論文ID: 2025-0366
Oligodendrogliomas generally have a better prognosis than other adult-type diffuse gliomas. However, although several clinical and radiological prognostic factors have been reported, long-term outcomes remain heterogeneous, and decisions regarding postoperative treatment remain challenging because of concerns about long-term adverse effects. This study aimed to explore prognostic factors by analyzing clinical, radiological, therapeutic, and genetic data from a single-institution cohort.
We retrospectively reviewed adult patients (≥18 years) with isocitrate dehydrogenase-mutant and 1p/19q-codeleted oligodendrogliomas who underwent surgical resection at our institution between 1999 and 2021, with available preoperative magnetic resonance imaging and computed tomography. CDKN2A/B copy number status was assessed using multiplex ligation-dependent probe amplification and confirmed by fluorescence in situ hybridization. Overall survival and progression-free survival were analyzed using the Kaplan-Meier method and Cox proportional hazards models. For overall survival, simple multivariable Cox models adjusted for age and Karnofsky Performance Status were constructed.
A total of 32 patients were included. The median age was 40 years, and the median Karnofsky Performance Status was 90. Calcification and corpus callosum invasion were observed in 46.9% and 40.6% of cases, respectively, and CDKN2A/B hemizygous deletion was identified in four cases. The 5-year progression-free survival was 62.0%, and the 5-year overall survival was 86.5%. On univariable Cox analysis for overall survival, corpus callosum invasion, calcification, and CDKN2A/B hemizygous deletion were significant adverse prognostic factors. In simple multivariable Cox models, CDKN2A/B hemizygous deletion remained associated with shorter overall survival.
Calcification, corpus callosum invasion, and CDKN2A/B hemizygous deletion may be prognostic markers in oligodendroglioma.
