Temozolomide and Thalidomide in Treating Patients With Stage III or Stage IV Melanoma

• Status: Completed
• Trial end date: 2004-08-01
• Target enrollment: 0
• Participant gender: All

Summary

RATIONALE: Drugs used in chemotherapy use different ways to stop tumor cells from dividing so they stop growing or die. Thalidomide may stop the growth of melanoma by stopping blood flow to the tumor. Combining chemotherapy with thalidomide may kill more tumor cells.

PURPOSE: Phase I/II trial to study the effectiveness temozolomide plus thalidomide in treating patients who have stage III or stage IV melanoma that cannot be removed during surgery.

• Phase: Phase 1/Phase 2
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: Memorial Sloan Kettering Cancer Center
• Collaborator: National Cancer Institute (NCI)
• Treatments: Temozolomide; Thalidomide

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed metastatic malignant melanoma that is considered unresectable

• Stage III or IV ocular, mucosal, or cutaneous melanoma

• Measurable disease

• No CNS disease (phase I only)

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Performance status:

• Karnofsky 70-100%

Life expectancy:

• Not specified

Hematopoietic:

• Absolute granulocyte count at least 1,500/mm^3

• Platelet count at least 150,000/mm^3

Hepatic:

• Bilirubin no greater than 1.5 times upper limit of normal (ULN)

• SGOT/SGPT no greater than 3 times ULN

• Alkaline phosphatase no greater than 3 times ULN

Renal:

• Creatinine no greater than 1.5 times ULN

Cardiovascular:

• No history of active angina

• No myocardial infarction within past 6 months

• No history of significant ventricular arrhythmia requiring medication with antiarrhythmics

Other:

• Not pregnant or nursing

• Negative pregnancy test

• Fertile patients must use effective barrier contraception during and for 4 weeks before and after study

• No frequent vomiting or medical condition that could interfere with oral medication intake (e.g., partial bowel obstruction)

• No preexisting neurotoxicity grade 2 or greater

• No serious concurrent infections treated with antibiotics

• No nonmalignant medical illnesses that are uncontrolled or whose control may be jeopardized by the complications of this study

• No psychiatric disorders that would preclude study compliance

• No other medical condition or reason that would preclude study

• No other malignancy within the past 2 years except:

• Nonmelanoma skin cancer

• Carcinoma in situ of the cervix

• History of T1a or b prostate cancer detected incidentally at TURP and comprising less than 5% of resected tissue with PSA normal since TURP

• No AIDS related illness

• HIV negative

PRIOR CONCURRENT THERAPY:

• Recovered from prior therapy

Biologic therapy:

• At least 4 weeks since prior biologic therapy

• At least 4 weeks since prior immunotherapy

• No concurrent immunotherapy

Chemotherapy:

• No prior systemic chemotherapy for metastatic melanoma

• No other concurrent chemotherapy

Endocrine therapy:

• Not specified

Radiotherapy:

• At least 4 weeks since prior radiotherapy, interstitial brachytherapy, or radiosurgery

• At least 3 weeks since prior radiotherapy to the brain if brain metastases from melanoma

• Prior radiotherapy to only indicator lesion allowed provided recent evidence of disease progression at that site

• No concurrent radiotherapy

Surgery:

• At least 2 weeks since prior surgery requiring general anesthesia