Study of Glutamine as Prophylaxis for Irinotecan Induced Diarrhea

Last updated: February 24, 2016
Sponsor: AHS Cancer Control Alberta
Overall Status: Completed

Phase

2

Condition

Metastatic Cancer

Lactose Intolerance

Colorectal Cancer

Treatment

N/A

Clinical Study ID

NCT00255229
GI-05-0024
  • Ages > 18
  • All Genders

Study Summary

Irinotecan (7-ethyl-10- {4(-1-piperidino)-1-piperidino} carbonyloxy camptothecin) is a semisynthetic camptothecin derivative introduced in the 1980's. Irinotecan is a prodrug metabolized by carboxylesterases to an active metabolite 7-ethyl-10-hydroxy-camptothecin (SN38). SN38 exerts its cytotoxic effect by forming stable complexes with topoisomerase I and DNA. These complexes collide with replication forks and cause breaks in DNA. Studies substantiated irinotecan's activity in 5FU resistant colorectal cancer and led to its approval for treatment of 5FU resistant colorectal cancer in the United States, Canada and Europe.Colorectal cancer studies demonstrated that single agent irinotecan's dose limiting toxicity was diarrhea occurring 5 to 6 days after its administration. High dose loperamide at first occurrence of diarrhea has decreased the incidence of diarrhea but the incidence of grade 3/4 diarrhea remains high at 28 to 40%.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • metastatic colorectal cancer to be treated with FOLFIAT chemo

Exclusion

Exclusion Criteria:

  • severely abnormal liver and kidney function

Study Design

Total Participants: 130
Study Start date:
December 01, 2002
Estimated Completion Date:
January 31, 2010

Connect with a study center

  • Cross Cancer Institute

    Edmonton, Alberta T6G 1Z2
    Canada

    Site Not Available

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