A PHASE III RANDOMIZED TRIAL OF GEMCITABINE PLUS DOCETAXEL FOLLOWED BY DOXORUBICIN V. OBSERVATION FOR UTERUS-LIMITED, HIGH GRADE UTERINE LEIOMYOSARCOMA
- Conditions
- leiomyosarcomauterine10038597
- Registration Number
- NL-OMON41992
- Lead Sponsor
- European Organisation for Research in Treatment of Cancer (EORTC)
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Withdrawn
- Sex
- Not specified
- Target Recruitment
- 18
Patients with a high risk of uterine leiomyosarcoma FIGO stage I.
Institutional pathology review of leiomyosarcoma
Al patients must be no longer than 12 weeks (3 months) from surgical resection of cancer at the time of enrollment on study.
Age > 18 years
Written informed consent
Patient who had prior therapy with docetaxel or gemcitabine or doxorubicine
Patient with a history of malignancy being present within the last 5 years
Patient with a history of severe hypersensitivity reaction to anthracenedione/anthracyclines or drugs containing polysorbate 80 excipients are not allowed to participate in the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method <p>To determine whether overall survival of patients with uterus-limited<br /><br>high-grade leiomyosarcoma is superior among patients assigned to<br /><br>treatment with adjuvant gemcitabine plus docetaxel followed by<br /><br>doxorubicin compared to patients assigned to observation.</p><br>
- Secondary Outcome Measures
Name Time Method <p>To determine whether treatment with adjuvant gemcitabine plus docetaxel<br /><br>followed by doxorubicin improves recurrence-free survival of patients<br /><br>with uterus-limited high-grade leiomyosarcoma compared to observation.<br /><br><br /><br><br /><br>To explore the impact of potential predictors of recurrence or death such<br /><br>as patient age, and institution reported tumor size, cervix involvement (yes<br /><br>or no), and mitotic rate.</p><br>