IDH-Mutant Astrocytomas in Patients Older than 55 Years: A Retrospective Analysis.

IF 0.9 4区 医学 Q4 PATHOLOGY
Rasha Alfattal, Keng Lam, Hanim I Ozkizilkaya, Chirag B Patel, Daniel H Wang, Jason T Huse, Leomar Y Ballester, Maria A Gubbiotti
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Abstract

Diffuse gliomas are the most common malignant brain tumors in adults, stratified by isocitrate dehydrogenase (IDH1/IDH2) mutation status. While the median age for central nervous system (CNS) World Health Organization (WHO) grade 2 to 3 IDH-mutant astrocytomas is 38 years, older patients of >55 years predominantly exhibit IDH-wildtype gliomas and confer a poorer prognosis. To examine the clinicopathologic spectrum of IDH-mutant astrocytomas in older adults, we retrospectively reviewed all astrocytic tumors diagnosed at our institution between 2021 and 2024 in patients >55 years. Twenty-two IDH-mutant astrocytomas (median age: 63 years; range: 56-79; male:female = 9:13) were identified and compared descriptively to a historical cohort of 179 IDH-mutant astrocytomas in younger patients. Grade distribution among older patients paralleled that of younger adults: CNS WHO grade 2 (55%), grade 3 (18%), and grade 4 (27%). Magnetic resonance imaging (MRI) showed T2/FLAIR mismatch sign in 25% of grade 2 tumors and in none of the higher grades; 50% of grade 2 tumors demonstrated contrast enhancement. IDH1 p.R132H accounted for 95% of mutations, with 1 p.R132G variant. ATRX loss was seen in 71% and strong p53 immunoreactivity in 83% of evaluable tumors. Copy-number analysis (n = 10) revealed CDKN2A/B homozygous deletion in 10% and heterozygous loss in 20%. Despite their rarity, IDH-mutant astrocytomas in older adults are more prevalent than historically appreciated and maintain imaging and molecular profiles akin to tumors in younger adults. Accordingly, IDH1 p.R132H-specific immunohistochemistry remains a cost-effective first-line screening tool irrespective of age.

55岁以上患者的idh突变星形细胞瘤:回顾性分析
弥漫性胶质瘤是成人中最常见的恶性脑肿瘤,根据异柠檬酸脱氢酶(IDH1/IDH2)突变状态分层。虽然中枢神经系统(CNS)世界卫生组织(WHO) 2 - 3级idh突变星形细胞瘤的中位年龄为38岁,但年龄在bb0 - 55岁的老年患者主要表现为idh野生型胶质瘤,预后较差。为了研究老年人idh突变型星形细胞瘤的临床病理谱,我们回顾性分析了我院在2021年至2024年间诊断出的所有年龄在55岁至55岁之间的星形细胞瘤。鉴定出22例idh突变星形细胞瘤(中位年龄:63岁;范围:56-79岁;男性:女性= 9:13),并与179例年轻患者idh突变星形细胞瘤的历史队列进行描述性比较。老年患者的分级分布与年轻人相似:CNS WHO 2级(55%)、3级(18%)和4级(27%)。磁共振成像(MRI)显示T2/FLAIR不匹配征象在25%的2级肿瘤中,没有更高级别的肿瘤;50%的2级肿瘤显示对比增强。IDH1 p.R132H占95%的突变,其中p.R132G变异1个。在可评估的肿瘤中,ATRX缺失占71%,p53免疫反应性强占83%。拷贝数分析(n = 10)显示CDKN2A/B纯合缺失占10%,杂合缺失占20%。尽管罕见,但idh突变型星形细胞瘤在老年人中比以往认为的更为普遍,并保持与年轻人肿瘤相似的影像学和分子特征。因此,IDH1 p.r 132h特异性免疫组织化学仍然是一种具有成本效益的一线筛查工具,与年龄无关。
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来源期刊
CiteScore
2.10
自引率
0.00%
发文量
198
审稿时长
1 months
期刊介绍: International Journal of Surgical Pathology (IJSP) is a peer-reviewed journal published eight times a year, which offers original research and observations covering all major organ systems, timely reviews of new techniques and procedures, discussions of controversies in surgical pathology, case reports, and images in pathology. This journal is a member of the Committee on Publication Ethics (COPE).
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