Gene Expression Profiles of Breast Cancer Treated With Sequential Adriamycin and Docetaxel in Relation to Tumor Responses
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- Metastatic Breast Cancer
- Sponsor
- National University Hospital, Singapore
- Enrollment
- 100
- Locations
- 1
- Primary Endpoint
- 1. Evaluate the impact of adriamycin and docetaxel on tumor gene expression profiles.
- Status
- Completed
- Last Updated
- 17 years ago
Overview
Brief Summary
We hypothesize that changes in tumor gene expression profiles vary in response to different sequences and types of chemotherapy, and that gene expression changes will correlate with tumor response. We are also looking to correlate drug pharmacokinetics and treatment toxicity with genotype of drug metabolizing enzymes and tranporters.Patients with metastatic breast cancer and who have measurable primary breast tumor will be randomized to one of two alternating sequences of adriamycin and docetaxel. Serial tumor biopsies and plasma samples will be obtained for gene expression and proteomic studies to identify biomarkers that will predict for chemotherapy response.
Detailed Description
Significant inter-individual variation exists in tumor response and chemotherapy toxicity because of unique tumor and patient factors. Individual drugs with distinct mechanisms of action may induce specific genomic and proteomic changes that may be used as predictor for response. We plan to study serial genomic and proteomic profiles in primary breast tumor treated with one of two sequences of alternating adriamycin (A) and docetaxel (T), A\>T\>A\>T\>A\>T, or T\>A\>T\>A\>T\>A, at 75mg/m2 3 weekly for each drug. Pharmacokinetic analysis of both drugs will be performed; amplified tumor RNA will be hybridized on Affymetrix® HG-U133+2 array; tumor proteins will be fractionated and profiled with ProteinChip® Array SELDI MS (Ciphergen). Tumor gene expression and proteomic changes will be correlated with treatment response to identify biomarkers that may predict chemotherapy sensitivity.
Investigators
Eligibility Criteria
Inclusion Criteria
- •Female, age \> 18 years.
- •Histologic or cytologic diagnosis of breast carcinoma.
- •Stage II to IV breast cancer with measurable primary breast tumor, defined as palpable tumor with both diameters 2.0cm or greater as measured by caliper.
- •Patients must not have received prior chemotherapy or hormonal therapy for the treatment of breast cancer.
- •Karnofsky performance status of 70 or higher.
- •Estimated life expectancy of at least 12 weeks.
- •Adequate organ function including the following:
- •Bone marrow: White blood cells (WBC) \>= 3.5 x 109/L Absolute neutrophil (segmented and bands) count (ANC) \>= 1.5 x 109/L Platelets \>= 100 x 109/L Haemoglobin \>= 9g/dL
- •Hepatic: Bilirubin \<= 1.5 x upper limit of normal (ULN), ALT or AST \<= 2.5x ULN, (or \<=5 X with liver metastases) Alkaline phosphatase \<= 2.5x ULN.
- •Renal: creatinine \<= 1.5x ULN
Exclusion Criteria
- •Prior treatment for locally advanced or metastatic breast cancer.
- •Treatment within the last 30 days with any investigational drug.
- •Concurrent administration of any other tumor therapy, including cytotoxic chemotherapy, hormonal therapy, and immunotherapy.
- •Active infection that in the opinion of the investigator would compromise the patient's ability to tolerate therapy.
- •Pregnancy.
- •Breast feeding.
- •Serious concomitant disorders that would compromise the safety of the patient or compromise the patient's ability to complete the study, at the discretion of the investigator.
- •Poorly controlled diabetes mellitus.
- •Second primary malignancy that is clinically detectable at the time of consideration for study enrollment.
- •Symptomatic brain metastasis.
Outcomes
Primary Outcomes
1. Evaluate the impact of adriamycin and docetaxel on tumor gene expression profiles.
2. Correlate overall tumor response with tumor gene expression profiles.
Secondary Outcomes
- To correlate adriamycin and docetaxel pharmacokinetics with:
- 1. Genetic polymorphisms of MDR-1, Cyp3A and GSTs.
- 2. Drug toxicity and tumor response.