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考虑接受异基因血液和骨髓移植的血液系统恶性肿瘤种系易感性患者的管理:英国癌症遗传学小组(UKCGG)、加拿大基因-加拿大变异(CanGene-CanVar)、英国国家医疗服务体系(NHS)英格兰基因组实验室中心(GLH)血液系统恶性肿瘤工作组以及英国血液和骨髓移植与细胞治疗学会(BSBMTCT)的最佳实践共识指南

Management of patients with germline predisposition to haematological malignancies considered for allogeneic blood and marrow transplantation: Best practice consensus guidelines from the UK Cancer Genetics Group (UKCGG), CanGene-CanVar, NHS England Genomic Laboratory Hub (GLH) Haematological Malignancies Working Group and the British Society of Blood and Marrow Transplantation and cellular therapy (BSBMTCT).

作者信息

Clark Andrew, Thomas Sally, Hamblin Angela, Talley Polly, Kulasekararaj Austin, Grinfeld Jacob, Speight Beverley, Snape Katie, McVeigh Terri P, Snowden John A

机构信息

Scottish BMT and Cellular Therapy Programme, Queen Elizabeth University Hospital, Glasgow, Scotland.

Department of Haematology, Sheffield Teaching Hospitals NHS Foundation Trust, Royal Hallamshire Hospital, Sheffield, UK.

出版信息

Br J Haematol. 2023 Apr;201(1):35-44. doi: 10.1111/bjh.18682. Epub 2023 Feb 14.

Abstract

Germline predisposition to haematological cancers is increasingly being recognised. Widespread adoption of high-throughput and whole genome sequencing is identifying large numbers of causative germline mutations. Constitutional pathogenic variants in six genes (DEAD-box helicase 41 [DDX41], ETS variant transcription factor 6 [ETV6], CCAAT enhancer binding protein alpha [CEBPA], RUNX family transcription factor 1 [RUNX1], ankyrin repeat domain containing 26 [ANKRD26] and GATA binding protein 2 [GATA2]) are particularly significant in increasing the risk of haematological cancers, with variants in some of these genes also associated with non-malignant syndromic features. Allogeneic blood and marrow transplantation (BMT) is central to management in many haematological cancers. Identification of germline variants may have implications for the patient and potential family donors. Beyond selection of an appropriate haematopoietic stem cell donor there may be sensitive issues surrounding identification and counselling of hitherto asymptomatic relatives. If BMT is needed, there is frequently a clinical urgency that demands a rapid integrated multidisciplinary approach to testing and decision making involving haematologists in collaboration with Clinical and Laboratory Geneticists. Here, we present best practice consensus guidelines arrived at following a meeting convened by the UK Cancer Genetics Group (UKCGG), the Cancer Research UK (CRUK) funded CanGene-CanVar research programme (CGCV), NHS England Genomic Laboratory Hub (GLH) Haematological Oncology Malignancies Working Group and the British Society of Blood and Marrow Transplantation and Cellular Therapy (BSBMTCT).

摘要

人们越来越认识到种系因素易患血液系统癌症。高通量和全基因组测序的广泛应用正在识别大量致病种系突变。六个基因(DEAD盒解旋酶41 [DDX41]、ETS变异转录因子6 [ETV6]、CCAAT增强子结合蛋白α [CEBPA]、RUNX家族转录因子1 [RUNX1]、含锚蛋白重复结构域26 [ANKRD26] 和GATA结合蛋白2 [GATA2])中的遗传性致病变异在增加血液系统癌症风险方面尤为显著,其中一些基因的变异还与非恶性综合征特征相关。异基因造血干细胞移植(BMT)是许多血液系统癌症治疗的核心。种系变异的识别可能对患者及其潜在的家庭供体产生影响。除了选择合适的造血干细胞供体之外,围绕识别和咨询迄今无症状的亲属可能还存在敏感问题。如果需要进行BMT,通常存在临床紧迫性,这就要求采用快速的综合多学科方法进行检测和决策,血液科医生要与临床和实验室遗传学家合作。在此,我们介绍了英国癌症遗传学小组(UKCGG)、英国癌症研究(CRUK)资助的CanGene-CanVar研究项目(CGCV)、英国国家医疗服务体系(NHS)英格兰基因组实验室中心(GLH)血液肿瘤恶性肿瘤工作组以及英国血液和骨髓移植与细胞治疗协会(BSBMTCT)召开会议后达成的最佳实践共识指南。

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