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Clinical Trials/NCT00870168
NCT00870168
Completed
Not Applicable

Modifications of Hormone Receptors and Biological Parameters of Metastatic Breast Cancer Treated With First-line Chemotherapy. Prospective Biological Study.

Centre Jean Perrin1 site in 1 country60 target enrollmentJanuary 2006

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Breast Cancer
Sponsor
Centre Jean Perrin
Enrollment
60
Locations
1
Primary Endpoint
Changes in hormone receptor expression
Status
Completed
Last Updated
14 years ago

Overview

Brief Summary

RATIONALE: Studying biopsy samples in the laboratory from patients with cancer may help doctors learn more about changes that occur in DNA and identify biomarkers related to cancer.

PURPOSE: This clinical trial is studying biopsy samples in women who are receiving first-line chemotherapy for metastatic breast cancer.

Detailed Description

OBJECTIVES: Primary * Evaluate the effect of first-line chemotherapy on expression of hormone receptors and biomarkers in women with metastatic breast cancer. Secondary * Assess changes in HER1 and HER2 expression during treatment. OUTLINE: This is a multicenter study. Patients receive 6-9 courses of front-line chemotherapy according to the investigator. Patients with estrogen receptor- and/or progesterone receptor-positive disease receive hormone therapy. Patients undergo biopsy prior to and after completion of chemotherapy for examination of hormone receptors and HER1 and HER2 expression. After completion of study treatment, patients are followed every 6 months for 5 years.

Registry
clinicaltrials.gov
Start Date
January 2006
End Date
May 2011
Last Updated
14 years ago
Study Type
Interventional
Sex
Female

Investigators

Sponsor
Centre Jean Perrin

Eligibility Criteria

Inclusion Criteria

  • Not provided

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Changes in hormone receptor expression

Study Sites (1)

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