Status:
COMPLETED
Second-Line Treatment for Patients With Platinum-Sensitive Ovarian Cancer
Lead Sponsor:
Duke University
Collaborating Sponsors:
Aventis Pharmaceuticals
Conditions:
Ovarian Cancer
Eligibility:
FEMALE
18+ years
Phase:
PHASE2
Brief Summary
The purpose of this study is to compare the progression-free survival of two treatment regimens for relapsed ovarian cancer.
Detailed Description
Primary Objective The primary objective of the study is to compare the progression-free survival of two treatment regimens: Taxotere® 30 mg/m2 IV on Days 1 and 8, combined with carboplatin AUC 6 IV ...
Eligibility Criteria
Inclusion
- Pathologically confirmed epithelial ovarian cancer, peritoneal serous cancer, or tubal carcinoma.
- The patient's tumor is platinum-sensitive, which means that the patient had a complete response to front-line treatment with a platinum compound and had a treatment-free interval without clinical evidence of progressive disease for greater than 6 months.
- The patient has received one and only one prior chemotherapy regimen for the treatment of this malignancy. Prior treatment with paclitaxel and/or a platinum compound is allowed. Patients who have received consolidation treatment are allowed. Prior treatment with Taxotere® is not allowed.
- o Consolidation therapy is allowed including a different cytotoxic agent than the agent used in the front-line regimen, intraperitoneal therapy, biologic therapy, and immunotherapy.
- Patients may have received one prior regimen with a biologic therapy, either combined with cytotoxic therapy in the front-line setting, or as a single-agent for this recurrence. The biologic therapy must be discontinued at least three weeks prior to registration.
- Measurable or evaluable disease either by radiologic imaging, or physical exam, or by measurement of CA125 \< 70 on two occasions at least one week apart.
- At least 3 weeks since radiotherapy, with full recovery. The measurable disease must be completely outside the radiation portal.
- At least 3 weeks since major surgery, with full recovery. Patients who have undergone a secondary tumor debulking or cytoreductive surgery for this malignancy are excluded.
- Eastern Cooperative Oncology Group (ECOG) performance status \< 2.
- Age \> 18 years.
- Absolute neutrophil count \> 1,500/mm3; platelet count \> 100,000/mm3; Hemoglobin \> 8.0 g/dl
- Serum bilirubin Within Normal Limits (WNL); AST or ALT and Alkaline Phosphatase must be within the range allowing for eligibility.
- If there is childbearing potential, a serum pregnancy test must be negative.
- Patients of childbearing potential must be willing to consent to using effective contraception while on treatment and for three months following the completion of treatment.
- Informed consent has been obtained.
Exclusion
- Prior treatment with Taxotere®.
- Concurrent immunotherapy or hormonal therapy for the specific purpose of treatment for the disease. Any hormonal therapy directed at the malignant tumor must be discontinued at least one week prior to enrollment in order for the patient to be eligible to participate in this trial. Continuation of Hormone Replacement therapy is permitted.
- Serious concurrent medical or psychiatric illness, including serious active infection.
- Peripheral neuropathy \> grade 2.
- History of other malignancy within the last 5 years, except for basal cell skin carcinoma.
- The patient is pregnant or nursing.
- Patients with a history of severe hypersensitivity reaction to cisplatin, carboplatin, mannitol, or drugs formulated with Polysorbate 80.
- Secondary debulking for this recurrence.
Key Trial Info
Start Date :
October 1 2003
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
October 1 2009
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT00090610
Start Date
October 1 2003
End Date
October 1 2009
Last Update
February 25 2015
Active Locations (19)
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1
Florida Gynecologic Oncology
Fort Myers, Florida, United States, 33901
2
Jupiter Medical Center-Gynecology Oncology and Gynecology
Jupiter, Florida, United States, 33458
3
Florida Hospital/Gyn/Onc Department
Orlando, Florida, United States, 32804
4
Hematology-Onc. Assoc. of The Quad Cities
Bettendorf, Iowa, United States, 52722