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将体细胞panel 纳入检测具有白血病倾向综合征和获得性血细胞减少症的儿童和青年患者的造血转化。

Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias.

机构信息

Pediatric Hematology Laboratory, Felsenstein Medical Research Center, Petach Tikva, Israel.

Department of Hematology-Oncology, Schneider Children's Medical Center of Israel, Petach Tikva, Israel.

出版信息

Br J Haematol. 2021 May;193(3):570-580. doi: 10.1111/bjh.17285. Epub 2020 Dec 27.

Abstract

Detection of somatic mutations may help verify the diagnosis of myelodysplastic syndrome (MDS) in patients with persistent cytopenias or with MDS-predisposition syndromes, prior to the development of overt leukemia. However, the spectrum and consequences of acquired changes in paediatric patients have not been fully evaluated, and especially not in the context of an underlying syndrome. We incorporated a targeted next-generation-sequencing panel of 54 genes for the detection of somatic mutations in paediatric and young adult patients with inherited or acquired cytopenias. Sixty-five patients were included in this study, of whom 17 (26%) had somatic mutations. We detected somatic mutations in 20% of individuals with inherited MDS-predisposition syndromes, including in patients with severe congenital neutropenia and Fanconi anaemia, and with germline mutations in SAMD9L. Thirty-eight per cent of children with acquired cytopenias and suspected MDS had somatic changes, most commonly in genes related to signal transduction and transcription. Molecularly abnormal clones often preceded cytogenetic changes. Thus, routine performance of somatic panels can establish the diagnosis of MDS and determine the optimal timing of haematopoietic stem cell transplantation, prior to the development of leukaemia. In addition, performing somatic panels in patients with inherited MDS-predisposition syndromes may reveal their unique spectrum of acquired mutations.

摘要

检测体细胞突变有助于在明显白血病发生之前,对持续性血细胞减少症或 MDS 倾向综合征患者进行骨髓增生异常综合征(MDS)的诊断。然而,儿科患者获得性改变的范围和后果尚未得到充分评估,尤其是在潜在综合征的背景下。我们在遗传性或获得性血细胞减少症的儿科和青年患者中纳入了一个针对 54 个基因的靶向下一代测序面板,以检测体细胞突变。本研究共纳入 65 例患者,其中 17 例(26%)存在体细胞突变。我们在 20%的遗传性 MDS 倾向综合征患者中检测到体细胞突变,包括严重先天性中性粒细胞减少症和范可尼贫血患者,以及 SAMD9L 的种系突变。38%的获得性血细胞减少症和疑似 MDS 的儿童存在体细胞改变,最常见于信号转导和转录相关基因。分子异常克隆通常先于细胞遗传学改变。因此,常规进行体细胞面板检测可以在白血病发生之前,建立 MDS 的诊断,并确定造血干细胞移植的最佳时机。此外,在具有遗传性 MDS 倾向综合征的患者中进行体细胞面板检测可能会揭示其独特的获得性突变谱。

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