预测胶质母细胞瘤中BRAF V600E突变:影像学特征的应用

IF 2.7 3区 医学 Q2 CLINICAL NEUROLOGY Brain Tumor Pathology Pub Date : 2021-07-01 Epub Date: 2021-07-03 DOI:10.1007/s10014-021-00407-0
Manabu Natsumeda, Michael Chang, Ramil Gabdulkhaev, Haruhiko Takahashi, Yoshihiro Tsukamoto, Yu Kanemaru, Masayasu Okada, Makoto Oishi, Kouichirou Okamoto, Fausto J Rodriguez, Akiyoshi Kakita, Yukihiko Fujii, Karisa C Schreck
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引用次数: 7

摘要

在胶质母细胞瘤(GBMs)中检测BRAF V600E突变非常重要,因为它具有潜在的治疗意义。尽管如此,这些突变的相对稀少使得对所有GBMs的分子检测存在争议。在本研究中,我们分析了来自2个机构的12例BRAF v600e突变GBMs和12例匹配对照的临床、影像学和病理特征。我们发现,大多数BRAF v600e突变型GBMs在MRI上表现为边界清晰的病变、薄壁大囊性成分和实心皮质成分的组合,但与匹配的BRAF野生型对照有一些重叠(p = 0.069)。BRAF v600e突变型GBMs也倾向于大体全切除(83%对17%,p = 0.016),形态学上显示上皮样特征(83%对0%,p = 0.016)
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Predicting BRAF V600E mutation in glioblastoma: utility of radiographic features.

Detection of BRAF V600E mutation in glioblastomas (GBMs) is important because of potential therapeutic implications. Still, the relative paucity of these mutations makes molecular detection in all GBMs controversial. In the present study, we analyzed clinical, radiographic and pathologic features of 12 BRAF V600E-mutant GBMs and 12 matched controls from 2 institutions. We found that a majority of BRAF V600E-mutant GBMs displayed a combination of well-circumscribed lesions, large cystic components with thin walls and solid cortical component on MRI, but with some overlap with matched BRAF wildtype controls (p = 0.069). BRAF V600E-mutant GBMs were also apt to gross total resection (83% vs 17%, p = 0.016) and morphologically displayed epithelioid features (83% vs 0%, p < 0.0001). Identification of these clinical, radiographic, and pathologic characteristics should prompt testing for BRAF V600E in IDH-wildtype GBM.

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来源期刊
Brain Tumor Pathology
Brain Tumor Pathology 医学-病理学
CiteScore
5.40
自引率
9.10%
发文量
30
审稿时长
>12 weeks
期刊介绍: Brain Tumor Pathology is the official journal of the Japan Society of Brain Tumor Pathology. This international journal documents the latest research and topical debate in all clinical and experimental fields relating to brain tumors, especially brain tumor pathology. The journal has been published since 1983 and has been recognized worldwide as a unique journal of high quality. The journal welcomes the submission of manuscripts from any country. Membership in the society is not a prerequisite for submission. The journal publishes original articles, case reports, rapid short communications, instructional lectures, review articles, letters to the editor, and topics.Review articles and Topics may be recommended at the annual meeting of the Japan Society of Brain Tumor Pathology. All contributions should be aimed at promoting international scientific collaboration.
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