OncoMatch/Clinical Trials/NCT07750457
Proton vs. Photon Radiotherapy for Patients With WHO Grade 2-3 Glioma
Is NCT07750457 recruiting? Yes, currently enrolling (Sep 2026). This NA trial studies non-drug interventions for glioma.
Patients with grade 2 and 3 gliomas who received photon radiation therapy as part of their standard treatment are at risk of developing cognitive impairments, depending on the tumor's location and the size of the target volume. The extent to which these are caused in individual cases by the brain tissue within the target volume, which is necessarily exposed to a high dose, or whether they can be modified by differences in the exposure of surrounding brain regions exposed to low or moderate doses, is unknown. With the help of proton therapy, the risk of neurocognitive dysfunction could potentially be reduced by decreasing the brain volumes outside the target volume that are exposed to radiation therapy and receive a low dose. Based on current knowledge of relative biological effectiveness, the efficacy of proton therapy on the tumor compared to photon therapy can be considered equivalent with lower levels of uncertainty. In the present study, the impact of photon irradiation versus proton irradiation on neurocognition will now be directly compared. A bicentric, randomized study will investigate whether treating patients with WHO Grade 2 and 3 gliomas with proton radiation results in a different temporal course of neurocognitive function after treatment compared to photon radiation therapy.
Check if I qualifyExtracted eligibility criteria
Cancer type
Glioblastoma
Biomarker criteria
Required: IDH1 mutation
IDH1/2 mutation
Required: IDH2 mutation
IDH1/2 mutation
Disease stage
Required: Stage WHO GRADE 2, WHO GRADE 3 (other)
Excluded: Stage WHO GRADE 4
WHO Grade 2 or 3 glioma
Prior therapy
Cannot have received: radiation therapy to the head or head and neck region
Previous radiation therapy to the head or head and neck region
Cannot have received: chemotherapy due to a CNS neoplasm
Previous chemotherapy due to a CNS neoplasm
Lab requirements
Blood counts
Absolute neutrophil count 1,500/mm9, Platelet count 100,000/mm9, Hemoglobin (Hb) level > 10 g/dL
Kidney function
Creatinine level 1.5 times the upper limit of normal
Liver function
Total bilirubin level 1.5 times the upper limit of normal, AST and ALT levels 3 times the upper limit of normal
Laboratory values: Absolute neutrophil count 1,500/mm9, Platelet count 100,000/mm9, Hemoglobin (Hb) level > 10 g/dL, Total bilirubin level 1.5 times the upper limit of normal, AST and ALT levels 3 times the upper limit of normal, Creatinine level 1.5 times the upper limit of normal
Structured fields extracted by AI. May contain errors — verify against the official protocol.
Frequently asked questions
Is NCT07750457 currently recruiting?
Yes, this trial is currently recruiting patients.
Are there prior therapy exclusions?
Yes. Prior radiation therapy to the head or head and neck region, chemotherapy due to a CNS neoplasm disqualifies patients from enrollment.
Does this trial require IDH1?
Yes, IDH1 mutation is a required biomarker for enrollment.
Does this trial require IDH2?
Yes, IDH2 mutation is a required biomarker for enrollment.
What disease stage is eligible?
Stage WHO GRADE 2 or WHO GRADE 3 is required.
Could you qualify for this trial?
Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.
Check if I qualifyRelated pages