Thalidomide in Treating Patients With Metastatic Neuroendocrine Tumors
Gastrointestinal Carcinoid Tumor, Islet Cell Tumor, Lung Cancer
About this trial
This is an interventional treatment trial for Gastrointestinal Carcinoid Tumor focused on measuring metastatic gastrointestinal carcinoid tumor, recurrent gastrointestinal carcinoid tumor, gastrinoma, insulinoma, recurrent islet cell carcinoma, WDHA syndrome, somatostatinoma, pancreatic polypeptide tumor, glucagonoma, pulmonary carcinoid tumor
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed low-grade neuroendocrine tumors Carcinoid tumors Islet cell tumors Metastatic disease Progression of disease within past 4 weeks by radiological evidence At least 1 bidimensionally measurable lesion by CT scan or MRI Bone metastasis not considered measurable if only site of disease No active brain metastases PATIENT CHARACTERISTICS: Age: Not specified Performance status: Karnofsky 70-100% Life expectancy: More than 3 months Hematopoietic: WBC at least 3,000/mm^3 Absolute neutrophil count at least 1,500/mm^3 Platelet count at least 100,000/mm^3 Hepatic: Bilirubin normal AST no greater than 2.5 times upper limit of normal (ULN) Renal: Creatinine no greater than 1.5 times ULN OR Creatinine clearance at least 50 mL/min Other: Not pregnant or nursing Negative pregnancy test Fertile patients must use 2 forms of effective contraception for 4 weeks before, during, and for 4 weeks after study No grade 2 or greater neuropathy No other clinical circumstances that would preclude study No other prior malignancy except: Non-melanoma skin cancer Other cancer that has been curatively treated, has had no evidence of recurrence within the past 5 years, and is at low risk for recurrence PRIOR CONCURRENT THERAPY: Biologic therapy: No prior thalidomide No concurrent interferon Chemotherapy: No concurrent chemotherapy Endocrine therapy: Not specified Radiotherapy: At least 4 weeks since prior radiotherapy No concurrent radiotherapy Surgery: At least 4 weeks since prior major surgery Other: No more than 1 prior systemic therapy regimen At least 4 weeks since prior systemic therapy regimen No other concurrent therapeutic agent
Sites / Locations
- Memorial Sloan-Kettering Cancer Center