Abstract

Anaplastic oligodendroglioma is a rare disease with an inadequately understood prognosis. The aim of this study was to investigate factors associated with survival outcome in anaplastic oligodendroglioma patients. A population-based cohort study was conducted based on the Surveillance, Epidemiology, and End Results program. In total, 1899 patients with a histological diagnosis of anaplastic oligodendroglioma from 1973 to 2015 were included. Mean age at diagnosis was 49.2 years, and 56.19% were male. In our study, 62.40% of patients were married, and 87.05% were white. Most patients (90.42%) were diagnosed with anaplastic oligodendroglioma as their first malignant primary tumor, but 9.58% had a diagnosis of at least one other primary malignancy; 87.89% of patients had received cancer-directed surgery. Patients receiving surgery had a better prognosis for overall survival compared to those not receiving surgery after propensity score matching analysis (p<0.05). The overall 1-, 3-, 5-, and 10-year survival of anaplastic oligodendroglioma was 78.7%, 60%, 50.2%, and 36.2%, respectively. Kaplan-Meier analysis indicated that age, marital status, presence of multiple primary malignancies, and surgical treatment were associated with overall survival, whereas sex and race were not. Moreover, age at diagnosis of 52 years was calculated as an optimal cutoff value to distinguish better and worse overall survival. Multivariate Cox proportional hazard analysis indicated that older age (OR 1.040, 95%CI1.035–1.045), single patients (OR 1.293, 95%CI 1.103–1.515), and presence of multiple primary malignancies (OR 1.501, 95%CI 1.238–1.820) were significantly associated with worse overall survival, whereas surgery (OR 0.584, 95%CI 0.494–0.689) was associated with better overall survival. A nomogram predicting 5-, and 10-year survival probability for anaplastic oligodendroglioma was constructed based on these variables. In conclusion, age, marital status, presence of multiple primary malignancies, and surgical treatment were associated with survival of anaplastic oligodendroglioma.

Highlights

  • The aim of this study was to investigate factors associated with survival outcome in anaplastic oligodendroglioma patients

  • Primary central nervous system (CNS) tumors are a diverse group of neoplasms arising from a wide range of CNS cells

  • From 1973 to 2015, 1989 patients were diagnosed with AO

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Summary

Introduction

Primary central nervous system (CNS) tumors are a diverse group of neoplasms arising from a wide range of CNS cells. Prognostic factors for anaplastic oligodendroglioma all primary CNS tumors and 4% to 15% of gliomas.[2] Oligodendrogliomas are tumors of oligodendrocytes and often occur in patients aged 40 to 60 years, with an average age at diagnosis of approximately 45 years.[3,4] The World Health Organization (WHO) has divided oligodendroglioma into low-grade well-differentiated oligodendroglioma (WHO grade II) and anaplastic astrocytoma (AO) (WHO grade III).[4]

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