Abstract

The aim of this study was to evaluate prognostic factors including surgical, radiographic, and histopathologic analyses in anaplastic oligodendroglioma (AO) patients. We reviewed the electronic records of 95 patients who underwent surgery and were diagnosed with AO for 20 years. The primary endpoints were progression-free survival (PFS) and overall survival (OS). Univariate and multivariable analyses included clinical, histopathological, and radiographic prognostic factors. Subgroup analysis was performed in isocitrate dehydrogenase (IDH1/2)-mutant and 1p/19q-codeleted patients. The median PFS and OS were 24.7 months and 50.8 months, respectively. The 1-, 3-, 5-, and 10-year PFS were 75.8%, 42.9%, 32.4%, and 16.4%, respectively. Furthermore, the 1-, 3-, 5-, and 10-year OS were 98.9%, 76.9%, 42.9%, and 29.7%, respectively. The median PFS and OS of the IDH1/2-mutant and 1p/19q-codeleted patients were 54.2 and 57.8 months, respectively. In univariate analyses, young age, frontal lobe, weak enhancement, gross total resection (GTR), low Ki-67 index, 1p/19q codeletion, and IDH1/2 mutations were associated with a favorable outcome. In multivariable analyses, IDH1/2 mutation was related to better PFS and OS. In subgroup analysis, GTR was associated with favorable outcomes.

Highlights

  • The aim of this study was to evaluate prognostic factors including surgical, radiographic, and histopathologic analyses in anaplastic oligodendroglioma (AO) patients

  • Mutations in the isocitrate dehydrogenase genes (IDH1/2) and chromosome 1p/19q codeletion status are key in defining oligodendroglioma

  • We reviewed the electronic records of patients who underwent surgical procedures at our institute and were diagnosed with AO from January 1998 to December 2018

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Summary

Introduction

The aim of this study was to evaluate prognostic factors including surgical, radiographic, and histopathologic analyses in anaplastic oligodendroglioma (AO) patients. The median PFS and OS of the IDH1/2-mutant and 1p/19q-codeleted patients were 54.2 and 57.8 months, respectively. Kang et al published a multicenter study of AO which included 376 patients from nine Korean institutes They reported that 5-year and 10-year survival rate of AO was 58% and 45%, respectively. The median PFS was 34.5 months, and the actuarial 5- and 10-years PFS rates were 38% and 24%, ­respectively[7] The limitation of those studies was histological diagnosis, not molecular diagnosis. Our study tries to overcome this limitation by subgroup analysis which included molecular diagnosis as IDH1/2-mutant and 1p/19q codeleted AO. According to these results, we performed a subgroup analysis in IDH1/2-mutant and 1p/19q-codeleted AO patients to predict their prognosis

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