Overview

Evaluation of Drug Resistance in Patients With Metastatic Breast Cancer

Status:
Unknown status
Trial end date:
1969-12-31
Target enrollment:
0
Participant gender:
All
Summary
RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Some patients may develop a resistance to chemotherapy drugs. PURPOSE: Phase II trial to determine the reliability of a test for measuring drug resistance to paclitaxel in patients with metastatic breast cancer.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Oncotech
Treatments:
Albumin-Bound Paclitaxel
Antineoplastic Agents
Paclitaxel
Criteria
DISEASE CHARACTERISTICS: Metastatic breast cancer that is accessible for biopsy or
aspiration Bidimensionally measurable disease with at least one diameter greater than 1 cm
documented on x-ray or photograph, or a palpable lesion No brain metastases or
carcinomatous meningitis Hormone receptor status: Not specified

PATIENT CHARACTERISTICS: Age: 18 and over Sex: Male or female Menopausal status: Not
specified Performance status: SWOG 0-2 Life expectancy: Not specified Hematopoietic:
Absolute neutrophil count greater than 1,500/mm3 Platelet count greater than 100,000/mm3
Hepatic: Bilirubin no greater than 2.0 mg/dL SGOT no greater than 3 times upper limit of
normal (ULN) (no greater than 5 times ULN if metastatic to liver) Renal: Creatinine no
greater than 2.0 mg/dL Calcium no greater than 12 mg/dL Cardiovascular: No myocardial
infarction within 3 months prior to study No unstable angina or symptomatic congestive
heart failure Other: No active or uncontrolled infection Not HIV positive No psychoses Not
pregnant or nursing Effective contraception required of fertile women No second malignancy
within past 5 years except: Adequately treated basal or squamous cell carcinoma of the skin
In situ cancer of the cervix

PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: See Disease
Characteristics Prior paclitaxel permitted if patient had disease-free interval of greater
than 1 year Prior taxotere permitted Endocrine therapy: Not specified Radiotherapy: Not
specified Surgery: Not specified