A Pilot Study to Establish a Standardized Protocol for Gene Microarray Analysis in Patients Receiving Neoadjuvant Chemotherapy for Breast Cancer: Identifying Factors Predictive of a Response to Paclitaxel
- Determine the feasibility of accruing women with unresected infiltrating carcinoma of
the breast to a clinical trial involving serial breast biopsies and administration of
neoadjuvant paclitaxel before formal assessment of axillary lymph node status.
- Determine a standard protocol template for gene microarray analysis, in terms of the
timing and method of collecting tissue samples, before and after administration of
neoadjuvant paclitaxel in these patients.
- Determine the safety and efficacy of tissue sampling in these patients.
- Identify gene(s) or gene clusters that exhibit significant differences between
responding and non-responding tumors before treatment with neoadjuvant paclitaxel in
- Identify gene(s) or gene clusters that exhibit changes in gene expression before and
after the administration of neoadjuvant paclitaxel in these patients.
- Compare significant differences in gene expression between responding and
non-responding tumors in patients treated with this drug.
- Develop, preliminarily, a statistical model utilizing individual genes and/or gene
clusters that can best predict response to paclitaxel in these patients.
OUTLINE: This is a pilot, multicenter study.
Patients undergo core needle breast biopsy within 14 days before starting neoadjuvant
paclitaxel treatment. Patients receive neoadjuvant paclitaxel IV over 3 hours on day 1.
Treatment repeats every 21 days for up to 4 courses in the absence of disease progression or
Patients undergo core needle breast biopsy 48 hours after the first administration of
paclitaxel, upon completion of course 1, and either upon completion of the last course (in
patients with clinical or radiographic evidence of residual disease) or during definitive
breast surgery. Biopsy samples are analyzed for gene expression by gene microarray analysis.
Patients are followed for survival.
PROJECTED ACCRUAL: A total of 40 patients will be accrued for this study within 2 years.
Endpoint Classification: Pharmacodynamics Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Diagnostic
Minetta C. Liu, MD
Lombardi Cancer Research Center
United States: Food and Drug Administration
|Lombardi Comprehensive Cancer Center at Georgetown University Medical Center||Washington, District of Columbia 20007|