Radiation Therapy With or Without Thalidomide in Treating Patients With Brain Metastases

National Cancer Institute (NCI)

Status and phase: Completed; Phase 3

Conditions: Tumors Metastatic to Brain

Treatments: Radiation: radiation therapy; Procedure: quality-of-life assessment; Drug: thalidomide

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00033254

RTOG-BR-0118

NCI-2012-02461

U10CA021661 (U.S. NIH Grant/Contract)

CDR0000069268

Details and patient eligibility

About

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

Full description

OBJECTIVES:

I. Compare the overall survival of patients with multiple brain metastases treated with radiotherapy with or without thalidomide.

II. Compare the time to tumor progression in patients treated with these regimens.

III. Compare the time to neuro-cognitive progression in patients treated with these regimens.

IV. Compare the cause of death distribution in patients treated with these regimens.

V. Compare the frequency of toxic effects of these regimens in these patients. VI. 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.

Enrollment: 332 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

• Histologically confirmed extracranial primary malignancy

• Multiple brain metastases

• At least 1 measurable brain metastasis by MRI

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

• Performance status - Zubrod 0-1

• At least 8 weeks

• 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%*

• Bilirubin no greater than 1.5 mg/dL

• ALT no greater than 2 times normal

• Creatinine no greater than 1.5 mg/dL

• BUN no greater than 25 mg/dL

• No history of deep venous thrombosis

• 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

• No prior thalidomide

• 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)

• See Disease Characteristics

• No prior radiotherapy to the head or neck

• No prior radiosurgery

• Prior resection of brain metastases allowed

• No concurrent anticoagulant therapy

Trial design

Primary purpose: Treatment

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: None (Open label)

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332 participants in 2 patient groups

Arm I (radiation therapy)

Active Comparator group

Description:

Patients undergo radiotherapy once daily 5 days a week for 3 weeks.

Treatment:

Procedure: quality-of-life assessment

Radiation: radiation therapy

Arm II (radiation therapy, thalidomide)

Experimental group

Description:

Patients undergo radiotherapy as in arm I. Beginning on the first day of radiotherapy, patients receive oral thalidomide once daily.

Treatment:

Procedure: quality-of-life assessment

Drug: thalidomide

Radiation: radiation therapy