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)

Author:

Clark Andrew1ORCID,Thomas Sally2,Hamblin Angela3,Talley Polly4,Kulasekararaj Austin5ORCID,Grinfeld Jacob6,Speight Beverley7ORCID,Snape Katie8,McVeigh Terri P.9ORCID,Snowden John A.10ORCID

Affiliation:

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

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

3. Department of Haematology Oxford University Hospitals NHS Foundation Trust, Churchill Hospital Oxford UK

4. Haematological Malignancy Diagnostic Service (HMDS) St James's University Hospital Leeds UK

5. Department of Haematological Medicine King's College Hospital Denmark Hill, London and King's College London London UK

6. Department of Paediatric Haematology and Oncology Leeds Childrens Hospital Leeds UK

7. East Anglian Medical Genetics Service Cambridge UK

8. South West Thames Regional Genetics Service St George's University Hospitals NHS Foundation Trust London UK

9. Cancer Genetics Unit Royal Marsden NHS Foundation Trust London UK

10. Department of Haematology Sheffield BMT and Cellular Therapy Programme Sheffield Teaching Hospitals NHS Foundation Trust Sheffield UK

Abstract

SummaryGermline 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).

Publisher

Wiley

Subject

Hematology

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3