RATIONALE: Radiation therapy uses high-energy x-rays to damage tumor cells. Drugs such as thalidomide may stop the growth of brain metastases by stopping blood flow to the tumor. It is not yet known whether radiation therapy is more effective with or without thalidomide in treating brain metastases.

PURPOSE: Randomized phase III trial to compare the effectiveness of radiation therapy with or without thalidomide in treating patients who have brain metastases.

OBJECTIVES:

• Compare the overall survival of patients with multiple brain metastases treated with radiotherapy with or without thalidomide.
• Compare the time to tumor progression in patients treated with these regimens.
• Compare the time to neuro-cognitive progression in patients treated with these regimens.
• Compare the cause of death distribution in patients treated with these regimens.
• Compare the frequency of toxic effects of these regimens in these patients.
• Evaluate and compare the quality of life of patients treated with these regimens.

OUTLINE: This is a randomized, multicenter study. Patients are stratified according to recursive partitioning analysis class (I vs II) and planned chemotherapy after whole brain irradiation (yes vs no). Patients are randomized to 1 of 2 treatment arms.

• Arm I: Patients undergo radiotherapy once daily 5 days a week for 3 weeks.
• Arm II: Patients undergo radiotherapy as in arm I. Beginning on the first day of radiotherapy, patients receive oral thalidomide once daily. Treatment with thalidomide continues for 2 years in the absence of disease progression or unacceptable toxicity.

Quality of life is assessed at baseline, at completion of radiotherapy, and then every 2 months for 1 year.

Patients are followed every 2 months for 1 year, every 4 months for 1 year, every 6 months for 2 years, and then annually thereafter.

PROJECTED ACCRUAL: A total of 332 patients (166 per treatment arm) will be accrued for this study within 14.5 months.

• Drug: thalidomide
• Radiation: radiation therapy

• Corn BW, Moughan J, Knisely JP, Fox SW, Chakravarti A, Yung WK, Curran WJ Jr, Robins HI, Brachman DG, Henderson RH, Mehta MP, Movsas B. Prospective Evaluation of Quality of Life and Neurocognitive Effects in Patients with Multiple Brain Metastases Receiving Whole-Brain Radiotherapy with or without Thalidomide on Radiation Therapy Oncology Group (RTOG) Trial 0118. Int J Radiat Oncol Biol Phys. 2007 Dec 28; [Epub ahead of print]
• Knisely JP, Berkey B, Chakravarti A, Yung AW, Curran Jr WJ, Robins HI, Movsas B, Brachman DG, Henderson RH, Mehta MP. A Phase III Study of Conventional Radiation Therapy Plus Thalidomide versus Conventional Radiation Therapy for Multiple Brain Metastases (RTOG 0118). Int J Radiat Oncol Biol Phys. 2007 Dec 28; [Epub ahead of print]

DISEASE CHARACTERISTICS:

• Histologically confirmed extracranial primary malignancy
• Multiple brain metastases

• At least 1 measurable brain metastasis by MRI

  • More than 4.0 cm OR
  • Located in midbrain or brainstem (radiosurgery ineligible)

PATIENT CHARACTERISTICS:

Age:

• Over 18

Performance status:

• Zubrod 0-1

Life expectancy:

• At least 8 weeks

Hematopoietic:

• Absolute neutrophil count at least 1,500/mm^3
• Platelet count at least 100,000/mm^3
• Hemoglobin at least 11 g/dL*
• Hematocrit at least 35%* NOTE: * Transfusion and/or epoetin alfa allowed

Hepatic:

• Bilirubin no greater than 1.5 mg/dL
• ALT no greater than 2 times normal

Renal:

• Creatinine no greater than 1.5 mg/dL
• BUN no greater than 25 mg/dL

Cardiovascular:

• No history of deep venous thrombosis

Other:

• No sensory neuropathy grade 2 or greater
• No known AIDS
• No other major medical illness or psychiatric impairments that would preclude study therapy
• Not pregnant or nursing
• Negative pregnancy test
• Fertile patients must use effective barrier method of contraception during and for at least 4 weeks after study

PRIOR CONCURRENT THERAPY:

Biologic therapy:

• No prior thalidomide

Chemotherapy:

• More than 2 weeks since prior chemotherapy
• Concurrent chemotherapy allowed if more than 6 weeks past study entry (allowed during first 6 weeks of study if disease progression occurs)

Endocrine therapy:

• Not specified

Radiotherapy:

• See Disease Characteristics
• No prior radiotherapy to the head or neck
• No prior radiosurgery

Surgery:

• Prior resection of brain metastases allowed

Other:

• No concurrent anticoagulant therapy