Observational studyNeurology2025
Characteristics and Outcomes of Patients With IDH-Mutant Grade 2 and 3 Gliomas After Deferred or Adjuvant Radiotherapy.
Observational study in Neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
6 citing papers in PubMed.
- IDH-genotype-linked kinase rewiring accompanies enhanced therapeutic response to dual-drug ferritin nanocages in high-grade glioma.Materials today. Bio · 2026Article
- Contemporary practice patterns in IDH-mutant glioma management: a multidisciplinary multi-institutional survey.Journal of neuro-oncology · 2026Article
- The future of neurosurgical oncology lies in cognitive neurosciences: understanding brain processing is much more valuable than surgical technology.Frontiers in oncology · 2026Article
- Health-related quality of life and cognition in long-term oligodendroglioma survivors: A landmark study.Neuro-oncology · 2025Article
- Low tumour burden is associated with observation after surgery in patients with grade 2 astrocytoma and oligodendroglioma: results from the prospective multicentre LoG-Glio registry.Journal of neuro-oncology · 2025Article
- The role of a multidisciplinary clinic for management of patients with IDH mutant gliomas.Frontiers in oncology · 2025Article
Corrections and comments
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Authors and funding
5 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
BACKGROUND AND
objectivesCurrent treatment guidelines for patients with isocitrate dehydrogenase (IDH)-mutant (IDHm) glioma recommend radiation (XRT) and chemotherapy after surgery in most cases based on studies in which XRT was compared with XRT plus chemotherapy. Although XRT has been shown to improve time to tumor progression, there has never been a controlled study in this population in which adjuvant XRT (aXRT) demonstrated superior overall survival (OS) over initial observation. The aim of this study was to evaluate the effect of timing of XRT on survival in IDHm-glioma.
methodsWe performed a retrospective observational cohort study, comprising a cohort of adult patients with grade 2 or 3 IDHm-gliomas seen at 2 academic centers (University of Washington and Stanford University) between 2007 and 2022 (identified through research data registries). The main comparison of interest was patients who received XRT within 3 months of diagnosis and before progression, that is, as adjuvant treatment (aXRT), versus those who did not have aXRT (deferred XRT, dXRT). The primary outcome measures were median progression-free survival and OS. Survival analysis was performed through multivariable Cox proportional hazard modeling, propensity matching, and subset analysis.
resultsA total of 450 eligible patients were identified (mean age 39.7 years; 41% female). The median survival of the combined cohort was 19.1 years (25th-75th percentiles 9.75-27.8 years). 47.1% of patients received aXRT. Patients with aXRT demonstrated similar time to next intervention (hazard ratio [HR] 0.83, 95% CI 0.65-1.07) but showed a markedly diminished OS compared with the dXRT cohort (HR of death 2.90, 95% CI 1.9-4.42, DISCUSSION: Although retrospective, the marked OS difference between aXRT and dXRT groups suggests that aXRT may be not be as beneficial as what was once thought, especially regarding long-term survival. These results also offer justification for the use of a dXRT group in studies assessing adjuvant treatments, as well as a reconsideration of the current treatment paradigm for these patients, especially given the recent introduction of IDH inhibitors.
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