Status:
COMPLETED
Taxol® in Monotherapy or in Combination With Topotecan or Carboplatin in Patients With Epithelial Ovarian Cancer in Early Relapse
Lead Sponsor:
ARCAGY/ GINECO GROUP
Conditions:
Ovarian Cancer
Fallopian Tube Cancer
Eligibility:
FEMALE
18+ years
Phase:
PHASE2
Brief Summary
This study will look at the efficacy and safety of weekly administration of paclitaxel (Taxol®) in monotherapy compared to paclitaxel in combination with topotecan or carboplatin in patients with ovar...
Detailed Description
The main purpose of this research study is to find out if treatment of early relapse of ovarian or fallopian tube or peritoneal cancer with paclitaxel (Taxol\*) weekly administered, in lower doses in ...
Eligibility Criteria
Inclusion
- Patients aged \> 18
- Histologically proven diagnosis of cancer of the ovary, the fallopian tube or peritoneum
- Peritoneal and/or nodes and/or visceral metastases
- Disease in progression under treatment or within 6 months after a first or second platinum-based line
- A period of 3 weeks between last chemotherapy and inclusion
- Measurable disease (Response Evaluation Criteria in Solid Tumors \[RECIST\] criteria) or cancer antigen (CA) 125 assessable disease (Gynecologic Cancer Intergroup \[GCIG\] criteria)
- ECOG performance status \< 2
- Life expectancy of at least 12 weeks
Exclusion
- Previously received weekly administration of paclitaxel chemotherapy
- Involved in a trial within the last 30 days
- Previously received a bone marrow autogreffe or irradiation of the abdomen within 5 years, due to intensive chemotherapy
- Prior diagnosis of malignancy
- History of ischemic cardiopathy, congestive heart failure (New York Heart Association \[NYHA\] \> 2), arrhythmia, hypertension, or significant valvulopathy
- Pre-existing motor or sensory neurologic pathology or symptoms National Cancer Institute (NCI) - Common Terminology Criteria for Adverse Events (CTCAE) grade \> 2
- Bone marrow, renal, or hepatic insufficiency
- Severe active infection or occlusive or sub-occlusive disease
- History of symptomatic brain metastases
- Fertile women not using adequate contraceptive methods
- Pregnant or breast feeding women
- Hypersensitivity to compounds chemically related to paclitaxel, topotecan, or carboplatin
Key Trial Info
Start Date :
April 1 2004
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
April 1 2009
Estimated Enrollment :
165 Patients enrolled
Trial Details
Trial ID
NCT00189566
Start Date
April 1 2004
End Date
April 1 2009
Last Update
February 25 2011
Active Locations (1)
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1
Hôpital Hotel Dieu
Paris, France, 75004