Overview
Docetaxel Combined With Estramustine in Treating Women With Metastatic Breast Cancer
Status:
Unknown status
Unknown status
Trial end date:
1969-12-31
1969-12-31
Target enrollment:
0
0
Participant gender:
Female
Female
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Combining more than one drug may kill more tumor cells. PURPOSE: Phase II trial to study the effectiveness of docetaxel combined with estramustine in treating women with metastatic breast cancer.Phase:
Phase 2Accepts Healthy Volunteers?
NoDetails
Lead Sponsor:
Herbert Irving Comprehensive Cancer CenterTreatments:
Docetaxel
Estramustine
Criteria
DISEASE CHARACTERISTICS: Histologically confirmed metastatic breast cancer Measurable orevaluable disease Must be ineligible for other high priority national or institutional
study No visible metastases on brain CT or MRI (unless single lesion amenable to surgical
resection) Hormone receptor status: Not specified
PATIENT CHARACTERISTICS: Age: Over 18 Sex: Female Menopausal status: Not specified
Performance status: ECOG 0-2 Life expectancy: More than 2 months Hematopoietic: WBC greater
than 3,000/mm3 Platelet count greater than 100,000/mm3 No prior clotting disorder unless
therapeutically anticoagulated Hepatic: Bilirubin less than the upper limit of normal SGOT
or SGPT less than 1.5 times normal Renal: BUN less than 1.5 times normal Creatinine less
than 1.5 times normal Cardiovascular: No prior thromboembolism unless therapeutically
anticoagulated Other: No symptomatic ascites, pleural effusion or peripheral edema No
serious medical or psychiatric illness No prior malignancy other than curatively treated
carcinoma in situ of the cervix or skin cancer
PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: At least 4 weeks
since prior chemotherapy (2 weeks if weekly regimen) Any number of prior chemotherapy
regimens allowed Endocrine therapy: Any number of prior hormonal therapy regimens allowed
Radiotherapy: At least 4 weeks since prior radiotherapy Surgery: At least 1 week since
prior surgery