OncoMatch/Clinical Trials/NCT05331521
A Clinical Study to Improve Brain Function and Quality of Life of Patients With Newly Diagnosed Brain Tumors (Gliomas).
Is NCT05331521 recruiting? Yes, currently enrolling (May 2026). This Phase 3 trial studies multiple treatments including CETEG and PCV for oligodendroglioma.
Treatment: CETEG · PCV — Oligodendrogliomas in the novel edition of the Central Nervous System (CNS) World Health Organization (WHO) classification are now molecularly defined by isocitrate dehydrogenase (IDH)1 or IDH2 mutations and 1p/19q co-deletion. The prognosis of these molecularly defined tumors is to be determined in new series since survival data from older histology-based studies and population-based registries are confounded by the inclusion of 20-70% not molecularly matching subsets. Also, the optimal treatment is a matter of ongoing investigations. An extensive, but safe surgery is associated with improved outcome as is the addition of chemotherapy with procarbazine, CCNU (lomustine), and vincristine (PCV) to the partial brain radiotherapy (RT). However, the exact timing of postsurgical therapy especially for tumors of the WHO grade 2 and acknowledging some variability in grading as well as the choice of chemotherapy, temozolomide instead of PCV (CODEL: NCT00887146 randomizing CNS WHO grade 2 and 3 oligodendrogliomas to chemoradiation(CHRT)therapy with PCV or with temozolomide) or the need for primary radiotherapy RT are subjects of clinical studies (POLCA: NCT02444000 randomizing patients with newly diagnosed CNS WHO grade 3 oligodendrogliomas to standard CHRT with PCV or PCV alone). Given the young age of patients with CNS WHO grade 2 and 3 oligodendrogliomas and the relevant risk of neurocognitive, functional and quality-of-life impairment with the current aggressive standard of care treatment, chemoradiation with PCV, of the tumor located in the brain optimizing care is the major challenge. NOA-18/IMPROVE CODEL aims at improving qualified overall survival (qOS) for adult patients with CNS WHO grade 2 and 3 oligodendrogliomas by randomizing between standard chemoradiation with up to six six-weekly cycles with PCV and six six-weekly cycles with lomustine and temozolomide (CETEG), thereby delaying radiotherapy (RT) and adding the chemoradiotherapy (CHRT) concept at progression after initial radiation-free chemotherapy, allowing for an effective salvage treatment and delaying potentially deleterious side effects. QOS represents a new concept and is defined as OS without functional and/or cognitive and/or quality of life (QOL) deterioration regardless whether tumor progression or toxicity is the main cause.
Check if I qualifyExtracted eligibility criteria
Cancer type
Glioblastoma
Biomarker criteria
Required: 19Q co-deletion
Required: 1P co-deletion
Required: IDH1 mutation
Required: IDH2 mutation
Disease stage
Required: Stage WHO GRADE 2, WHO GRADE 3 (WHO CNS)
WHO grade 2 or 3 glioma
Prior therapy
Cannot have received: anti-cancer therapy
Exception: History of low-grade glioma that did not require prior treatment with chemotherapy or radiotherapy is not an exclusion criterion.
Any prior anti-cancer therapy or co-administration of anti-cancer therapies other than those administered/allowed in this study.
Lab requirements
Blood counts
Hb, WBC, neutrophils, or platelets (≥ Grade 2 CTCAE v5.0)
Kidney function
serum creatinine (≥ Grade 2 CTCAE v5.0)
Liver function
ALT or AST (≥ Grade 2 CTCAE v5.0) confirmed on two consecutive measurements; impaired excretory function (e.g., hyperbilirubinemia) or synthetic function or other conditions of decompensated liver disease such as coagulopathy, hepatic encephalopathy, hypoalbuminemia, ascites, and bleeding from esophageal varices (≥ Grade 2 CTCAE v5.0); acute viral or active autoimmune, alcoholic, or other types of acute hepatitis.
Abnormal (≥ Grade 2 CTCAE v5.0 laboratory values for hematology (Hb, WBC, neutrophils, or platelets), liver (serum bilirubin, ALT, or AST) or renal function (serum creatinine).
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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