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OncoMatch/Clinical Trials/NCT04623931

Chemotherapy and Radiation Therapy for the Treatment of IDH Wildtype Gliomas or Non-histological (Molecular) Glioblastomas

Is NCT04623931 recruiting? Yes, currently enrolling (May 2026). This Phase 2 trial studies Temozolomide for anaplastic astrocytoma, idh-wildtype.

Phase 2RecruitingM.D. Anderson Cancer CenterNCT04623931Data as of May 2026

Treatment: TemozolomideThis phase II trial studies how well temozolomide and radiation therapy work in treating patients with IDH wildtype historically lower grade gliomas or non-histological molecular glioblastomas. Radiation therapy uses high-energy x-rays to kill tumor cells and shrink tumors. Giving chemotherapy with radiation therapy may kill more tumor cells. Drugs used in chemotherapy, such as temozolomide, work in different ways to stop the growth of tumor cells, either by killing the cells, by stopping them from dividing, or by stopping them from spreading. The goal of this clinical research study is to compare receiving new radiation therapy doses and volumes to the prior standard treatment for patients with historically grade II or grade III IDH wild-type gliomas, which may now be referred to as IDH wildtype molecular glioblastomas at some institutions. Receiving temozolomide in combination with radiation therapy may also help to control the disease.

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Extracted eligibility criteria

Cancer type

Glioblastoma

Biomarker criteria

Required: IDH1 wild-type

Required: IDH2 wild-type

Disease stage

Required: Stage II, III (WHO)

Excluded: Stage I, IV

Historical grade II and III gliomas

Prior therapy

No prior treatment (treatment-naive required)
Max 0 prior lines

Cannot have received: cranial radiotherapy

Prior cranial radiotherapy or radiotherapy to the head and neck where potential field overlaps would exist

Cannot have received: chemotherapy for any brain tumor

Prior chemotherapy or radiotherapy for any brain tumor

Lab requirements

Blood counts

Absolute neutrophil count (ANC) ≥ 1,500 cells/mm^3; Platelets ≥ 100,000 cells/mm^3; Hemoglobin ≥ 10.0 g/dl (transfusion/intervention allowed)

Kidney function

Blood urea nitrogen (BUN) < 30 mg/dl; Serum creatinine < 1.5 mg/dl

Liver function

Bilirubin ≤ 1.5 upper limit of normal (ULN); ALT and AST ≤ 3 x ULN

ANC ≥ 1,500 cells/mm^3; Platelets ≥ 100,000 cells/mm^3; Hemoglobin ≥ 10.0 g/dl; Bilirubin ≤ 1.5 ULN; ALT and AST ≤ 3 x ULN; BUN < 30 mg/dl; Serum creatinine < 1.5 mg/dl

Structured fields extracted by AI. May contain errors — verify against the official protocol.

US trial sites

  • M D Anderson Cancer Center · Houston, Texas

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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