Expired Study
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New York, New York 10032


Purpose:

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 combining docetaxel and carboplatin in treating patients who have stage III or stage IV ovarian cancer, fallopian tube cancer, or primary peritoneal cancer.


Study summary:

OBJECTIVES: - Evaluate the response rate, duration of response, and progression-free and overall survival of previously untreated patients with suboptimally debulked stage III or stage IV ovarian carcinoma, fallopian tube carcinoma, papillary serous cancer of the uterus, or primary peritoneal carcinoma treated with docetaxel and carboplatin. - Evaluate the feasibility and toxicity of this regimen in these patients. - Evaluate the effect of this regimen on quality of life of these patients. OUTLINE: This is an open-label study. Patients receive docetaxel IV over 1 hour and carboplatin IV over 30 minutes on day 1. Treatment repeats every 21 days for up to 6 courses in the absence of disease progression or unacceptable toxicity. Quality of life is assessed prior to therapy and then after every 3 courses of chemotherapy. PROJECTED ACCRUAL: Approximately 14-40 patients will be accrued for this study within 2.5 years.


Criteria:

DISEASE CHARACTERISTICS: - Histologically confirmed previously untreated ovarian cancer, fallopian tube carcinoma, papillary serous cancer of the uterus, or primary peritoneal carcinoma - Suboptimally debulked stage III or suboptimally or optimally debulked stage IV - Measurable or evaluable disease - CNS lesions, lytic bone lesions, and radiated lesions (unless there is documented progression after radiotherapy) are not considered measurable - CA 125 levels above 49 units/mL in the absence of cirrhosis or nonmalignant gross ascites are considered evaluable - Ineligible for other high-priority national or institutional study PATIENT CHARACTERISTICS: Age: - Over 18 Performance status: - ECOG 0-1 Life expectancy: - More than 2 months Hematopoietic: - WBC greater than 3,000/mm3 - Platelet count greater than 100,000/mm3 Hepatic: - Bilirubin less than 1.5 times upper limit of normal (ULN) - SGOT and/or SGPT less than 2.5 times ULN OR - SGOT and/or SGPT no greater than 2.5 times ULN if alkaline phosphatase no greater than ULN OR - Alkaline phosphatase no greater than 4 times ULN if SGOT and/or SGPT no greater than ULN - No SGOT and/or SGPT greater than 1.5 times ULN with alkaline phosphatase greater than 2.5 times ULN - Alkaline phosphatase less than 350 U/L Renal: - BUN less than 1.5 times normal - Creatinine less than 1.5 times ULN Other: - No other malignancy within the past 5 years except curatively treated carcinoma in situ of the cervix or skin cancer - No other serious medical or psychiatric illness - Not pregnant or nursing - Fertile patients must use effective contraception PRIOR CONCURRENT THERAPY: Biologic therapy: - Not specified Chemotherapy: - No prior chemotherapy - No other concurrent chemotherapy Endocrine therapy: - No concurrent hormone therapy Radiotherapy: - See Disease Characteristics - No prior radiotherapy Surgery: - See Disease Characteristics


NCT ID:

NCT00003560


Primary Contact:

Study Chair
Amy D. Tiersten, MD
Herbert Irving Comprehensive Cancer Center


Backup Contact:

N/A


Location Contact:

New York, New York 10032
United States



There is no listed contact information for this specific location.

Site Status: N/A


Data Source: ClinicalTrials.gov

Date Processed: September 19, 2017

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