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少突胶质细胞瘤切除术:监测、流行病学和最终结果(SEER)分析。

Oligodendroglioma resection: a Surveillance, Epidemiology, and End Results (SEER) analysis.

机构信息

1School of Medicine, and.

2Division of Neurological Surgery, University of California, San Diego, California; and.

出版信息

J Neurosurg. 2018 Apr;128(4):1076-1083. doi: 10.3171/2016.11.JNS161974. Epub 2017 May 12.

Abstract

OBJECTIVE The available evidence suggests that the clinical benefits of extended resection are limited for chemosensitive tumors, such as primary CNS lymphoma. Oligodendroglioma is generally believed to be more sensitive to chemotherapy than astrocytoma of comparable grades. In this study the authors compare the survival benefit of gross-total resection (GTR) in patients with oligodendroglioma relative to patients with astrocytoma. METHODS Using the Surveillance, Epidemiology, and End Results (SEER) Program (1999-2010) database, the authors identified 2378 patients with WHO Grade II oligodendroglioma (O2 group) and 1028 patients with WHO Grade III oligodendroglioma (O3 group). Resection was defined as GTR, subtotal resection, biopsy only, or no resection. Kaplan-Meier and multivariate Cox regression survival analyses were used to assess survival with respect to extent of resection. RESULTS Cox multivariate analysis revealed that the hazard of dying from O2 and O3 was comparable between patients who underwent biopsy only and GTR (O2: hazard ratio [HR] 1.06, 95% confidence interval [CI] 0.73-1.53; O3: HR 1.18, 95% CI 0.80-1.72). A comprehensive search of the published literature identified 8 articles without compelling evidence that GTR is associated with improved overall survival in patients with oligodendroglioma. CONCLUSIONS This SEER-based analysis and review of the literature suggest that GTR is not associated with improved survival in patients with oligodendroglioma. This finding contrasts with the documented association between GTR and overall survival in anaplastic astrocytoma and glioblastoma. The authors suggest that this difference may reflect the sensitivity of oligodendroglioma to chemotherapy as compared with astrocytomas.

摘要

目的

现有证据表明,对于化疗敏感的肿瘤(如原发性中枢神经系统淋巴瘤),扩大切除术的临床获益有限。少突胶质细胞瘤通常被认为比同等分级的星形细胞瘤对化疗更敏感。在这项研究中,作者比较了全切除(GTR)在少突胶质细胞瘤患者中的生存获益,与星形细胞瘤患者进行了比较。

方法

作者利用监测、流行病学和最终结果(SEER)计划(1999-2010 年)数据库,确定了 2378 例世界卫生组织(WHO)分级 II 级少突胶质细胞瘤(O2 组)和 1028 例 WHO 分级 III 级少突胶质细胞瘤(O3 组)患者。切除术定义为 GTR、次全切除术、活检或未行切除术。Kaplan-Meier 和多变量 Cox 回归生存分析用于评估与切除范围相关的生存情况。

结果

Cox 多变量分析显示,仅行活检和 GTR 的患者的 O2 和 O3 死亡风险相当(O2:危险比[HR]1.06,95%置信区间[CI]0.73-1.53;O3:HR 1.18,95%CI 0.80-1.72)。对已发表文献的全面检索未发现有力证据表明 GTR 与少突胶质细胞瘤患者的总生存改善相关。

结论

这项基于 SEER 的分析和文献复习表明,GTR 与少突胶质细胞瘤患者的生存改善无关。这一发现与间变性星形细胞瘤和胶质母细胞瘤中 GTR 与总生存之间的关联形成对比。作者认为,这种差异可能反映了少突胶质细胞瘤与星形细胞瘤相比对化疗的敏感性。

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