Thalidomide in Treating Patients With Gynecologic Sarcomas
Endometrial Cancer, Sarcoma
About this trial
This is an interventional treatment trial for Endometrial Cancer focused on measuring stage I uterine sarcoma, stage II uterine sarcoma, stage III uterine sarcoma, stage IV uterine sarcoma, recurrent uterine sarcoma, uterine carcinosarcoma, uterine leiomyosarcoma, endometrial stromal sarcoma
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically or cytologically confirmed sarcoma or carcinosarcoma (mixed mesodermal tumors) of gynecologic origin not amenable to resection or radiotherapy Measurable disease Lesions accurately measured in at least 1 dimension of at least 20 mm in longest diameter with conventional techniques or at least 10 mm with helical CT scan Histologically or cytologically confirmed neoplastic nature if solitary lesion No nonmeasurable disease, defined as: Bone lesions Leptomeningeal disease Ascites Pleural/pericardial effusion Inflammatory breast disease Lymphangitis cutis/pulmonis Unconfirmed abdominal masses not followed by imaging techniques Cystic lesions Documented recurrence or persistence following appropriate surgery, radiotherapy, and/or chemotherapy Postmenopausal or status post hysterectomy PATIENT CHARACTERISTICS: Age: Not specified Performance status: ECOG 0-1 Life expectancy: Not specified Hematopoietic: Granulocyte count at least 1,000/mm^3 Platelet count at least 50,000/mm^3 Hepatic: Bilirubin normal Transaminases less than 2.5 times upper limit of normal Renal: Creatinine less than 1.5 mg/dL Other: No grade 2 or greater peripheral neuropathy No medical or social factors that would preclude study, including inability to take oral medication No other serious illness requiring immediate therapy Not pregnant PRIOR CONCURRENT THERAPY: Biologic therapy: Not specified Chemotherapy: See Disease Characteristics At least 4 weeks since prior chemotherapy (6 weeks since mitomycin or nitrosoureas) Endocrine therapy: Not specified Radiotherapy: See Disease Characteristics At least 4 weeks since prior radiotherapy No concurrent radiotherapy Surgery: See Disease Characteristics Other: At least 30 days since any prior noncytotoxic experimental antiemetic or antifungal investigational drug
Sites / Locations
- Cancer Center of Albany Medical Center
- Albert Einstein Clinical Cancer Center
- North Shore University Hospital
- St. Vincent's Comprehensive Cancer Center
- NYU School of Medicine's Kaplan Comprehensive Cancer Center
- St. Luke's-Roosevelt Hospital Center - Roosevelt Division
- New York Weill Cornell Cancer Center at Cornell University
- Mount Sinai School of Medicine
- New York Medical College
- University of Wisconsin Comprehensive Cancer Center