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1p19q共缺失/部分缺失型胶质瘤的治疗结果

Treatment Outcomes in 1p19q Co-deleted/Partially Deleted Gliomas.

作者信息

McNamara Mairéad G, Jiang Haiyan, Lim-Fat Mary Jane, Sahebjam Solmaz, Kiehl Tim-Rasmus, Karamchandani Jason, Coire Claire, Chung Caroline, Millar Barbara-Ann, Laperriere Normand, Mason Warren P

机构信息

1Department of Medical Oncology,Princess Margaret Cancer Centre,Toronto,Canada.

3Department of Biostatistics,Princess Margaret Cancer Centre,Toronto,Canada.

出版信息

Can J Neurol Sci. 2017 May;44(3):288-294. doi: 10.1017/cjn.2016.420.

Abstract

BACKGROUND

Radiotherapy with procarbazine, lomustine, and vincristine improves overall survival (OS) in patients with 1p19q co-deleted anaplastic oligodendroglioma/anaplastic oligoastrocytoma.

METHODS

This retrospective analysis investigated outcomes in patients with 1p19q co-deleted/partially deleted oligodendroglioma, oligoastrocytoma, anaplastic oligodendroglioma, or anaplastic oligoastrocytoma. OS and progression-free survival (PFS) were analyzed using the Kaplan-Meier method and prognostic factors using the Cox proportional hazard model.

RESULTS

A total of 106 patients (between December 1997 and December 2013) were included. Median age was 40 years (19-66), 58 were male (55%), Eastern Cooperative Oncology Group performance status was 0 in 80 patients (75%). 1p19q status was co-deleted in 66 (62%), incompletely co-deleted in 27 (25%), and 1p or 19q loss alone in four (4%) and nine (8%) patients, respectively. Isocitrate dehydrogenase-1 R132H mutation was found in 67 of 85 patients with sufficient material. Upfront treatment was given in 72 (68%) patients and temozolomide alone in 52 (49%). Median time to radiotherapy in 47 patients (44%) was 34.7 months and 41.2 months in 9 patients with co-deleted/incompletely co-deleted anaplastic oligodendroglioma/anaplastic oligoastrocytoma who received upfront temozolomide alone. Median OS was not reached and 5-year OS was 91% for all groups (median follow-up, 5.1 years). On multivariable analysis for all patients, receipt of therapy upfront versus none (p=0.04), PS 1 versus 0 (p<0.001) and 1p19q co-deletion/incomplete deletion versus 1p or 19q loss alone (p=0.005) were prognostic for PFS. Isocitrate dehydrogenase-1 status was not prognostic for PFS.

CONCLUSIONS

With similar survival patterns in low-grade/anaplastic gliomas, molecular characteristics may be more important than histological grade. Longer follow-up and results of prospective trials are needed for definitive guidance on treatment of these patients.

摘要

背景

对于1p19q共缺失的间变性少突胶质细胞瘤/间变性少突星形细胞瘤患者,采用丙卡巴肼、洛莫司汀和长春新碱进行放疗可改善总生存期(OS)。

方法

这项回顾性分析调查了1p19q共缺失/部分缺失的少突胶质细胞瘤、少突星形细胞瘤、间变性少突胶质细胞瘤或间变性少突星形细胞瘤患者的预后。采用Kaplan-Meier方法分析总生存期(OS)和无进展生存期(PFS),并使用Cox比例风险模型分析预后因素。

结果

共纳入106例患者(1997年12月至2013年12月)。中位年龄为40岁(19 - 66岁),58例为男性(55%),东部肿瘤协作组体能状态评分为0分的患者有80例(75%)。66例(62%)患者1p19q状态共缺失,27例(25%)患者为不完全共缺失,4例(4%)和9例(8%)患者分别仅存在1p或19q缺失。在85例有足够样本的患者中,67例检测到异柠檬酸脱氢酶-1 R132H突变。72例(68%)患者接受了初始治疗,52例(49%)患者仅接受替莫唑胺治疗。47例(44%)患者放疗的中位时间为34.7个月,9例仅接受初始替莫唑胺治疗的共缺失/不完全共缺失间变性少突胶质细胞瘤/间变性少突星形细胞瘤患者放疗的中位时间为41.2个月。所有组的中位总生存期未达到,5年总生存率为91%(中位随访时间为5.1年)。对所有患者进行多变量分析时,接受初始治疗与未接受治疗(p = 0.04)、体能状态评分为1分与0分(p < 0.001)以及1p19q共缺失/不完全缺失与仅1p或19q缺失(p = 0.005)对无进展生存期有预后意义。异柠檬酸脱氢酶-1状态对无进展生存期无预后意义。

结论

在低级别/间变性胶质瘤中生存模式相似,分子特征可能比组织学分级更重要。需要更长时间的随访和前瞻性试验结果来为这些患者的治疗提供明确指导。

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