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Clinical Trials/NCT00896623
NCT00896623
Completed
Not Applicable

Pharmacogenetics in Relation to Breast Cancer Outcomes in SWOG 8897

SWOG Cancer Research Network0 sites1,577 target enrollmentDecember 2006
ConditionsBreast Cancer

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
SWOG Cancer Research Network
Enrollment
1577
Primary Endpoint
Differences in outcome according to common variant alleles
Status
Completed
Last Updated
9 years ago

Overview

Brief Summary

RATIONALE: Studying samples of tissue from patients with cancer in the laboratory may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer. It may also help doctors predict a patient's response to treatment.

PURPOSE: This laboratory study is looking at DNA in tissue samples from women with breast cancer to see if it can predict treatment outcome.

Detailed Description

OBJECTIVES: * Determine if polymorphisms resulting in greater activation of cyclophosphamide (CYP2B6, CYP3A4, and CYP3A5) are associated with disease-free survival and treatment toxicities in women with breast cancer. * Determine if polymorphisms resulting in less production of quinone-related oxidative damage of doxorubicin hydrochloride (NQO1, NQO2, NOS2, NOS3, CBR3) are associated with disease-free survival and treatment toxicities in these patients. OUTLINE: This is a multicenter study. Tissue samples archived on clinical trial SWOG-8897 are genotyped for polymorphisms in the CYP3A4, CYP3A5, CYP2B6, NQO1, NQO2, NOS2, NOS3, and CBR3 genes by matrix-assisted laser desorption ionization-time-of-flight mass spectrometry. Variant alleles are correlated with patient outcome. PROJECTED ACCRUAL: A total of 1,577 patients will be accrued for this study.

Registry
clinicaltrials.gov
Start Date
December 2006
End Date
June 2007
Last Updated
9 years ago
Study Type
Observational
Sex
Female

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Differences in outcome according to common variant alleles

Time Frame: Through study follow-up an average of 10.8 years

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