Gefitinib and Radiation Therapy in Treating Patients With Glioblastoma Multiforme

National Cancer Institute (NCI)

Status and phase: Completed; Phase 2; Phase 1

Conditions: Adult Glioblastoma; Adult Giant Cell Glioblastoma; Adult Gliosarcoma

Treatments: Other: laboratory biomarker analysis; Drug: gefitinib; Radiation: radiation therapy

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT00052208

CDR0000069330

NCI-2013-00849

RTOG-0211

RTOG-BR-0211

U10CA021661 (U.S. NIH Grant/Contract)

Details and patient eligibility

About

This phase I/II trial studies the side effects and best dose of gefitinib when given together with radiation therapy and to see how well it works in treating patients with glioblastoma multiforme. Gefitinib may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth. Radiation therapy uses high energy x rays to kill tumor cells. Giving gefitinib together with radiation therapy may be an effective treatment for glioblastoma multiforme.

Full description

PRIMARY OBJECTIVES:

I. To identify the maximum tolerated dose of ZD 1839 (gefitinib) when given concurrently with cranial radiotherapy.

II. To determine if ZD 1839, given orally on a daily basis starting at the time of conventional radiation therapy (RT), may improve the overall survival of adults with newly-diagnosed supratentorial glioblastoma multiforme, compared with historical controls, stratifying by epidermal growth factor receptor (EGFR) status.

III. To determine, in a multi-institutional setting, the feasibility and toxicity of prescribing ZD 1839.

SECONDARY OBJECTIVES:

I. Whether ZD 1839 also improves progression-free survival in these patients.

OUTLINE: This is a phase I, dose-escalation study of gefitinib followed by a phase II study.

Patients receive gefitinib orally (PO) once daily (QD) for 7 weeks. Beginning 1 week after initiation of gefitinib, patients undergo radiation therapy QD 5 days a week for 6 weeks. Treatment with gefitinib continues for up to 18 months in the absence of disease progression or unacceptable toxicity.

After completion of study treatment, patients are followed up every 4 months for 1 year, every 6 months for 2 years, and annually thereafter.

Enrollment: 158 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Histopathologically confirmed glioblastoma multiforme (with areas of necrosis)
• Diagnosis must be made by surgical biopsy or excision
• The tumor must be supratentorial in location
• The patient must have recovered from the effects of surgery, post-operative infection, or other complications before study entry
• Radiotherapy must begin =< five weeks after surgery, and Iressa (gefitinib) must begin one week prior to radiotherapy
• Patients must have an estimated survival of at least 8 weeks
• Zubrod performance status of 0-1
• A diagnostic contrast-enhanced magnetic resonance imaging (MRI) or computed tomography (CT) scan must be performed preoperatively and postoperatively prior to the initiation of radiotherapy; preoperative and postoperative scans must be the same type
• Patients diagnosed only by stereotactic biopsy do not require the postoperative scan
• Patients unable to undergo magnetic resonance (MR) imaging because of non-compatible devices can be enrolled, provided pre and postoperative CT scans are obtained and are of sufficient quality
• Hemoglobin >= 10 grams
• Absolute neutrophil count >= 1500 (ANC) per mm^3
• Platelets >= 100,000 per mm^3
• Blood urea nitrogen (BUN) =< 25 mg
• Creatinine =< 1.5 mg
• Bilirubin =< 2.0 mg
• Serum glutamate pyruvate transaminase (SGPT) or serum glutamic oxaloacetic transaminase (SGOT) =< 2 x normal range
• Patients must consent to submission of their tissue/serum
• The patient must sign a study-specific informed consent prior to study entry; if the patient's mental status precludes his/her giving informed consent, written informed consent may be given by the responsible family member

Exclusion criteria

• Recurrent or multifocal malignant gliomas
• Metastases detected below the tentorium or beyond the cranial vault
• Major medical illnesses or psychiatric impairments which, in the investigator's opinion, will prevent administration or completion of protocol therapy
• Previous radiotherapy to the head or neck (except for T1 glottic cancer), resulting in overlap of radiation fields
• Active connective tissue disorders, such as lupus or scleroderma which, in the opinion of the treating physician, may put the patient at high risk for radiation toxicity
• Previous malignancies, except for non-melanomatous skin cancers and carcinoma in situ of the uterine cervix or bladder, unless disease-free for >= 3 years
• Prior chemotherapy or radiosensitizers for cancers of the head and neck region
• Patients with known acquired immune deficiency (AIDS); patients with AIDS require complex therapeutic regimens; the pharmacokinetic interactions of these regimens with ZD 1839 are unknown and therefore, pose a safety risk related to excess toxicity or interference with anti-viral effectiveness
• Patients with known multiple sclerosis, as these patients may have decreased tolerance for radiation therapy to the brain
• Pregnant or lactating women, due to possible adverse effects on the developing fetus or infant due to study drug
• Patients treated on any other clinical protocols within 30 days prior to study entry or during participation in the study

Trial design

Primary purpose: Treatment

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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158 participants in 1 patient group

Treatment (gefitinib, radiation therapy)

Experimental group

Description:

Patients receive gefitinib PO QD for 7 weeks. Beginning 1 week after initiation of gefitinib, patients undergo radiation therapy QD 5 days a week for 6 weeks. Treatment with gefitinib continues for up to 18 months in the absence of disease progression or unacceptable toxicity.

Treatment:

Radiation: radiation therapy

Drug: gefitinib

Other: laboratory biomarker analysis