Study of Etoposide in Breast Cancer Patients

Sponsor
National Cancer Institute (NCI) (NIH)
Overall Status
Completed
CT.gov ID
NCT00026949
Collaborator
(none)
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Study Details

Study Description

Brief Summary

This study will examine how the body handles etoposide, a drug used to treat breast cancer. The knowledge gained may lead to more effective use of the drug with fewer side effects in the future.

Breast cancer patients who are receiving etoposide as part of their treatment may participate in this study. Patients will have 18 blood samples (about a teaspoon or less each) drawn over a 72-hour period during and after their infusion of etoposide. The initial blood samples cannot be taken from the same intravenous line (small tube placed in a vein) used to deliver the etoposide, so a second line may have to be placed temporarily to obtain these samples.

Condition or Disease Intervention/Treatment Phase

    Detailed Description

    Etoposide is a topoisomerase II inhibitor that has a broad range of anticancer activity at conventional doses (100 mg/m(2) daily x 5 days) and is administered in high doses (greater than 1200 mg/m(2)) as a component of pre-transplant myeloablative chemotherapy regimens. Etoposide pharmacokinetics are linear over a 30-fold dose range, but disposition is highly variable. Etoposide is highly protein bound (95%) to albumin, but protein binding (and therefore free drug concentrations) vary widely in cancer patients. Etoposide is eliminated by metabolism and renal excretion, which may also contribute to the variability. The pharmacokinetics of etoposide will be studied in patients receiving high-dose etoposide as part of their pre-transplant preparative regimen, and pharmacokinetic parameters generated from pharmacokinetic modeling will be correlated with clinical and laboratory characteristics and toxicity in order to develop more rational dosing methods.

    Study Design

    Study Type:
    Observational
    Official Title:
    Pharmacokinetics of Etoposide in Patients With Breast Cancer Receiving High-Dose Etoposide
    Study Start Date :
    Aug 1, 1999
    Study Completion Date :
    Aug 1, 2004

    Outcome Measures

    Primary Outcome Measures

      Eligibility Criteria

      Criteria

      Ages Eligible for Study:
      N/A and Older
      Sexes Eligible for Study:
      Female
      Accepts Healthy Volunteers:
      No

      INCLUSION CRITERIA

      Age greater than or equal to 18 years.

      Patients with breast cancer who are entered on existing Medicine Branch protocols that include high-dose etoposide.

      Must be able to provide informed consent.

      Contacts and Locations

      Locations

      Site City State Country Postal Code
      1 National Cancer Institute (NCI) Bethesda Maryland United States 20892

      Sponsors and Collaborators

      • National Cancer Institute (NCI)

      Investigators

      None specified.

      Study Documents (Full-Text)

      None provided.

      More Information

      Publications

      Responsible Party:
      , ,
      ClinicalTrials.gov Identifier:
      NCT00026949
      Other Study ID Numbers:
      • 990161
      • 99-C-0161
      First Posted:
      Nov 15, 2001
      Last Update Posted:
      Mar 4, 2008
      Last Verified:
      Aug 1, 2004
      Keywords provided by , ,
      Additional relevant MeSH terms:

      Study Results

      No Results Posted as of Mar 4, 2008