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成人 IDH 突变型脑桥胶质瘤的临床转归、影像学表现和遗传学特征。

Clinical outcome, radiological findings, and genetic features of IDH-mutant brainstem glioma in adults.

机构信息

Department of Neurosurgery, Hokkaido University Graduate School of Medicine, Kita 15 Nishi 7, Kita-Ku, Sapporo, Hokkaido, Japan.

Department of Cancer Pathology, Hokkaido University Graduate School of Medicine, Sapporo, Japan.

出版信息

Acta Neurochir (Wien). 2024 Jun 12;166(1):263. doi: 10.1007/s00701-024-06154-3.

Abstract

BACKGROUND

With the recent advent of genetic testing, IDH-mutant glioma has been found among adult brainstem gliomas. However, the clinical outcome and prognosis of IDH-mutant brainstem gliomas in adults have not been elucidated. This study aimed to investigate the clinical outcome, radiological findings, and genetic features of adult patients with IDH-mutant diffuse brainstem gliomas.

METHODS

Data from adult patients with brainstem glioma at Hokkaido University Hospital between 2006 and 2022 were retrospectively analyzed. Patient characteristics, treatment methods, genetic features, and prognosis were evaluated.

RESULTS

Of 12 patients with brainstem glioma with proven histopathology, 4 were identified with IDH mutation. All patients underwent local radiotherapy with 54 Gray in 27 fractions combined with chemotherapy with temozolomide. Three patients had IDH1 R132H mutation and one had IDH2 R172G mutation. The median progression-free survival and overall survival were 68.4 months and 85.2 months, respectively, longer than that for IDH-wildtype gliomas (5.6 months and 12.0 months, respectively). At the time of initial onset, contrast-enhanced lesions were observed in two of the four cases in magnetic resonance imaging.

CONCLUSION

As some adult brainstem gliomas have IDH mutations, and a clearly different prognosis from those with IDH-wildtype, biopsies are proactively considered to confirm the genotype.

摘要

背景

随着基因检测的出现,成人脑干胶质瘤中发现了 IDH 突变型。然而,成人 IDH 突变型脑干胶质瘤的临床结果和预后尚未阐明。本研究旨在探讨成人 IDH 突变型弥漫性脑干胶质瘤的临床结果、影像学表现和遗传特征。

方法

回顾性分析了北海道大学医院 2006 年至 2022 年期间的成人脑干胶质瘤患者数据。评估了患者特征、治疗方法、遗传特征和预后。

结果

在经组织病理学证实的 12 例脑干胶质瘤患者中,有 4 例存在 IDH 突变。所有患者均接受局部放疗(54 Gray,27 次分割)联合替莫唑胺化疗。3 例 IDH1 R132H 突变,1 例 IDH2 R172G 突变。中位无进展生存期和总生存期分别为 68.4 个月和 85.2 个月,均长于 IDH 野生型胶质瘤(分别为 5.6 个月和 12.0 个月)。在初始发病时,4 例中有 2 例磁共振成像显示对比增强病变。

结论

由于一些成人脑干胶质瘤存在 IDH 突变,其预后与 IDH 野生型明显不同,因此积极考虑进行活检以确定基因型。

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