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COMPLETED
NCT00953537
NA

Predicting Response to Capecitabine in Women With Metastatic Breast Cancer

Sponsor: Centre Antoine Lacassagne

View on ClinicalTrials.gov

Summary

RATIONALE: Identifying genes that increase a person's susceptibility to side effects caused by capecitabine may help doctors plan better treatment. PURPOSE: This clinical trial is studying blood samples in predicting response to capecitabine in women with metastatic breast cancer.

Official title: Multicentric Pilot Study of Dihydropyrimidine Dehydrogenase (DPD) Deficiency for Predicting Capecitabine Toxicity in Breast Cancer Patients

Key Details

Gender

FEMALE

Age Range

18 Years - 120 Years

Study Type

INTERVENTIONAL

Enrollment

303

Start Date

2009-01

Completion Date

2011-02

Last Updated

2026-05-05

Healthy Volunteers

No

Conditions

Interventions

DRUG

capecitabine

OTHER

laboratory biomarker analysis

OTHER

pharmacological study

Locations (1)

Centre Antoine Lacassagne

Nice, France