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液体活检指导不可切除的小儿脑干肿瘤的成功分子靶向治疗。

Liquid biopsy guides successful molecular targeted therapy of an inoperable pediatric brainstem neoplasm.

作者信息

Arthur Cecilia, Carlson Lena-Maria, Svoboda Jan, Sandvik Ulrika, Jylhä Cecilia, Nordenskjöld Magnus, Holm Stefan, Tham Emma

机构信息

Clinical Genetics, Karolinska University Hospital, 171 76, Stockholm, Sweden.

Department of Molecular Medicine and Surgery, Karolinska Institutet, 171 76, Stockholm, Sweden.

出版信息

NPJ Precis Oncol. 2024 Feb 22;8(1):44. doi: 10.1038/s41698-024-00535-8.

Abstract

Midline CNS tumors are occasionally inaccessible for surgical biopsies. In these instances, cell-free DNA (cfDNA) may serve as a viable alternative for molecular analysis and identification of targetable mutations. Here, we report a young child with an inoperable brainstem tumor in whom a stereotactic biopsy was deemed unsafe. The tumor progressed on steroids and after radiotherapy the patient developed hydrocephalus and received a ventriculoperitoneal shunt. Droplet digital PCR analysis of cfDNA from an intraoperative cerebrospinal fluid liquid biopsy revealed a BRAF V600 mutation enabling targeted treatment with MEK and BRAF inhibitors. The patient, now on trametinib and dabrafenib for 1 year, has had substantial tumor volume regression and reduction of contrast enhancement on MRIs and is making remarkable clinical progress. This case highlights that in a subset of CNS tumors, access to liquid biopsy analysis may be crucial to identify actionable therapeutic targets that would otherwise go undiscovered.

摘要

中线中枢神经系统肿瘤有时无法进行手术活检。在这些情况下,游离DNA(cfDNA)可作为分子分析和鉴定可靶向突变的可行替代方法。在此,我们报告一名患有无法手术的脑干肿瘤的幼儿,立体定向活检被认为不安全。肿瘤在类固醇治疗下进展,放疗后患者出现脑积水并接受了脑室腹腔分流术。对术中脑脊液液体活检的cfDNA进行液滴数字PCR分析,发现了BRAF V600突变,从而能够用MEK和BRAF抑制剂进行靶向治疗。该患者目前服用曲美替尼和达拉非尼已1年,肿瘤体积显著缩小,MRI上的对比增强减少,临床进展显著。该病例突出表明,在一部分中枢神经系统肿瘤中,进行液体活检分析对于识别否则将无法发现的可采取行动的治疗靶点可能至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/87b7/10884019/7645b3bb73c9/41698_2024_535_Fig1_HTML.jpg

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