Clinical Trial Finder

DISEASE CHARACTERISTICS:

• - Histologically confirmed supratentorial grade IV astrocytoma (glioblastoma multiforme) by biopsy or resection within the past 3 months.

PATIENT CHARACTERISTICS:

• - Karnofsky performance status ≥ 60% - Absolute neutrophil count ≥ 1500/mm^3.

• - Platelet count ≥ 100,000/mm^3.

• - Bilirubin ≤ 1.5 mg/dL.

• - Transaminases ≤ 4 times above the upper limits of the institutional normal.

• - Creatinine ≤ 1.7 mg/dL.

• - Not pregnant or breast-feeding.

• - Patients must agree to follow acceptable birth control methods to avoid conception.

• - Negative pregnancy test.

• - Patients must have a Mini Mental State Exam score of ≥ 15.

• - No serious concurrent infection or medical illness which would jeopardize the ability of the patient to receive the treatment outlined in this protocol with reasonable safety.

• - Patients with a concurrent or prior malignancy are ineligible unless they are patients with curatively treated carcinoma-in-situ or basal cell carcinoma of the skin.

• - Patients who have been free of disease (any prior malignancy) for ≥ five years are eligible for this study.

• - Patients requiring ongoing therapy for psychoses with antipsychotic medications at the time of enrollment will be ineligible.

PRIOR CONCURRENT THERAPY:

• - Patients must not have received prior radiation therapy, chemotherapy, immunotherapy or therapy with biologic agent (including immunotoxins, immunoconjugates, antisense, peptide receptor antagonists, interferons, interleukins, TIL, LAK or gene therapy), or hormonal therapy for their brain tumor.

• - Prior glucocorticoid therapy is allowed.

• - Patients must be willing to forego other cytotoxic and non-cytotoxic drug therapy against the tumor while being treated with poly ICLC plus temozolomide on this protocol.

• - No other concurrent therapy for their tumor (i.e., chemotherapeutics or investigational agents) - Patients who have received prior Gliadel wafers are not eligible for this study.

- No concurrent prophylactic filgrastim (G-CSF) - No concurrent electron, particle, implant, or stereotactic radiosurgery boost

OBJECTIVES: Primary.

• - Evaluate the safety and efficacy of radiation plus low-dose temozolomide followed by adjuvant temozolomide and intramuscular poly ICLC for adult patients with newly diagnosed glioblastoma multiforme.

Secondary.

• - Estimate the frequency of toxicity associated with this treatment regimen.

OUTLINE: This is an open-label, multicenter study.

• - Induction chemoradiotherapy: Patients undergo radiotherapy once daily, 5 days a week, for 6 weeks.

During the same 6 weeks, patients also receive oral temozolomide once daily. Four weeks later, patients are evaluated for disease progression. Patients with progressive disease are removed from the study. Patients with no progressive disease proceed to maintenance therapy.

• - Maintenance therapy: Patients receive oral temozolomide once daily on days 1-5 (week 1).

Patients also receive poly ICLC intramuscularly three times a week in weeks 2-8. Courses repeat every 9 weeks in the absence of disease progression or unacceptable toxicity. After completion of study therapy, patients are followed every 2 months for survival. PROJECTED ACCRUAL: A total of 96 patients will be accrued for this study.

Arms

Experimental: Treatment Arm

RT + TMZ 6wks, followed by poly ICLC, temozolomide, radiation: radiation therapy

Interventions

Drug: - poly ICLC

20 mcg/kg 3x each week (Maintenance cycles)

Drug: - temozolomide

daily 75mg/m2 6wks concomitant therapy Wk 1 - days 1-5 150-200 mg/m2 maintenance cycles (adjuvant)

Radiation: - radiation therapy

RT: 60 Gy (6 weeks) concomitant therapy