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解析 IDH 突变型星形细胞瘤 4 级患者的预后特征:一项大型多中心回顾性研究。

Dissecting the prognostic signature of patients with astrocytoma isocitrate dehydrogenase-mutant grade 4: a large multicenter, retrospective study.

机构信息

Medical Oncology and Hematology Unit, IRCCS Humanitas Research Hospital, Rozzano, Milan. Electronic address: https://twitter.com/AngeloDipa_.

Nervous System Medical Oncology Department, IRCCS Istituto delle Scienze Neurologiche di Bologna, Bologna.

出版信息

ESMO Open. 2024 Jun;9(6):103485. doi: 10.1016/j.esmoop.2024.103485. Epub 2024 Jun 3.

Abstract

BACKGROUND

The World Health Organization (WHO) 2021 classification of central nervous system (CNS) tumors classified astrocytoma isocitrate dehydrogenase-mutant (A IDHm) with either microvascular proliferation and/or necrosis or homozygous deletion of CDKN2A/B as CNS grade 4 (CNS WHO G4), introducing a distinct entity and posing new challenges to physicians for appropriate management and prognostication.

PATIENTS AND METHODS

We retrospectively collected information about patients diagnosed with A IDHm CNS WHO G4 at three reference neuro-oncological Italian centers and correlated them with survival.

RESULTS

A total of 133 patients were included. Patients were young (median age 41 years) and most received post-operative treatment including chemo-radiation (n = 101) and/or temozolomide maintenance (n = 112). With a median follow-up of 51 months, the median overall survival (mOS) was 31.2 months, with a 5-year survival probability of 26%. In the univariate analysis, complete resection (mOS: 40.2 versus 26.3 months, P = 0.03), methyl-guaninemethyltransferase (MGMT) promoter methylation (mOS: 40.7 versus 18 months, P = 0.0136), and absence of telomerase reverse transcriptase (TERT) promoter mutation (mOS: 40.7 versus 18 months, P = 0.0003) correlated with better prognosis. In the multivariate models, lack of TERT promoter mutation [hazard ratio (HR) 0.23, 95% confidence interval (CI) 0.07-0.82, P = 0.024] and MGMT methylation (HR 0.40, 95% CI 0.20-0.81, P = 0.01) remained associated with improved survival.

CONCLUSIONS

This is the largest experience in Western countries exploring the prognostic signature of patients with A IDHm CNS G4. Our results show that MGMT promoter methylation and TERT promoter mutation may impact clinical outcomes. This may support physicians in prognostication, clinical management, and design of future studies of this distinct diagnostic entity.

摘要

背景

世界卫生组织(WHO)2021 年中枢神经系统(CNS)肿瘤分类将伴微血管增生和/或坏死或 CDKN2A/B 纯合缺失的星形细胞瘤 IDH 突变型(A IDHm)归类为 CNS 分级 4(CNS WHO G4),这引入了一个独特的实体,并给医生在适当的管理和预后方面带来了新的挑战。

患者和方法

我们回顾性收集了在意大利三个参考神经肿瘤学中心诊断为 A IDHm CNS WHO G4 的患者的信息,并与生存情况进行了相关性分析。

结果

共纳入 133 例患者。患者年龄较轻(中位年龄 41 岁),大多数患者接受了术后治疗,包括放化疗(n=101)和/或替莫唑胺维持治疗(n=112)。中位随访 51 个月时,中位总生存期(mOS)为 31.2 个月,5 年生存率为 26%。在单因素分析中,完全切除(mOS:40.2 与 26.3 个月,P=0.03)、甲基鸟嘌呤甲基转移酶(MGMT)启动子甲基化(mOS:40.7 与 18 个月,P=0.0136)和端粒酶逆转录酶(TERT)启动子突变缺失(mOS:40.7 与 18 个月,P=0.0003)与更好的预后相关。在多因素模型中,缺乏 TERT 启动子突变[风险比(HR)0.23,95%置信区间(CI)0.07-0.82,P=0.024]和 MGMT 甲基化(HR 0.40,95%CI 0.20-0.81,P=0.01)仍然与生存改善相关。

结论

这是西方国家在探索 A IDHm CNS G4 患者预后特征方面最大的经验。我们的结果表明,MGMT 启动子甲基化和 TERT 启动子突变可能影响临床结局。这可能有助于医生进行预后、临床管理和这一独特诊断实体的未来研究设计。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/65bd/11179079/8eae41beae42/gr1.jpg

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