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脊髓星形细胞瘤的治疗、预后因素和结果。

Treatment, prognostic factors, and outcomes in spinal cord astrocytomas.

机构信息

Baylor College of Medicine, Waco, Texas, USA.

出版信息

Neuro Oncol. 2013 Apr;15(4):406-12. doi: 10.1093/neuonc/nos309. Epub 2013 Jan 14.

Abstract

BACKGROUND

Spinal astrocytomas are rare intramedullary CNS tumors for which there is limited consensus on treatment; the importance of the extent of resection (EOR), postoperative radiotherapy, and chemotherapy remains poorly understood. We report on outcomes associated with surgery, postoperative radiotherapy, and chemotherapy in a series of patients treated at M. D. Anderson Cancer Center (MDACC) with the aim of elucidating the role of these treatments in spinal astrocytomas.

METHODS

We retrospectively reviewed charts from a series of 83 patients with histologically confirmed spinal astrocytoma treated at MDACC during 1990-2011. Data collected included patient demographic characteristics, prognostic indicators, and treatment modality at diagnosis. We analyzed overall survival (OS) and progression-free survival (PFS) for pilocytic (World Health Organization [WHO] grade I) and infiltrative (WHO grades II, III, and IV) astrocytomas, separately. Multivariate analysis was performed for the infiltrative patients but not the pilocytic patients because of a limited number of cases.

RESULTS

Higher WHO grade among all patients was associated with worse OS (P < .0001) and PFS (P = .0003). Among patients with infiltrative tumors, neither EOR nor radiotherapy was associated with a difference in outcomes in multivariate analysis; however, among patients with infiltrative astrocytomas, chemotherapy was significantly associated with improved PFS (hazard ratio = .22, P = .0075) but not OS (hazard ratio = .89, P = .83) in multivariate analysis.

CONCLUSION

WHO grade was the strongest prognostic indicator in patients with spinal cord astrocytomas. Our results also show that chemotherapy improved PFS in infiltrative astrocytomas in multivariate analysis, but neither EOR nor radiation therapy influenced outcomes in this group.

摘要

背景

脊髓星形细胞瘤是一种罕见的髓内中枢神经系统肿瘤,对于其治疗方法尚未达成广泛共识;手术切除范围(EOR)、术后放疗和化疗的重要性仍知之甚少。我们报告了在 M.D.安德森癌症中心(MDACC)治疗的一系列患者中与手术、术后放疗和化疗相关的结果,旨在阐明这些治疗方法在脊髓星形细胞瘤中的作用。

方法

我们回顾性分析了 1990 年至 2011 年期间在 MDACC 接受治疗的 83 例组织学证实的脊髓星形细胞瘤患者的病历。收集的数据包括患者的人口统计学特征、预后指标和诊断时的治疗方式。我们分别分析了毛细胞型星形细胞瘤(世界卫生组织[WHO] 1 级)和浸润性星形细胞瘤(WHO 2、3 和 4 级)的总生存率(OS)和无进展生存率(PFS)。由于浸润性患者的病例数有限,因此仅对浸润性患者进行了多变量分析,而未对毛细胞型患者进行分析。

结果

所有患者的 WHO 分级越高,OS(P <.0001)和 PFS(P =.0003)越差。在浸润性肿瘤患者中,EOR 和放疗均与多变量分析中的结局无差异;然而,在浸润性星形细胞瘤患者中,化疗与改善的 PFS 显著相关(风险比=0.22,P =0.0075),但与 OS 无关(风险比=0.89,P =0.83)。

结论

在脊髓星形细胞瘤患者中,WHO 分级是最强的预后指标。我们的结果还表明,化疗在多变量分析中改善了浸润性星形细胞瘤的 PFS,但 EOR 和放疗均未影响该组患者的结局。

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