Paclitaxel, Carboplatin, and Bevacizumab or Paclitaxel, Carboplatin, and Temsirolimus or Ixabepilone, Carboplatin, and Bevacizumab in Treating Patients With Stage III, Stage IV, or Recurrent Endometrial Cancer
NCT00977574 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 349
Last updated 2026-04-29
Summary
This randomized phase II trial studies paclitaxel, carboplatin, and bevacizumab or paclitaxel, carboplatin, and temsirolimus or ixabepilone, carboplatin, and bevacizumab to see how well they work in treating patients with stage III, stage IV, or recurrent endometrial cancer. Drugs used in chemotherapy, such as paclitaxel, carboplatin, and ixabepilone, work in different ways to stop the growth of tumor cells, either by killing the cells or by stopping them from dividing. Monoclonal antibodies, such as bevacizumab, may interfere with the ability of tumor cells to grow and spread. Temsirolimus may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. It is not yet known which treatment regimen is most effective in treating patients with endometrial cancer.
Conditions
- Endometrial Adenocarcinoma
- Endometrial Adenosquamous Carcinoma
- Endometrial Clear Cell Adenocarcinoma
- Endometrial Serous Adenocarcinoma
- Recurrent Malignant Uterine Corpus Neoplasm
- Stage IIIA Uterine Corpus Carcinoma or Carcinosarcoma by AJCC v7 Stage
- Stage IIIB Uterine Corpus Carcinoma or Carcinosarcoma by AJCC v7 Stage
- Stage IIIC Uterine Corpus Carcinoma or Carcinosarcoma by AJCC v7 Stage
- Stage IVA Uterine Corpus Carcinoma or Carcinosarcoma by AJCC v7 Stage
- Stage IVB Uterine Corpus Carcinoma or Carcinosarcoma by AJCC v7 Stage
Interventions
- BIOLOGICAL
-
Given IV
- DRUG
-
Given IV
- DRUG
-
Ixabepilone
Given IV
- OTHER
-
Laboratory Biomarker Analysis
Correlative studies
- DRUG
-
Given IV
- DRUG
-
Temsirolimus
Given IV
Sponsors & Collaborators
- collaborator OTHER
-
National Cancer Institute (NCI)
lead NIH
Principal Investigators
-
Carol Aghajanian · NRG Oncology
Study Design
- Allocation
- RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- FEMALE
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2009-09-14
- Primary Completion
- 2015-01-31
- Completion
- 2027-03-06
Countries
- United States
Study Locations
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