Gemcitabine Plus Carboplatin Versus Carboplatin Monotherapy in Patients With Advanced Ovarian Cancer

Phase 3

Completed

• Conditions: Ovarian Cancer

• Registration Number: NCT00102414
• Lead Sponsor: AGO Study Group

Brief Summary

The primary objective of this study is to compare the time to progressive disease in patients treated with gemcitabine plus carboplatin versus carboplatin monotherapy. Patients will have advanced epithelial ovarian cancer and have failed first-line platinum-containing therapy 6 months after treatment discontinuation.

Detailed Description

Carboplatin is commonly used for the treatment of ovarian cancer in first- and second-line therapy. The efficacy of gemcitabine in ovarian carcinoma was researched in various Phase 2 studies.

Study Timeline

• Study Start: 1999-09
• Study Completion: 2004-11
• Status Verified: 2005-01
• Study First Submitted QC: 2005-01-28
• Study First Submitted: 2005-01-29
• Study First Posted: 2005-01-31
• Last Update Submitted: 2006-11-13
• Last Update Posted: 2006-11-14

Recruitment & Eligibility

• Status: COMPLETED
• Sex: Female
• Target Recruitment: 356

Inclusion Criteria

• Histologically proven ovarian cancer with evidence of recurrence or progression
• Failed first-line platinum containing therapy after 6 months of treatment discontinuation
• Documented lesion as evidenced by appropriate computerized tomography (CT), magnetic resonance imaging (MRI) scan, chest x-ray, or ultrasound.
• Previous hormonal therapy or radiotherapy must be terminated at least 3 weeks before study drug administration
• Adequate bone marrow reserve: neutrophils ≥ 1.5 x 10^9/L and platelets ≥ 100 x 10^9/L

Exclusion Criteria

• Receiving concomitant cytotoxic or other antineoplastic treatment. Hormone replacement therapy is allowed, as are steroid antiemetics
• Clinical evidence of central nervous system metastases
• Active infection
• Cannot adequately be followed up for the duration of the study
• A second primary malignancy (except in situ carcinoma of the cervix or adequately treated basal cell carcinoma of the skin)
• Use of any investigational agent in the 3 weeks prior to inclusion
• Serious concomitant systematic disorders incompatible with the study
• Received more than one previous chemotherapy regimen or had prior gemcitabine treatment
• Patients with tumor of borderline malignancy
• Patients with estimated GFR ≤ 50 mL/min

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Primary Outcome Measures

Name	Time	Method
Time to progressive disease

Secondary Outcome Measures

Name	Time	Method
Duration of response
Response rate
Quality of Life
Survival time
Toxicity