaths due to sepsis following severe neutropenia have been reported in patients treated with CAMPTOSAR. In the clinical studies evaluating the weekly dosage schedule, neutropenic fever (concurrent NCI grade 4 neutropenia and fever of grade 2 or greater) occurred in 3% of the patients; 6% of patients received G-CSF for the treatment of neutropenia. Manage febrile neutropenia promptly with antibiotic support [see Warnings and Precautions (5.2)]. Hold CAMPTOSAR if neutropenic fever occurs or if the absolute neutrophil count drops <1000/mm3. After recovery to an absolute neutrophil count ≥1000/mm3, subsequent doses of CAMPTOSAR should be reduced [see Dosage and Administration (2)].

    When evaluated in the trials of weekly administration, the frequency of grade 3 and 4 neutropenia was higher in patients who received previous pelvic/abdominal irradiation than in those who had not received such irradiation (48% [13/27] versus 24% [67/277]; p=0.04). Patients who have previously received pelvic/abdominal irradiation are at increased risk of severe myelosuppression following the administration of CAMPTOSAR. Based on sparse available data, the concurrent administration of CAMPTOSAR with irradiation is not recommended.

    Patients with baseline serum total bilirubin levels of 1.0 mg/dL or more also had a greater likelihood of experiencing first-cycle grade 3 or 4 neutropenia than those with bilirubin levels that were less than 1.0 mg/dL (50% [19/38] versus 18% [47/266]; p<0.001). Patients with deficient glucuronidation of bilirubin, such as those with Gilbert's syndrome, may be at greater risk of myelosuppression when receiving therapy with CAMPTOSAR.

    5.3 Patients With Reduced UGT1A1 Activity

    Individuals who are homozygous for the UGT1A1*28 allele (UGT1A1 7/7 genotype) are at increased risk for neutropenia following initiation of CAMPTOSAR treatment.

    In a study of 66 patients who received single-agent CAMPTOSAR (350 mg/m2 once-every-3-weeks), the incidence of grade 4 neutropenia in patients homozygous for the UGT1A1*28 allele was 50%, and in patients heterozygous for this allele (UGT1A1 6/7 genotype) the incidence was 12.5%. No grade 4 neutropenia was observed in patients homozygous for the wild-type allele (UGT1A1 6/6 genotype).

    In a prospective study (n=250) to investigate the role of UGT1A1*28 polymorphism in the development of toxicity in patients treated with CAMPTOSAR (180 mg/m2) in combination with infusional 5-FU/LV, the incidence of grade 4 neutropenia in patients homozygous for the UGT1A1*28 allele was 4.5%, and in patients heterozygous for this allele the incidence was 5.3%. Grade 4 neutropenia was observed in 1.8% of patients homozygous for the wild-type allele.

    In another study in which 109 patients were treated with CAMPTOSAR (100–125 mg/m2) in combination with bolus 5-FU/LV, the incidence of grade 4 neutropenia in patients homozygous for the UGT1A1*28 allele was 18.2%, and in patients heterozygous for this allele the incidence was 11.1%. Grade 4 neutropenia was observed in 6.8% of patients homozygous for the wild-type allele.

    When administered in combination with other agents or as a single-agent, a reduction in the starting dose by at least one level of CAMPTOSAR should be considered for patients known to be homozygous for the UGT1A1*28 allele. However, the precise dose reduction in this patient population is not known and subsequent dose modifications should be considered based on individual patient tolerance to treatment [see Dosage and Administration (2)].

    UGT1A1 Testing

    A laboratory test is available to determine the UGT1A1 status of patients. Testing can detect the UGT1A1 6/6, 6/7 and 7/7 genotypes.

    5.4 Hypersensitivity

    Hypersensitivity reactions including severe anaphylactic or anaphylactoid reactions have been observed. Discontinue CAMPTOSAR if anaphylactic reaction occurs.

    5.5 Renal Impairment/Renal Failure

    Renal impairment and acute renal failure have been identified, usually in patients who became volume depleted from severe vomiting and/or diarrhea.

    5.6 Pulmonary Toxicity

    Interstitial Pulmonary Disease (IPD)-like events, including fatalities, have occurred in patients receiving irinotecan (in combination and as monotherapy). Risk factors include pre-existing lung disease, use of pneumotoxic drugs, radiation therapy, and colony stimulating factors. Patients with risk factors should be closely monitored for respiratory symptoms before and during irinotecan therapy. In Japanese studies, a reticulonodular pattern on chest x-ray was observed in a small percentage of patients. New or progressive, dyspnea, cough, and fever should prompt interruption of chemotherapy, pending diagnostic evaluation. If IPD is diagnosed, irinotecan and other chemotherapy should be discontinued and appropriate treatment instituted as needed [see Adverse Reactions (6.1)].

    5.7 Toxicity of the 5 Day Regimen

    Outside of a well-designed clinical study, CAMPTOSAR Injection should not be used in combination with a regimen of 5-FU/LV administered for 4–5 consecutive days every 4 weeks because of reports of increased toxicity, including toxic deaths. CAMPTOSAR should be used as recommended in Table 2 [see Dosage and Administration (2)].

    5.8 Increased Toxicity in Patients with Performance Status 2

    In patients receiving either irinotecan/5-FU/LV or 5-FU/LV in the clinical trials, higher rates of hospitalization, neutropenic fever, thromboembolism, first-cycle treatment discontinuation, and early deaths were observed in patients with a baseline performance status of 2 than in patients with a baseline performance status of 0 or 1.

    5.9 Pregnancy

    CAMPTOSAR can cause fetal harm when administered to a pregnant woman. Irinotecan was embryotoxic in rats and rabbits at doses significantly lower than those administered to humans on a mg/m2 basis. In rats, at exposures approximately 0.2 times those achieved in humans at the 125 mg/m2 dose, irinotecan was embryotoxic and resulted in decreased learning ability and female fetal body weight in surviving pups; the drug was teratogenic at lower exposures (approximately 0.025 times the AUC in humans at the 125 mg/m2 dose). There are no adequate and well-controlled studies of irinotecan in pregnant women. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to a fetus. Women of childbearing potential should be advised to avoid becoming pregnant while receiving treatment with CAMPTOSAR.

    5.10 Patients with Hepatic Impairment

    The use of CAMPTOSAR in patients with significant hepatic impairment has not been established. In clinical trials of either dosing schedule, irinotecan was not administered to patients with serum bilirubin >2.0 mg/dL, or transaminase >3 times the upper limit of normal if no liver metastasis, or transaminase >5 times the upper limit of normal with liver metastasis. In clinical trials of the weekly dosage schedule, patients with modestly elevated baseline serum total bilirubin levels (1.0 to 2.0 mg/dL) had a significantly greater likelihood of experiencing first-cycle, grade 3 or 4 neutropenia than those with bilirubin levels that were less than 1.0 mg/dL (50% [19/38] versus 18% [47/226]; p<0.001) [see Dosage and Administration (2.1), Use in Specific Populations (8.7) and Clinical Pharmacology (12.3)].

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  • 6 ADVERSE REACTIONS

    6.1 Clinical Studies Experience

    Because clinical trials are conducted under widely varying conditions, adverse reaction rates observed in the clinical trials of a drug cannot be directly compared to rates in the clinical trials of another drug and may not reflect the rates observed in clinical practice.

    Common adverse reactions (≥30%) observed in combination therapy clinical studies are: nausea, vomiting, abdominal pain, diarrhea, constipation, anorexia, mucositis, neutropenia, leukopenia (including lymphocytopenia), anemia, thrombocytopenia, asthenia, pain, fever, infection, abnormal bilirubin, and alopecia.

    Common adverse reactions (≥30%) observed in single agent therapy clinical studies are: nausea, vomiting, abdominal pain, diarrhea, constipation, anorexia, neutropenia, leukopenia (including lymphocytopenia), anemia, asthenia, fever, body weight decreasing, and alopecia.

    Serious opportunistic infections have not been observed, and no complications have specifically been attributed to lymphocytopenia.

    First-Line Combination Therapy

    A total of 955 patients with metastatic colorectal cancer received the recommended regimens of irinotecan in combination with 5-FU/LV, 5-FU/LV alone, or irinotecan alone. In the two phase 3 studies, 370 patients received irinotecan in combination with 5-FU/LV, 362 patients received 5-FU/LV alone, and 223 patients received irinotecan alone [see Dosage and Administration (2)].

    In Study 1, 49 (7.3%) patients died within 30 days of last study treatment: 21 (9.3%) received irinotecan in combination with 5-FU/LV, 15 (6.8%) received 5-FU/LV alone, and 13 (5.8%) received irinotecan alone. Deaths potentially related to treatment occurred in 2 (0.9%) patients who received irinotecan in combination with 5-FU/LV (2 neutropenic fever/sepsis), 3 (1.4%) patients who received 5-FU/LV alone (1 neutropenic fever/sepsis, 1 CNS bleeding during thrombocytopenia, 1 unknown) and 2 (0.9%) patients who received irinotecan alone (2 neutropenic fever). Deaths from any cause within 60 days of first study treatment were reported for 15 (6.7%) patients who received irinotecan in combination with 5-FU/LV, 16 (7.3%) patients who received 5-FU/LV alone, and 15 (6.7%) patients who received irinotecan alone. Discontinuations due to adverse events were reported for 17 (7.6%) patients who received irinotecan in combination with 5FU/LV, 14 (6.4%) patients who received 5-FU/LV alone, and 26 (11.7%) patients who received irinotecan alone.

    In Study 2, 10 (3.5%) patients died within 30 days of last study treatment: 6 (4.1%) received irinotecan in combination with 5-FU/LV and 4 (2.8%) received 5-FU/LV alone. There was one potentially treatment-related death, which occurred in a patient who received irinotecan in combination with 5-FU/LV (0.7%, neutropenic sepsis). Deaths from any cause within 60 days of first study treatment were reported for 3 (2.1%) patients who received irinotecan in combination with 5-FU/LV and 2 (1.4%) patients who received 5-FU/LV alone. Discontinuations due to adverse events were reported for 9 (6.2%) patients who received irinotecan in combination with 5FU/LV and 1 (0.7%) patient who received 5-FU/LV alone.

    The most clinically significant adverse events for patients receiving irinotecan-based therapy were diarrhea, nausea, vomiting, neutropenia, and alopecia. The most clinically significant adverse events for patients receiving 5-FU/LV therapy were diarrhea, neutropenia, neutropenic fever, and mucositis. In Study 1, grade 4 neutropenia, neutropenic fever (defined as grade 2 fever and grade 4 neutropenia), and mucositis were observed less often with weekly irinotecan/5-FU/LV than with monthly administration of 5-FU/LV.

    Tables 5 and 6 list the clinically relevant adverse events reported in Studies 1 and 2, respectively.

    Table 5. Study 1: Percent (%) of Patients Experiencing Clinically Relevant Adverse Events in Combination Therapies*
    Adverse Event Study 1
    Irinotecan + Bolus 5-FU/LV weekly × 4 every 6 weeks
    N=225
    Bolus 5-FU/LV daily × 5 every 4 weeks
    N=219
    Irinotecan weekly × 4 every 6 weeks
    N=223
    Grade 1–4 Grade 3&4 Grade 1–4 Grade 3&4 Grade 1–4 Grade 3&4
    *
    Severity of adverse events based on NCI CTC (version 1.0)
    Complete hair loss = Grade 2
    Includes angina pectoris, arterial thrombosis, cerebral infarct, cerebrovascular accident, deep thrombophlebitis, embolus lower extremity, heart arrest, myocardial infarct, myocardial ischemia, peripheral vascular disorder, pulmonary embolus, sudden death, thrombophlebitis, thrombosis, vascular disorder.
    TOTAL Adverse Events 100 53.3 100 45.7 99.6 45.7
    GASTROINTESTINAL
      Diarrhea 84.9 22.7 69.4 13.2 83.0 31.0
        late -- 15.1 -- 5.9 -- 18.4
          grade 3 -- 7.6 -- 7.3 -- 12.6
          grade 4
        early
    45.8 4.9 31.5 1.4 43.0 6.7
      Nausea 79.1 15.6 67.6 8.2 81.6 16.1
      Abdominal pain 63.1 14.6 50.2 11.5 67.7 13.0
      Vomiting 60.4 9.7 46.1 4.1 62.8 12.1
      Anorexia 34.2 5.8 42.0 3.7 43.9 7.2
      Constipation 41.3 3.1 31.5 1.8 32.3 0.4
      Mucositis 32.4 2.2 76.3 16.9 29.6 2.2
    HEMATOLOGIC
      Neutropenia 96.9 53.8 98.6 66.7 96.4 31.4
        grade 3 -- 29.8 -- 23.7 -- 19.3
        grade 4 -- 24.0 -- 42.5 -- 12.1
      Leukopenia 96.9 37.8 98.6 23.3 96.4 21.5
      Anemia 96.9 8.4 98.6 5.5 96.9 4.5
      Neutropenic fever -- 7.1 -- 14.6 -- 5.8
      Thrombocytopenia 96.0 2.6 98.6 2.7 96.0 1.7
      Neutropenic infection -- 1.8 -- 0 -- 2.2
    BODY AS A WHOLE
      Asthenia 70.2 19.5 64.4 11.9 69.1 13.9
      Pain 30.7 3.1 26.9 3.6 22.9 2.2
      Fever 42.2 1.7 32.4 3.6 43.5 0.4
      Infection 22.2 0 16.0 1.4 13.9 0.4
    METABOLIC & NUTRITIONAL
      Bilirubin 87.6 7.1 92.2 8.2 83.9 7.2
    DERMATOLOGIC 0.9 0 3.2 0.5 0 0
      Exfoliative dermatitis 19.1 0 26.5 0.9 14.3 0.4
      Rash
      Alopecia
    43.1 -- 26.5 -- 46.1 --
    RESPIRATORY
      Dyspnea 27.6 6.3 16.0 0.5 22.0 2.2
      Cough 26.7 1.3 18.3 0 20.2 0.4
      Pneumonia 6.2 2.7 1.4 1.0 3.6 1.3
    NEUROLOGIC
      Dizziness 23.1 1.3 16.4 0 21.1 1.8
      Somnolence 12.4 1.8 4.6 1.8 9.4 1.3
      Confusion 7.1 1.8 4.1 0 2.7 0
    CARDIOVASCULAR 9.3 0.9 5.0 0 9.0 0
      Vasodilatation 5.8 1.3 2.3 0.5 5.8 1.7
      Hypotension
      Thromboembolic events
    9.3 -- 11.4 -- 5.4 --
    Table 6. Study 2: Percent (%) of Patients Experiencing Clinically Relevant Adverse Events in Combination Therapies*
    Adverse Event Study 2
    Irinotecan + 5-FU/LV infusional days 1&2 every 2 weeks
    N= 145
    5-FU/LV infusional days 1&2 every 2 weeks
    N=143
    Grades 1–4 Grades 3&4 Grades 1–4 Grades 3&4
    *
    Severity of adverse events based on NCI CTC (version 1.0)
    Includes rhinitis, increased salivation, miosis, lacrimation, diaphoresis, flushing, abdominal cramping or diarrhea (occurring during or shortly after infusion of irinotecan)
    Complete hair loss = Grade 2
    §
    Includes angina pectoris, arterial thrombosis, cerebral infarct, cerebrovascular accident, deep thrombophlebitis, embolus lower extremity, heart arrest, myocardial infarct, myocardial ischemia, peripheral vascular disorder, pulmonary embolus, sudden death, thrombophlebitis, thrombosis, vascular disorder.
    TOTAL Adverse Events 100 72.4 100 39.2
    GASTROINTESTINAL
      Diarrhea 72.4 14.4 44.8 6.3
        late -- 10.3 -- 4.2
          grade 3 -- 4.1 -- 2.1
          grade 4
      Cholinergic syndrome
    28.3 1.4 0.7 0
      Nausea 66.9 2.1 55.2 3.5
      Abdominal pain 17.2 2.1 16.8 0.7
      Vomiting 44.8 3.5 32.2 2.8
      Anorexia 35.2 2.1 18.9 0.7
      Constipation 30.3 0.7 25.2 1.4
      Mucositis 40.0 4.1 28.7 2.8
    HEMATOLOGIC
      Neutropenia 82.5 46.2 47.9 13.4
        grade 3 -- 36.4 -- 12.7
        grade 4 -- 9.8 -- 0.7
      Leukopenia 81.3 17.4 42.0 3.5
      Anemia 97.2 2.1 90.9 2.1
      Neutropenic fever -- 3.4 -- 0.7
      Thrombocytopenia 32.6 0 32.2 0
      Neutropenic infection -- 2.1 -- 0
    BODY AS A WHOLE
      Asthenia 57.9 9.0 48.3 4.2
      Pain 64.1 9.7 61.5 8.4
      Fever 22.1 0.7 25.9 0.7
      Infection 35.9 7.6 33.6 3.5
    METABOLIC AND NUTRITIONAL
      Bilirubin 19.1 3.5 35.9 10.6
    DERMATOLOGIC 10.3 0.7 12.6 0.7
      Hand and foot syndrome 17.2 0.7 20.3 0
      Cutaneous signs
      Alopecia
    56.6 -- 16.8 --
    RESPIRATORY
      Dyspnea 9.7 1.4 4.9 0
    CARDIOVASCULAR 3.4 1.4 0.7 0
      Hypotension
      Thromboembolic events§
    11.7 -- 5.6 --

    Second-Line Single-Agent Therapy

    Weekly Dosage Schedule

    In three clinical studies evaluating the weekly dosage schedule, 304 patients with metastatic carcinoma of the colon or rectum that had recurred or progressed following 5-FU-based therapy were treated with CAMPTOSAR. Seventeen of the patients died within 30 days of the administration of CAMPTOSAR; in five cases (1.6%, 5/304), the deaths were potentially drug-related. One of the patients died of neutropenic sepsis without fever. Neutropenic fever occurred in nine (3.0%) other patients; these patients recovered with supportive care.

    One hundred nineteen (39.1%) of the 304 patients were hospitalized because of adverse events; 81 (26.6%) patients were hospitalized for events judged to be related to administration of CAMPTOSAR. The primary reasons for drug-related hospitalization were diarrhea, with or without nausea and/or vomiting (18.4%); neutropenia/leukopenia, with or without diarrhea and/or fever (8.2%); and nausea and/or vomiting (4.9%).

    The first dose of at least one cycle of CAMPTOSAR was reduced for 67% of patients who began the studies at the 125-mg/m2 starting dose. Within-cycle dose reductions were required for 32% of the cycles initiated at the 125-mg/m2 dose level. The most common reasons for dose reduction were late diarrhea, neutropenia, and leukopenia. Thirteen (4.3%) patients discontinued treatment with CAMPTOSAR because of adverse events. The adverse events in Table 7 are based on the experience of the 304 patients enrolled in the three studies described in CLINICAL STUDIES (14.1).

    Table 7. Adverse Events Occurring in >10% of 304 Previously Treated Patients with Metastatic Carcinoma of the Colon or Rectum*
    % of Patients Reporting
    Body System & Event NCI Grades 1–4 NCI Grades 3 & 4
    *
    Severity of adverse events based on NCI CTC (version 1.0)
    Occurring > 24 hours after administration of CAMPTOSAR
    Occurring ≤24 hours after administration of CAMPTOSAR
    §
    Primarily upper respiratory infections
    Not applicable; complete hair loss = NCI grade 2
    GASTROINTESTINAL
      Diarrhea (late) 88 31
        7–9 stools/day (grade 3) (16)
        ≥10 stools/day (grade 4) (14)
      Nausea 86 17
      Vomiting 67 12
      Anorexia 55 6
      Diarrhea (early) 51 8
      Constipation 30 2
      Flatulence 12 0
      Stomatitis 12 1
      Dyspepsia 10 0
    HEMATOLOGIC
      Leukopenia 63 28
      Anemia 60 7
      Neutropenia 54 26
        500 to <1000/mm3 (grade 3) (15)
        <500/mm3 (grade 4) (12)
    BODY AS A WHOLE
      Asthenia 76 12
      Abdominal cramping/pain 57 16
      Fever 45 1
      Pain 24 2
      Headache 17 1
      Back pain 14 2
      Chills 14 0
      Minor infection§ 14 0
      Edema 10 1
      Abdominal enlargement 10 0
    METABOLIC AND NUTRITIONAL
      ↓ Body weight 30 1
      Dehydration 15 4
      ↑ Alkaline phosphatase 13 4
      ↑ SGOT 10 1
    DERMATOLOGIC
      Alopecia 60 NA
      Sweating 16 0
      Rash 13 1
    RESPIRATORY
      Dyspnea 22 4
      ↑ Coughing 17 0
      Rhinitis 16 0
    NEUROLOGIC
      Insomnia 19 0
      Dizziness 15 0
    CARDIOVASCULAR
      Vasodilation (flushing) 11 0

    Once-Every-3-Week Dosage Schedule

    A total of 535 patients with metastatic colorectal cancer whose disease had recurred or progressed following prior 5-FU therapy participated in the two phase 3 studies: 316 received irinotecan, 129 received 5-FU, and 90 received best supportive care. Eleven (3.5%) patients treated with irinotecan died within 30 days of treatment. In three cases (1%, 3/316), the deaths were potentially related to irinotecan treatment and were attributed to neutropenic infection, grade 4 diarrhea, and asthenia, respectively. One (0.8%, 1/129) patient treated with 5-FU died within 30 days of treatment; this death was attributed to grade 4 diarrhea.

    Hospitalizations due to serious adverse events occurred at least once in 60% (188/316) of patients who received irinotecan, 63% (57/90) who received best supportive care, and 39% (50/129) who received 5-FU-based therapy. Eight percent of patients treated with irinotecan and 7% treated with 5-FU-based therapy discontinued treatment due to adverse events.

    Of the 316 patients treated with irinotecan, the most clinically significant adverse events (all grades, 1–4) were diarrhea (84%), alopecia (72%), nausea (70%), vomiting (62%), cholinergic symptoms (47%), and neutropenia (30%). Table 8 lists the grade 3 and 4 adverse events reported in the patients enrolled to all treatment arms of the two studies described in CLINICAL STUDIES (14.1).

    Table 8: Percent Of Patients Experiencing Grade 3 & 4 Adverse Events In Comparative Studies Of Once-Every-3-Week Irinotecan Therapy*
    Study 1 Study 2
    Adverse Event Irinotecan
    N=189
    BSC
    N=90
    Irinotecan
    N=127
    5-FU
    N=129
    *
    Severity of adverse events based on NCI CTC (version 1.0)
    BSC = best supportive care
    Hepatic includes events such as ascites and jaundice
    §
    Cutaneous signs include events such as rash
    Respiratory includes events such as dyspnea and cough
    #
    Neurologic includes events such as somnolence
    Þ
    Cardiovascular includes events such as dysrhythmias, ischemia, and mechanical cardiac dysfunction
    ß
    Other includes events such as accidental injury, hepatomegaly, syncope, vertigo, and weight loss
    TOTAL Grade 3/4
    Adverse Events
    79 67 69 54
    GASTROINTESTINAL
      Diarrhea 22 6 22 11
      Vomiting 14 8 14 5
      Nausea 14 3 11 4
      Abdominal pain 14 16 9 8
      Constipation 10 8 8 6
      Anorexia 5 7 6 4
      Mucositis 2 1 2 5
    HEMATOLOGIC
      Leukopenia/Neutropenia 22 0 14 2
      Anemia 7 6 6 3
      Hemorrhage 5 3 1 3
      Thrombocytopenia 1 0 4 2
    Infection
      without grade 3/4 neutropenia 8 3 1 4
      with grade 3/4 neutropenia 1 0 2 0
    Fever
      without grade 3/4 neutropenia 2 1 2 0
      with grade 3/4 neutropenia 2 0 4 2
    BODY AS A WHOLE
      Pain 19 22 17 13
      Asthenia 15 19 13 12
    METABOLIC AND NUTRITIONAL
    Hepatic 9 7 9 6
    DERMATOLOGIC
      Hand and foot syndrome 0 0 0 5
      Cutaneous signs § 2 0 1 3
    RESPIRATORY 10 8 5 7
    NEUROLOGIC# 12 13 9 4
    CARDIOVASCULARÞ 9 3 4 2
    OTHERß 32 28 12 14

    The incidence of akathisia in clinical trials of the weekly dosage schedule was greater (8.5%, 4/47 patients) when prochlorperazine was administered on the same day as CAMPTOSAR than when these drugs were given on separate days (1.3%, 1/80 patients). The 8.5% incidence of akathisia, however, is within the range reported for use of prochlorperazine when given as a premedication for other chemotherapies.

    6.2 Postmarketing Experience

    The following adverse reactions have been identified during post approval use of CAMPTOSAR. Because these reactions are reported voluntarily from a population of uncertain size, it is not always possible to reliably estimate their frequency or establish a causal relationship to drug exposure.

    Myocardial ischemic events have been observed following irinotecan therapy. Thromboembolic events have been observed in patients receiving CAMPTOSAR.

    Symptomatic pancreatitis, asymptomatic pancreatic enzyme elevation have been reported. Increases in serum levels of transaminases (i.e., AST and ALT) in the absence of progressive liver metastasis have been observed.

    Hyponatremia, mostly with diarrhea and vomiting, has been reported.

    Transient dysarthria has been reported in patients treated with CAMPTOSAR; in some cases, the event was attributed to the cholinergic syndrome observed during or shortly after infusion of irinotecan.

    Interaction between irinotecan and neuromuscular blocking agents cannot be ruled out. Irinotecan has anticholinesterase activity, which may prolong the neuromuscular blocking effects of suxamethonium and the neuromuscular blockade of non-depolarizing drugs may be antagonized.

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  • 7 DRUG INTERACTIONS

    7.1 5-Fluorouracil (5-FU) and Leucovorin (LV)

    In a phase 1 clinical study involving irinotecan, 5-fluorouracil (5-FU), and leucovorin (LV) in 26 patients with solid tumors, the disposition of irinotecan was not substantially altered when the drugs were co-administered. Although the Cmax and AUC0–24 of SN-38, the active metabolite, were reduced (by 14% and 8%, respectively) when irinotecan was followed by 5-FU and LV administration compared with when irinotecan was given alone, this sequence of administration was used in the combination trials and is recommended [see Dosage and Administration (2)]. Formal in vivo or in vitro drug interaction studies to evaluate the influence of irinotecan on the disposition of 5-FU and LV have not been conducted.

    7.2 Strong CYP 3A4 Inducers

    Anticonvulsants and other strong inducers: Exposure to irinotecan and its active metabolite SN-38 is substantially reduced in adult and pediatric patients concomitantly receiving the CYP3A4 enzyme-inducing anticonvulsants phenytoin, phenobarbital or carbamazepine. The appropriate starting dose for patients taking these anticonvulsants or other strong inducers such as rifampin and rifabutin has not been defined. Consideration should be given to substituting non-enzyme inducing therapies at least 2 weeks prior to initiation of irinotecan therapy.

    St. John's wort: Exposure to the active metabolite SN-38 is reduced in patients receiving concomitant St. John's wort. St. John's wort should be discontinued at least 2 weeks prior to the first cycle of irinotecan, and St. John's wort is contraindicated during irinotecan therapy.

    Dexamethasone, a moderate CYP3A4 inducer, does not appear to alter the pharmacokinetics of irinotecan.

    7.3 Strong CYP 3A4 Inhibitors

    Ketoconazole is a strong inhibitor of CYP3A4 enzymes. Patients receiving concomitant ketoconazole have increased exposure to irinotecan and its active metabolite SN-38. Patients should discontinue ketoconazole at least 1 week prior to starting irinotecan therapy and ketoconazole is contraindicated during irinotecan therapy.

    7.4 Atazanavir Sulfate

    Coadministration of atazanavir sulfate, a CYP3A4 and UGT1A1 inhibitor has the potential to increase systemic exposure to SN-38, the active metabolite of irinotecan. Physicians should take this into consideration when co-administering these drugs.

    7.5 Drug-Laboratory Test Interactions

    There are no known interactions between CAMPTOSAR and laboratory tests.

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  • 8 USE IN SPECIFIC POPULATIONS

    8.1 Pregnancy

    Pregnancy Category D [see Warnings and Precautions (5.9)]

    CAMPTOSAR can cause fetal harm when administered to a pregnant woman. Radioactivity related to 14C-irinotecan crosses the placenta of rats following intravenous administration of 10 mg/kg (which in separate studies produced an irinotecan Cmax and AUC about 3 and 0.5 times, respectively, the corresponding values in patients administered 125 mg/m2). Intravenous administration of irinotecan 6 mg/kg/day to rats and rabbits during the period of organogenesis resulted in increased post-implantation loss and decreased numbers of live fetuses. In separate studies in rats, this dose produced an irinotecan Cmax and AUC of about 2 and 0.2 times, respectively, the corresponding values in patients administered 125 mg/m2. In rabbits, the embryotoxic dose was about one-half the recommended human weekly starting dose on a mg/m2 basis. Irinotecan was teratogenic in rats at doses greater than 1.2 mg/kg/day and in rabbits at 6.0 mg/kg/day. In separate studies in rats, this dose produced an irinotecan Cmax and AUC about 2/3 and 1/40th, respectively, of the corresponding values in patients administered 125 mg/m2. In rabbits, the teratogenic dose was about one-half the recommended human weekly starting dose on a mg/m2 basis. Teratogenic effects included a variety of external, visceral, and skeletal abnormalities. Irinotecan administered to rat dams for the period following organogenesis through weaning at doses of 6 mg/kg/day caused decreased learning ability and decreased female body weights in the offspring. There are no adequate and well-controlled studies of irinotecan in pregnant women. If this drug is used during pregnancy, or if the patient becomes pregnant while taking this drug, the patient should be apprised of the potential hazard to a fetus. Women of childbearing potential should be advised to avoid becoming pregnant while receiving treatment with CAMPTOSAR.

    8.3 Nursing Mothers

    Radioactivity appeared in rat milk within 5 minutes of intravenous administration of radiolabeled irinotecan and was concentrated up to 65-fold at 4 hours after administration relative to plasma concentrations. It is not known whether this drug is excreted in human milk. Because many drugs are excreted in human milk and because of the potential for serious adverse reactions in nursing infants from CAMPTOSAR, a decision should be made whether to discontinue nursing or discontinue the drug, taking into account the importance of the drug to the mother.

    8.4 Pediatric Use

    The effectiveness of irinotecan in pediatric patients has not been established. Results from two open-label, single arm studies were evaluated. One hundred and seventy children with refractory solid tumors were enrolled in one phase 2 trial in which 50 mg/ m2 of irinotecan was infused for 5 consecutive days every 3 weeks. Grade 3–4 neutropenia was experienced by 54 (31.8%) patients. Neutropenia was complicated by fever in 15 (8.8%) patients. Grade 3–4 diarrhea was observed in 35 (20.6%) patients. This adverse event profile was comparable to that observed in adults. In the second phase 2 trial of 21 children with previously untreated rhabdomyosarcoma, 20 mg/m2 of irinotecan was infused for 5 consecutive days on weeks 0, 1, 3 and 4. This single agent therapy was followed by multimodal therapy. Accrual to the single agent irinotecan phase was halted due to the high rate (28.6%) of progressive disease and the early deaths (14%). The adverse event profile was different in this study from that observed in adults; the most significant grade 3 or 4 adverse events were dehydration experienced by 6 patients (28.6%) associated with severe hypokalemia in 5 patients (23.8%) and hyponatremia in 3 patients (14.3%); in addition Grade 3–4 infection was reported in 5 patients (23.8%) (across all courses of therapy and irrespective of causal relationship).

    Pharmacokinetic parameters for irinotecan and SN-38 were determined in 2 pediatric solid-tumor trials at dose levels of 50 mg/m2 (60-min infusion, n=48) and 125 mg/m2 (90-min infusion, n=6). Irinotecan clearance (mean ± S.D.) was 17.3 ± 6.7 L/h/m2 for the 50mg/m2 dose and 16.2 ± 4.6 L/h/m2 for the 125 mg/m2 dose, which is comparable to that in adults. Dose-normalized SN-38 AUC values were comparable between adults and children. Minimal accumulation of irinotecan and SN-38 was observed in children on daily dosing regimens [daily × 5 every 3 weeks or (daily × 5) × 2 weeks every 3 weeks].

    8.5 Geriatric Use

    Patients greater than 65 years of age should be closely monitored because of a greater risk of early and late diarrhea in this population [see Clinical Pharmacology (12.3) and Adverse Reactions (6.1)]. The starting dose of CAMPTOSAR in patients 70 years and older for the once-every-3-week-dosage schedule should be 300 mg/m2 [see Clinical Pharmacology (12.3) and Dosage and Administration (2)].

    The frequency of grade 3 and 4 late diarrhea by age was significantly greater in patients ≥65 years than in patients <65 years (40% [53/133] versus 23% [40/171]; p=0.002). In another study of 183 patients treated on the weekly schedule, the frequency of grade 3 or 4 late diarrhea in patients ≥65 years of age was 28.6% [26/91] and in patients <65 years of age was 23.9% [22/92].

    8.6 Renal Impairment

    The influence of renal impairment on the pharmacokinetics of irinotecan has not been evaluated. Therefore, use caution in patients with impaired renal function. Irinotecan is not recommended for use in patients on dialysis.

    8.7 Hepatic Impairment

    Irinotecan clearance is diminished in patients with hepatic impairment while exposure to the active metabolite SN-38 is increased relative to that in patients with normal hepatic function. The magnitude of these effects is proportional to the degree of liver impairment as measured by elevations in total bilirubin and transaminase concentrations. Therefore, use caution in patients with hepatic impairment. The tolerability of irinotecan in patients with hepatic dysfunction (bilirubin greater than 2 mg/dl) has not been assessed sufficiently, and no recommendations for dosing can be made [see Dosage and Administration (2.1), Warnings and Precautions (5.10) and Clinical Pharmacology (12.3)].

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  • 10 OVERDOSAGE

    In U.S. phase 1 trials, single doses of up to 345 mg/m2 of irinotecan were administered to patients with various cancers. Single doses of up to 750 mg/m2 of irinotecan have been given in non-U.S. trials. The adverse events in these patients were similar to those reported with the recommended dosage and regimen. There have been reports of overdosage at doses up to approximately twice the recommended therapeutic dose, which may be fatal. The most significant adverse reactions reported were severe neutropenia and severe diarrhea. There is no known antidote for overdosage of CAMPTOSAR. Maximum supportive care should be instituted to prevent dehydration due to diarrhea and to treat any infectious complications.

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  • 11 DESCRIPTION

    CAMPTOSAR Injection (irinotecan hydrochloride injection) is an antineoplastic agent of the topoisomerase I inhibitor class.

    CAMPTOSAR is supplied as a sterile, pale yellow, clear, aqueous solution. Each milliliter of solution contains 20 mg of irinotecan hydrochloride (on the basis of the trihydrate salt), 45 mg of sorbitol, NF, and 0.9 mg of lactic acid, USP. The pH of the solution has been adjusted to 3.5 (range, 3.0 to 3.8) with sodium hydroxide or hydrochloric acid. CAMPTOSAR is intended for dilution with 5% Dextrose Injection, USP (D5W), or 0.9% Sodium Chloride Injection, USP, prior to intravenous infusion. The preferred diluent is 5% Dextrose Injection, USP.

    Irinotecan hydrochloride is a semisynthetic derivative of camptothecin, an alkaloid extract from plants such as Camptotheca acuminata or is chemically synthesized.

    The chemical name is (S)-4,11-diethyl-3,4,12,14-tetrahydro-4-hydroxy-3,14-dioxo1H-pyrano[3',4':6,7]-indolizino[1,2-b]quinolin-9-yl-[1,4'bipiperidine]-1'-carboxylate, monohydrochloride, trihydrate. Its empirical formula is C33H38N4O6•HCl•3H2O and molecular weight is 677.19. It is slightly soluble in water and organic solvents. Its structural formula is as follows:

    Chemical Structure
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  • 12 CLINICAL PHARMACOLOGY

    12.1 Mechanism of Action

    Irinotecan is a derivative of camptothecin. Camptothecins interact specifically with the enzyme topoisomerase I, which relieves torsional strain in DNA by inducing reversible single-strand breaks. Irinotecan and its active metabolite SN-38 bind to the topoisomerase I-DNA complex and prevent religation of these single-strand breaks. Current research suggests that the cytotoxicity of irinotecan is due to double-strand DNA damage produced during DNA synthesis when replication enzymes interact with the ternary complex formed by topoisomerase I, DNA, and either irinotecan or SN-38. Mammalian cells cannot efficiently repair these double-strand breaks.

    12.2 Pharmacodynamics

    Irinotecan serves as a water-soluble precursor of the lipophilic metabolite SN-38. SN-38 is formed from irinotecan by carboxylesterase-mediated cleavage of the carbamate bond between the camptothecin moiety and the dipiperidino side chain. SN-38 is approximately 1000 times as potent as irinotecan as an inhibitor of topoisomerase I purified from human and rodent tumor cell lines. In vitro cytotoxicity assays show that the potency of SN-38 relative to irinotecan varies from 2- to 2000-fold; however, the plasma area under the concentration versus time curve (AUC) values for SN-38 are 2% to 8% of irinotecan and SN-38 is 95% bound to plasma proteins compared to approximately 50% bound to plasma proteins for irinotecan [see Clinical Pharmacology (12.3)]. The precise contribution of SN-38 to the activity of CAMPTOSAR is thus unknown. Both irinotecan and SN-38 exist in an active lactone form and an inactive hydroxy acid anion form. A pH-dependent equilibrium exists between the two forms such that an acid pH promotes the formation of the lactone, while a more basic pH favors the hydroxy acid anion form.

    Administration of irinotecan has resulted in antitumor activity in mice bearing cancers of rodent origin and in human carcinoma xenografts of various histological types.

    12.3 Pharmacokinetics

    After intravenous infusion of irinotecan in humans, irinotecan plasma concentrations decline in a multiexponential manner, with a mean terminal elimination half-life of about 6 to 12 hours. The mean terminal elimination half-life of the active metabolite SN-38 is about 10 to 20 hours. The half-lives of the lactone (active) forms of irinotecan and SN-38 are similar to those of total irinotecan and SN-38, as the lactone and hydroxy acid forms are in equilibrium.

    Over the recommended dose range of 50 to 350 mg/m2, the AUC of irinotecan increases linearly with dose; the AUC of SN-38 increases less than proportionally with dose. Maximum concentrations of the active metabolite SN-38 are generally seen within 1 hour following the end of a 90-minute infusion of irinotecan. Pharmacokinetic parameters for irinotecan and SN-38 following a 90-minute infusion of irinotecan at dose levels of 125 and 340 mg/m2 determined in two clinical studies in patients with solid tumors are summarized in Table 9:

    Table 9. Summary of Mean (±Standard Deviation) Irinotecan and SN-38 Pharmacokinetic Parameters in Patients with Solid Tumors
    Dose
    (mg/m2)
    Irinotecan SN-38
    Cmax
    (ng/mL)
    AUC0–24
    (ng∙h/mL)
    t1/2
    (h)
    Vz
    (L/m2)
    CL
    (L/h/m2)
    Cmax
    (ng/mL)
    AUC0–24
    (ng∙h/mL)
    t1/2
    (h)
    Cmax - Maximum plasma concentration
    AUC0–24 - Area under the plasma concentration-time curve from time
    0 to 24 hours after the end of the 90-minute infusion
    t1/2 - Terminal elimination half-life
    Vz - Volume of distribution of terminal elimination phase
    CL - Total systemic clearance
    *
    Plasma specimens collected for 24 hours following the end of the 90-minute infusion.
    Plasma specimens collected for 48 hours following the end of the 90-minute infusion. Because of the longer collection period, these values provide a more accurate reflection of the terminal elimination half-lives of irinotecan and SN-38.
    125
    (N=64)
    1,660
    ±797
    10,200
    ±3,270
    5.8*
    ±0.7
    110
    ±48.5
    13.3
    ±6.01
    26.3
    ±11.9
    229
    ±108
    10.4*
    ±3.1
    340
    (N=6)
    3,392
    ±874
    20,604
    ±6,027
    11.7
    ±1.0
    234
    ±69.6
    13.9
    ±4.0
    56.0
    ±28.2
    474
    ±245
    21.0
    ±4.3

    Distribution

    Irinotecan exhibits moderate plasma protein binding (30% to 68% bound). SN-38 is highly bound to human plasma proteins (approximately 95% bound). The plasma protein to which irinotecan and SN-38 predominantly binds is albumin.

    Metabolism

    The metabolic conversion of irinotecan to the active metabolite SN-38 is mediated by carboxylesterase enzymes and primarily occurs in the liver. In vitro studies indicate that irinotecan, SN-38 and another metabolite aminopentane carboxylic acid (APC), do not inhibit cytochrome P-450 isozymes. SN-38 is subsequently conjugated predominantly by the enzyme UDP-glucuronosyl transferase 1A1 (UGT1A1) to form a glucuronide metabolite. UGT1A1 activity is reduced in individuals with genetic polymorphisms that lead to reduced enzyme activity such as the UGT1A1*28 polymorphism. Approximately 10% of the North American population is homozygous for the UGT1A1*28 allele (also referred to as UGT1A1 7/7 genotype). In a prospective study, in which irinotecan was administered as a single-agent (350 mg/m2) on a once-every-3-week schedule, patients with the UGT1A1 7/7 genotype had a higher exposure to SN-38 than patients with the wild-type UGT1A1 allele (UGT1A1 6/6 genotype) [see Warnings and Precautions (5.3) and Dosage and Administration (2)]. SN-38 glucuronide had 1/50 to 1/100 the activity of SN-38 in cytotoxicity assays using two cell lines in vitro.

    Excretion

    The disposition of irinotecan has not been fully elucidated in humans. The urinary excretion of irinotecan is 11% to 20%; SN-38, <1%; and SN-38 glucuronide, 3%. The cumulative biliary and urinary excretion of irinotecan and its metabolites (SN-38 and SN-38 glucuronide) over a period of 48 hours following administration of irinotecan in two patients ranged from approximately 25% (100 mg/m2) to 50% (300 mg/m2).

    Effect of Age

    The pharmacokinetics of irinotecan administered using the weekly schedule was evaluated in a study of 183 patients that was prospectively designed to investigate the effect of age on irinotecan toxicity. Results from this trial indicate that there are no differences in the pharmacokinetics of irinotecan, SN-38, and SN-38 glucuronide in patients <65 years of age compared with patients ≥65 years of age. In a study of 162 patients that was not prospectively designed to investigate the effect of age, small (less than 18%) but statistically significant differences in dose-normalized irinotecan pharmacokinetic parameters in patients <65 years of age compared to patients ≥65 years of age were observed. Although dose-normalized AUC0–24 for SN-38 in patients ≥65 years of age was 11% higher than in patients <65 years of age, this difference was not statistically significant. No change in the starting dose is recommended for geriatric patients receiving the weekly dosage schedule of irinotecan [see Dosage and Administration (2)].

    Effect of Gender

    The pharmacokinetics of irinotecan do not appear to be influenced by gender.

    Effect of Race

    The influence of race on the pharmacokinetics of irinotecan has not been evaluated.

    Effect of Hepatic Impairment

    Irinotecan clearance is diminished in patients with hepatic impairment while exposure to the active metabolite SN-38 is increased relative to that in patients with normal hepatic function. The magnitude of these effects is proportional to the degree of liver impairment as measured by elevations in total bilirubin and transaminase concentrations. However, the tolerability of irinotecan in patients with hepatic dysfunction (bilirubin greater than 2 mg/dl) has not been assessed sufficiently, and no recommendations for dosing can be made [see Dosage and Administration (2.1), Warnings and Precautions (5.10) and Use in Specific Populations (8.7)].

    Effect of Renal Impairment

    The influence of renal impairment on the pharmacokinetics of irinotecan has not been evaluated. Therefore, caution should be undertaken in patients with impaired renal function. Irinotecan is not recommended for use in patients on dialysis [see Use in Specific Populations (8.6)].

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  • 13 NONCLINICAL TOXICOLOGY

    13.1 Carcinogenesis, Mutagenesis, Impairment of Fertility

    Long-term carcinogenicity studies with irinotecan were not conducted. Rats were, however, administered intravenous doses of 2 mg/kg or 25 mg/kg irinotecan once per week for 13 weeks (in separate studies, the 25 mg/kg dose produced an irinotecan Cmax and AUC that were about 7.0 times and 1.3 times the respective values in patients administered 125 mg/m2 weekly) and were then allowed to recover for 91 weeks. Under these conditions, there was a significant linear trend with dose for the incidence of combined uterine horn endometrial stromal polyps and endometrial stromal sarcomas. Irinotecan was clastogenic both in vitro (chromosome aberrations in Chinese hamster ovary cells) and in vivo (micronucleus test in mice). Neither irinotecan nor its active metabolite SN-38 was mutagenic in the in vitro Ames assay.

    No significant adverse effects on fertility and general reproductive performance were observed after intravenous administration of irinotecan in doses of up to 6 mg/kg/day to rats and rabbits; however, atrophy of male reproductive organs was observed after multiple daily irinotecan doses both in rodents at 20 mg/kg and in dogs at 0.4 mg/kg. In separate studies in rodents, this dose produced an irinotecan Cmax and AUC about 5 and 1 times, respectively, of the corresponding values in patients administered 125 mg/m2 weekly. In dogs this dose produced an irinotecan Cmax and AUC about one-half and 1/15th, respectively, of the corresponding values in patients administered 125 mg/m2 weekly.

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  • 14 CLINICAL STUDIES

    Irinotecan has been studied in clinical trials in combination with 5-fluorouracil (5-FU) and leucovorin (LV) and as a single agent [see Dosage and Administration (2)]. When given as a component of combination-agent treatment, irinotecan was either given with a weekly schedule of bolus 5-FU/LV or with an every-2-week schedule of infusional 5-FU/LV. Weekly and once-every-3-week dosage schedules were used for the single-agent irinotecan studies. Clinical studies of combination and single-agent use are described below.

    14.1 Metastatic Colorectal Cancer

    First Line Therapy in Combination with 5-FU/LV: Studies 1 and 2

    Two phase 3, randomized, controlled, multinational clinical trials support the use of CAMPTOSAR Injection as first-line treatment of patients with metastatic carcinoma of the colon or rectum. In each study, combinations of irinotecan with 5-FU and LV were compared with 5-FU and LV alone. Study 1 compared combination irinotecan/bolus 5-FU/LV therapy given weekly with a standard bolus regimen of 5-FU/LV alone given daily for 5 days every 4 weeks; an irinotecan-alone treatment arm given on a weekly schedule was also included. Study 2 evaluated two different methods of administering infusional 5-FU/LV, with or without irinotecan. In both studies, concomitant medications such as antiemetics, atropine, and loperamide were given to patients for prophylaxis and/or management of symptoms from treatment. In Study 2, a 7-day course of fluoroquinolone antibiotic prophylaxis was given in patients whose diarrhea persisted for greater than 24 hours despite loperamide or if they developed a fever in addition to diarrhea. Treatment with oral fluoroquinolone was also initiated in patients who developed an absolute neutrophil count (ANC) <500/mm3, even in the absence of fever or diarrhea. Patients in both studies also received treatment with intravenous antibiotics if they had persistent diarrhea or fever or if ileus developed.

    In both studies, the combination of irinotecan/5-FU/LV therapy resulted in significant improvements in objective tumor response rates, time to tumor progression, and survival when compared with 5-FU/LV alone. These differences in survival were observed in spite of second-line therapy in a majority of patients on both arms, including crossover to irinotecan-containing regimens in the control arm. Patient characteristics and major efficacy results are shown in Table 10.

    Table 10. Combination Dosage Schedule: Study Results
    Study 1 Study 2
    Irinotecan + Bolus 5-FU/LV weekly × 4 every 6 weeks Bolus 5-FU/LV daily × 5 every 4 weeks Irinotecan weekly × 4 every 6 weeks Irinotecan + Infusional 5-FU/LV Infusional 5-FU/LV
    *
    Study 1: N=225 (irinotecan/5-FU/LV),N=219 (5-FU/LV),N=223 (irinotecan)
    Study 2: N=199 (irinotecan/5-FU/LV),N=186 (5-FU/LV)
    Confirmed ≥ 4 to 6 weeks after first evidence of objective response
    Chi-square test
    §
    Log-rank test
    Number of patients 231 226 226 198 187
    Demographics and treatment administration
    Female/Male (%) 34/65 45/54 35/64 33/67 47/53
    Median age in years (range) 62 (25–85) 61 (19–85) 61 (30–87) 62 (27–75) 59 (24–75)
    Performance status (%)
    0 39 41 46 51 51
    1 46 45 46 42 41
    2 15 13 8 7 8
    Primary tumor (%)
    Colon 81 85 84 55 65
    Rectum 17 14 15 45 35
    Median time from diagnosis to randomization (months, range) 1.9
    (0–161)
    1.7
    (0–203)
    1.8
    (0.1–185)
    4.5
    (0–88)
    2.7
    (0–104)
    Prior adjuvant 5-FU therapy (%)
    No
    Yes
    89
    11
    92
    8
    90
    10
    74
    26
    76
    24
    Median duration of study treatment* (months) 5.5 4.1 3.9 5.6 4.5
    Median Relative Dose Intensity (%)*
    Irinotecan
    5-FU
    72
    71

    86
    75
    87
    86

    93
    Efficacy Results
    Confirmed objective tumor response rate (%) 39 21 18 35 22
    (p<0.0001) (p<0.005)
    Median time to tumor progression§
    (months)
    7.0 4.3 4.2 6.7 4.4
    (p=0.004)§ (p<0.001)§
    Median survival
    (months)
    14.8 12.6 12.0 17.4 14.1
    (p<0.05)§ (p<0.05)§

    Improvement was noted with irinotecan-based combination therapy relative to 5-FU/LV when response rates and time to tumor progression were examined across the following demographic and disease-related subgroups (age, gender, ethnic origin, performance status, extent of organ involvement with cancer, time from diagnosis of cancer, prior adjuvant therapy, and baseline laboratory abnormalities). Figures 1 and 2 illustrate the Kaplan-Meier survival curves for the comparison of irinotecan/5-FU/LV versus 5-FU/LV in Studies 1 and 2, respectively.

    Figure 1
    Figure 2

    Second-Line Therapy After 5-FU-Based Treatment

    4 Weekly Doses on a 6-Week Cycle: Studies 3, 4, and 5

    Data from three open-label, single-agent, clinical studies, involving a total of 304 patients in 59 centers, support the use of CAMPTOSAR in the treatment of patients with metastatic cancer of the colon or rectum that has recurred or progressed following treatment with 5-FU-based therapy. These studies were designed to evaluate tumor response rate and do not provide information on effects on survival and disease-related symptoms. In each study, CAMPTOSAR was administered in repeated 6-week cycles consisting of a 90-minute intravenous infusion once weekly for 4 weeks, followed by a 2-week rest period. Starting doses of CAMPTOSAR in these trials were 100, 125, or 150 mg/m2, but the 150-mg/m2 dose was poorly tolerated (due to high rates of grade 4 late diarrhea and febrile neutropenia). Study 3 enrolled 48 patients and was conducted by a single investigator at several regional hospitals. Study 4 was a multicenter study conducted by the North Central Cancer Treatment Group. All 90 patients enrolled in Study 4 received a starting dose of 125 mg/m2. Study 5 was a multicenter study that enrolled 166 patients from 30 institutions. The initial dose in Study 5 was 125 mg/m2 but was reduced to 100 mg/m2 because the toxicity seen at the 125-mg/m2 dose was perceived to be greater than that seen in previous studies. All patients in these studies had metastatic colorectal cancer, and the majority had disease that recurred or progressed following a 5-FU-based regimen administered for metastatic disease. The results of the individual studies are shown in Table 11.

    Table 11. Weekly Dosage Schedule: Study Results
    Study
    3 4 5
    *
    Nine patients received 150 mg/m 2 as a starting dose; two (22.2%) responded to CAMPTOSAR.
    Relative dose intensity for CAMPTOSAR based on planned dose intensity of 100, 83.3, and 66.7 mg/m 2/wk corresponding with 150, 125, and 100 mg/m 2 starting doses, respectively.
    Confirmed ≥ 4 to 6 weeks after first evidence of objective response.
    Number of Patients 48 90 64 102
    Starting Dose (mg/m2/week × 4) 125* 125 125 100
    Demographics and Treatment Administration
    Female/Male (%) 46/54 36/64 50/50 51/49
    Median Age in years (range) 63 (29–78) 63 (32–81) 61 (42–84) 64 (25–84)
    Ethnic Origin (%)
      White 79 96 81 91
      African American 12 4 11 5
      Hispanic 8 0 8 2
      Oriental/Asian 0 0 0 2
    Performance Status (%)
      0 60 38 59 44
      1 38 48 33 51
      2 2 14 8 5
    Primary Tumor (%)
      Colon 100 71 89 87
      Rectum 0 29 11 8
      Unknown 0 0 0 5
    Prior 5-FU Therapy (%)
      For Metastatic Disease 81 66 73 68
      ≤ 6 months after Adjuvant 15 7 27 28
      > 6 months after Adjuvant 2 16 0 2
      Classification Unknown 2 12 0 3
    Prior Pelvic/Abdominal Irradiation (%)
      Yes 3 29 0 0
      Other 0 9 2 4
      None 97 62 98 96
    Duration of Treatment with CAMPTOSAR (median, months)
    5

    4

    4

    3
    Relative Dose Intensity (median %) 74 67 73 81
    Efficacy
    Confirmed Objective Response Rate (%)
    (95% CI)
    21
    (9.3 – 32.3)
    13
    (6.3 – 20.4)
    14
    (5.5 – 22.6)
    9
    (3.3 – 14.3)
    Time to Response (median, months) 2.6 1.5 2.8 2.8
    Response Duration (median, months) 6.4 5.9 5.6 6.4
    Survival (median, months) 10.4 8.1 10.7 9.3
    1-Year Survival (%) 46 31 45 43

    In the intent-to-treat analysis of the pooled data across all three studies, 193 of the 304 patients began therapy at the recommended starting dose of 125 mg/m2. Among these 193 patients, 2 complete and 27 partial responses were observed, for an overall response rate of 15.0% (95% Confidence Interval [CI], 10.0% to 20.1%) at this starting dose. A considerably lower response rate was seen with a starting dose of 100 mg/m2. The majority of responses were observed within the first two cycles of therapy, but responses did occur in later cycles of treatment (one response was observed after the eighth cycle). The median response duration for patients beginning therapy at 125 mg/m2 was 5.8 months (range, 2.6 to 15.1 months). Of the 304 patients treated in the three studies, response rates to CAMPTOSAR were similar in males and females and among patients older and younger than 65 years. Rates were also similar in patients with cancer of the colon or cancer of the rectum and in patients with single and multiple metastatic sites. The response rate was 18.5% in patients with a performance status of 0 and 8.2% in patients with a performance status of 1 or 2. Patients with a performance status of 3 or 4 have not been studied. Over half of the patients responding to CAMPTOSAR had not responded to prior 5-FU. Patients who had received previous irradiation to the pelvis responded to CAMPTOSAR at approximately the same rate as those who had not previously received irradiation.

    Once-Every-3-Week Dosage Schedule

    Single Arm Study: Study 6

    Data from an open-label, single-agent, single-arm, multicenter, clinical study involving a total of 132 patients support a once every-3-week dosage schedule of irinotecan in the treatment of patients with metastatic cancer of the colon or rectum that recurred or progressed following treatment with 5-FU. Patients received a starting dose of 350 mg/m2 given by 30-minute intravenous infusion once every 3 weeks. Among the 132 previously treated patients in this trial, the intent-to-treat response rate was 12.1% (95% CI, 7.0% to 18.1%).

    Randomized Studies: Studies 7 and 8

    Two multicenter, randomized, clinical studies further support the use of irinotecan given by the once-every-3-week dosage schedule in patients with metastatic colorectal cancer whose disease has recurred or progressed following prior 5-FU therapy. In Study 7, second-line irinotecan therapy plus best supportive care was compared with best supportive care alone. In Study 8, second-line irinotecan therapy was compared with infusional 5-FU-based therapy. In both studies, irinotecan was administered intravenously at a starting dose of 350 mg/m2 over 90 minutes once every 3 weeks. The starting dose was 300 mg/m2 for patients who were 70 years and older or who had a performance status of 2. The highest total dose permitted was 700 mg. Dose reductions and/or administration delays were permitted in the event of severe hematologic and/or nonhematologic toxicities while on treatment. Best supportive care was provided to patients in both arms of Study 7 and included antibiotics, analgesics, corticosteroids, transfusions, psychotherapy, or any other symptomatic therapy as clinically indicated. In both studies, concomitant medications such as antiemetics, atropine, and loperamide were given to patients for prophylaxis and/or management of symptoms from treatment. If late diarrhea persisted for greater than 24 hours despite loperamide, a 7-day course of fluoroquinolone antibiotic prophylaxis was given. Patients in the control arm of the Study 8 received one of the following 5-FU regimens: (1) LV, 200 mg/m2 IV over 2 hours; followed by 5-FU, 400 mg/m2 IV bolus; followed by 5-FU, 600 mg/m2 continuous IV infusion over 22 hours on days 1 and 2 every 2 weeks; (2) 5-FU, 250 to 300 mg/m2/day protracted continuous IV infusion until toxicity; (3) 5-FU, 2.6 to 3 g/m2 IV over 24 hours every week for 6 weeks with or without LV, 20 to 500 mg/m2/day every week IV for 6 weeks with 2-week rest between cycles. Patients were to be followed every 3 to 6 weeks for 1 year.

    A total of 535 patients were randomized in the two studies at 94 centers. The primary endpoint in both studies was survival. The studies demonstrated a significant overall survival advantage for irinotecan compared with best supportive care (p=0.0001) and infusional 5-FU-based therapy (p=0.035) as shown in Figures 3 and 4. In Study 7, median survival for patients treated with irinotecan was 9.2 months compared with 6.5 months for patients receiving best supportive care. In Study 8, median survival for patients treated with irinotecan was 10.8 months compared with 8.5 months for patients receiving infusional 5-FU-based therapy. Multiple regression analyses determined that patients' baseline characteristics also had a significant effect on survival. When adjusted for performance status and other baseline prognostic factors, survival among patients treated with irinotecan remained significantly longer than in the control populations (p=0.001 for Study 7 and p=0.017 for Study 8). Measurements of pain, performance status, and weight loss were collected prospectively in the two studies; however, the plan for the analysis of these data was defined retrospectively. When comparing irinotecan with best supportive care in Study 7, this analysis showed a statistically significant advantage for irinotecan, with longer time to development of pain (6.9 months versus 2.0 months), time to performance status deterioration (5.7 months versus 3.3 months), and time to > 5% weight loss (6.4 months versus 4.2 months). Additionally, 33.3% (33/99) of patients with a baseline performance status of 1 or 2 showed an improvement in performance status when treated with irinotecan versus 11.3% (7/62) of patients receiving best supportive care (p=0.002). Because of the inclusion of patients with non-measurable disease, intent-to-treat response rates could not be assessed.

    Figure 3. Survival
    Second-Line Irinotecan vs Best Supportive Care (BSC)
    Study 7
    Figure 3
    Figure 4. Survival
    Second-Line Irinotecan vs Infusion 5-FU
    Study 8
    Figure 4
    Table 12. Once-Every-3-Week Dosage Schedule: Study Results
    Study 7 Study 8
    Irinotecan BSC* Irinotecan 5-FU
    *
    BSC = best supportive care
    Relative dose intensity for irinotecan based on planned dose intensity of 116.7 and 100 mg/m 2/wk corresponding with 350 and 300 mg/m 2 starting doses, respectively.
    Number of patients 189 90 127 129
    Demographics and treatment administration
    Female/Male (%) 32/68 42/58 43/57 35/65
    Median age in years (range) 59 (22–75) 62 (34–75) 58 (30–75) 58 (25–75)
    Performance status (%)
      0 47 31 58 54
      1 39 46 35 43
      2 14 23 8 3
    Primary tumor (%)
      Colon 55 52 57 62
      Rectum 45 48 43 38
    Prior 5-FU therapy (%)
      For metastatic disease 70 63 58 68
      As adjuvant treatment 30 37 42 32
    Prior irradiation (%) 26 27 18 20
    Duration of study treatment (median, months)
    (Log-rank test)
    4.1 -- 4.2
    (p=0.02)
    2.8
    Relative dose intensity (median %) 94 -- 95 81–99
      Survival
    Survival (median, months)
    (Log-rank test)
    9.2
    (p=0.0001)
    6.5 10.8
    (p=0.035)
    8.5

    In the two randomized studies, the EORTC QLQ-C30 instrument was utilized. At the start of each cycle of therapy, patients completed a questionnaire consisting of 30 questions, such as "Did pain interfere with daily activities?" (1 = Not at All, to 4 = Very Much) and "Do you have any trouble taking a long walk?" (Yes or No). The answers from the 30 questions were converted into 15 subscales, that were scored from 0 to 100, and the global health status subscale that was derived from two questions about the patient's sense of general well being in the past week. The results as summarized in Table 13 are based on patients' worst post-baseline scores. In Study 7, a multivariate analysis and univariate analyses of the individual subscales were performed and corrected for multivariate testing. Patients receiving irinotecan reported significantly better results for the global health status, on two of five functional subscales, and on four of nine symptom subscales. As expected, patients receiving irinotecan noted significantly more diarrhea than those receiving best supportive care. In Study 8, the multivariate analysis on all 15 subscales did not indicate a statistically significant difference between irinotecan and infusional 5-FU.

    Table 13. EORTC QLQ-C30: Mean Worst Post-Baseline Score*
    QLQ-C30 Subscale Study 7 Study 8
    Irinotecan BSC p-value Irinotecan 5-FU p-value
    *
    For the five functional subscales and global health status subscale, higher scores imply better functioning, whereas, on the nine symptom subscales, higher scores imply more severe symptoms. The subscale scores of each patient were collected at each visit until the patient dropped out of the study.
    Global health status 47 37 0.03 53 52 0.9
    Functional scales
    Cognitive 77 68 0.07 79 83 0.9
    Emotional 68 64 0.4 64 68 0.9
    Social 58 47 0.06 65 67 0.9
    Physical 60 40 0.0003 66 66 0.9
    Role 53 35 0.02 54 57 0.9
    Symptom Scales
    Fatigue 51 63 0.03 47 46 0.9
    Appetite loss 37 57 0.0007 35 38 0.9
    Pain assessment 41 56 0.009 38 34 0.9
    Insomnia 39 47 0.3 39 33 0.9
    Constipation 28 41 0.03 25 19 0.9
    Dyspnea 31 40 0.2 25 24 0.9
    Nausea/Vomiting 27 29 0.5 25 16 0.09
    Financial impact 22 26 0.5 24 15 0.3
    Diarrhea 32 19 0.01 32 22 0.2
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  • 15 REFERENCES

    • NIOSH Alert: Preventing occupational exposures to antineoplastic and other hazardous drugs in healthcare settings. 2004. U.S. Department of Health and Human Services, Public Health Service, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health, DHHS (NIOSH) Publication No. 2004-165.
    • OSHA Technical Manual, TED 1-0.15A, Section VI: Chapter 2. Controlling Occupational Exposure to Hazardous Drugs. OSHA, 1999. http://www.osha.gov/dts/osta/otm/otm_vi/otm_vi_2.html
    • American Society of Health-System Pharmacists. ASHP guidelines on handling hazardous drugs. Am J Health-Syst Pharm. 2006; 63:1172–1193.
    • Polovich, M., White, J. M., & Kelleher, L.O. (eds.) 2005. Chemotherapy and biotherapy guidelines and recommendations for practice (2nd. ed.) Pittsburgh, PA: Oncology Nursing Society.
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  • 16 HOW SUPPLIED/STORAGE AND HANDLING

    CAMPTOSAR Injection is available in single-dose brown glass vials in the following package sizes:

    2 mL NDC 0009-7529-02
    5 mL NDC 0009-7529-01

    CAMPTOSAR Injection is available in single-dose amber colored polypropylene CYTOSAFE® vials in the following package sizes:

    2 mL NDC 0009-7529-04
    5 mL NDC 0009-7529-03
    15 mL NDC 0009-7529-05

    Store at controlled room temperature 15° to 30°C (59° to 86°F). Protect from light. Keep the vial in the carton until the time of use.

    Inspect the vial for damage and visible signs of leaks before removing from the carton. If damaged, incinerate the unopened package.

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  • 17 PATIENT COUNSELING INFORMATION

    • Patients and caregivers should be informed of gastrointestinal complications, such as nausea, vomiting, abdominal cramping, and diarrhea. Patients should have loperamide readily available to begin treatment for late diarrhea (generally occurring more than 24 hours after administration of CAMPTOSAR). Begin loperamide at the first episode of poorly formed or loose stools or the earliest onset of bowel movements more frequent than normal. One dosage regimen for loperamide is 4 mg at the first onset of late diarrhea and then 2 mg every 2 hours until the patient is diarrhea-free for at least 12 hours. Loperamide is not recommended to be used for more than 48 consecutive hours at these doses, because of the risk of paralytic ileus. During the night, the patient may take 4 mg of loperamide every 4 hours. Patients should contact their physician if any of the following occur: diarrhea for the first time during treatment; black or bloody stools; symptoms of dehydration such as lightheadedness, dizziness, or faintness; inability to take fluids by mouth due to nausea or vomiting; or inability to get diarrhea under control within 24 hours.
    • Patients should be warned about the potential for dizziness or visual disturbances which may occur within 24 hours following the administration of CAMPTOSAR.
    • Explain the significance of routine blood cell counts. Instruct patients to monitor their temperature frequently and immediately report any occurrence of fever or infection.
    • CAMPTOSAR may cause fetal harm. Advise patients to avoid becoming pregnant while receiving this drug.
    • Patients should be alerted to the possibility of alopecia.
    • Contains sorbitol.
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  • SPL UNCLASSIFIED SECTION

    This product's label may have been updated. For current full prescribing information, please visit www.pfizer.com.

    Logo

    Licensed from Yakult Honsha Co., LTD, Japan, and Daiichi Pharmaceutical Co., LTD, Japan

    LAB-0134-18.0

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  • PRINCIPAL DISPLAY PANEL

    PRINCIPAL DISPLAY PANEL - 100 mg/5 mL Vial Label

    NDC 0009-7529-03
    Single Use: Discard unused portion

    Camptosar®
    irinotecan HCl injection

    100 mg/5 mL
    (20 mg/mL)

    For Intravenous Use Only
    Cytosafe® Vial
    Caution: Cytotoxic Agent

    PRINCIPAL DISPLAY PANEL - 100 mg/5 mL Vial Label
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  • PRINCIPAL DISPLAY PANEL

    PRINCIPAL DISPLAY PANEL - 100 mg/5 mL Vial Carton

    NDC 0009-7529-03
    Rx only

    Single Use: Discard unused portion
    Camptosar®

    irinotecan hydrochloride
    injection

    100 mg/5 mL
    (20 mg/mL)

    For Intravenous Use Only

    Cytosafe® Vial
    Caution: Cytotoxic Agent

    Pfizer Injectables

    PRINCIPAL DISPLAY PANEL - 100 mg/5 mL Vial Carton
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  • INGREDIENTS AND APPEARANCE
    CAMPTOSAR 
    irinotecan hydrochloride injection, solution
    Product Information
    Product Type HUMAN PRESCRIPTION DRUG LABEL Item Code (Source) NDC:0009-7529
    Route of Administration INTRAVENOUS DEA Schedule     
    Active Ingredient/Active Moiety
    Ingredient Name Basis of Strength Strength
    IRINOTECAN HYDROCHLORIDE (IRINOTECAN) IRINOTECAN HYDROCHLORIDE 20 mg  in 1 mL
    Inactive Ingredients
    Ingredient Name Strength
    LACTIC ACID  
    SODIUM HYDROXIDE  
    HYDROCHLORIC ACID  
    Packaging
    # Item Code Package Description Marketing Start Date Marketing End Date
    1 NDC:0009-7529-02 1 in 1 CARTON
    1 2 mL in 1 VIAL, SINGLE-DOSE
    2 NDC:0009-7529-01 1 in 1 CARTON
    2 5 mL in 1 VIAL, SINGLE-DOSE
    3 NDC:0009-7529-04 1 in 1 CARTON
    3 2 mL in 1 VIAL, SINGLE-DOSE
    4 NDC:0009-7529-03 1 in 1 CARTON
    4 5 mL in 1 VIAL, SINGLE-DOSE
    5 NDC:0009-7529-05 1 in 1 CARTON
    5 15 mL in 1 VIAL, SINGLE-DOSE
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    NDA NDA020571 06/14/1996
    Labeler - Pharmacia and Upjohn Company (829076566)
    Establishment
    Name Address ID/FEI Business Operations
    Pfizer Ireland Pharmaceuticals 989811526 MANUFACTURE(0009-7529)
    Establishment
    Name Address ID/FEI Business Operations
    Pfizer Cork Limited 988786778 MANUFACTURE(0009-7529)
    Establishment
    Name Address ID/FEI Business Operations
    Fresenius Kabi Oncology Limited 915786944 API MANUFACTURE(0009-7529)
    Establishment
    Name Address ID/FEI Business Operations
    Yakult Honsha Co. Ltd. 706252103 API MANUFACTURE(0009-7529)
    Establishment
    Name Address ID/FEI Business Operations
    Pfizer (Perth) Pty Limited 757868963 API MANUFACTURE(0009-7529), MANUFACTURE(0009-7529)
    Establishment
    Name Address ID/FEI Business Operations
    Pharmacia and Upjohn Company 829076566 MANUFACTURE(0009-7529)
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