Temozolomide and Thalidomide in Treating Patients With Metastatic, Locally Advanced, or Unresectable Leiomyosarcoma

• Status: Unknown status
• Trial end date: 1969-12-31
• 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 cancer by stopping blood flow to the tumor. Combining temozolomide with thalidomide may kill more tumor cells.

PURPOSE: Phase II trial to study the effectiveness of combining temozolomide with thalidomide in treating patients who have metastatic, locally advanced, or unresectable leiomyosarcoma.

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

Details

• Lead Sponsor: Herbert Irving Comprehensive Cancer Center
• Collaborator: National Cancer Institute (NCI)
• Treatments: Dacarbazine; Temozolomide; Thalidomide

Criteria

DISEASE CHARACTERISTICS:

• Histologically confirmed leiomyosarcoma

• Metastatic, locally advanced, or unresectable

• Ineligible for other high priority national or institutional study

• At least 1 unidimensionally measurable lesion documented on radiologic study

• At least 2 cm by 2 cm

• Not previously irradiated unless disease progression at the site is evident

• No brain metastases

PATIENT CHARACTERISTICS:

Age:

• 18 and over

Performance status:

• SWOG 0-2

Life expectancy:

• More than 2 months

Hematopoietic:

• WBC greater than 3,000/mm^3

• Neutrophil count at least 1,500/mm^3

• Platelet count greater than 70,000/mm^3

• Hemoglobin at least 10 g/dL

Hepatic:

• Bilirubin less than upper limit of normal (ULN)

• SGOT or SGPT less than 1.5 times ULN*

• Alkaline phosphatase less than 2 times ULN* NOTE: * Less than 5 times ULN if documented liver disease

Renal:

• Creatinine less than 1.5 times normal OR

• Creatinine clearance greater than 60 mL/min

• BUN less than 1.5 times normal

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 therapy

• No acute infection requiring systemic antibiotics

• No frequent vomiting or medical condition that would preclude intake of oral medication (e.g., partial bowel obstruction)

• No other serious medical or psychiatric illness that would preclude study participation

• No prior malignancy except curatively treated carcinoma in situ of the cervix or skin cancer

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• Not specified

Chemotherapy:

• At least 4 weeks since prior chemotherapy

• No more than 3 prior systemic chemotherapy regimens for metastatic, locally advanced, or unresectable leiomyosarcoma

• Prior dacarbazine allowed

Endocrine therapy:

• Not specified

Radiotherapy:

• See Disease Characteristics

• At least 4 weeks since prior radiotherapy

• No prior radiotherapy to 50% or more of bone marrow

• Concurrent radiotherapy for local control or palliative therapy for painful bony or soft tissue lesion allowed

Surgery:

• At least 4 weeks since prior surgery and recovered

Other:

• Recovered from all prior therapies

• No other concurrent investigational drugs