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dc.contributor.authorClark, A
dc.contributor.authorThomas, S
dc.contributor.authorHamblin, A
dc.contributor.authorTalley, P
dc.contributor.authorKulasekararaj, A
dc.contributor.authorGrinfeld, J
dc.contributor.authorSpeight, B
dc.contributor.authorSnape, K
dc.contributor.authorMcVeigh, TP
dc.contributor.authorSnowden, JA
dc.coverage.spatialEngland
dc.date.accessioned2023-05-05T13:45:29Z
dc.date.available2023-05-05T13:45:29Z
dc.date.issued2023-04-01
dc.identifier.citationBritish Journal of Haematology, 2023, 201 (1), pp. 35 - 44en_US
dc.identifier.issn0007-1048
dc.identifier.urihttps://repository.icr.ac.uk/handle/internal/5780
dc.identifier.eissn1365-2141
dc.identifier.eissn1365-2141
dc.identifier.doi10.1111/bjh.18682
dc.description.abstractGermline 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).
dc.formatPrint-Electronic
dc.format.extent35 - 44
dc.languageeng
dc.language.isoengen_US
dc.publisherWILEYen_US
dc.relation.ispartofBritish Journal of Haematology
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en_US
dc.subjectBMT
dc.subjectLeukaemia
dc.subjectgermline cancer predisposition
dc.subjecttransplant donor selection
dc.subjectHumans
dc.subjectBone Marrow
dc.subjectState Medicine
dc.subjectHematologic Neoplasms
dc.subjectGenetic Predisposition to Disease
dc.subjectGerm-Line Mutation
dc.subjectHematopoietic Stem Cell Transplantation
dc.subjectGenomics
dc.subjectTranscription Factors
dc.subjectUnited Kingdom
dc.titleManagement 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).en_US
dc.typeJournal Article
dcterms.dateAccepted2023-01-20
dc.date.updated2023-05-05T13:44:31Z
rioxxterms.versionVoRen_US
rioxxterms.versionofrecord10.1111/bjh.18682en_US
rioxxterms.licenseref.startdate2023-04-01
rioxxterms.typeJournal Article/Reviewen_US
pubs.author-urlhttps://www.ncbi.nlm.nih.gov/pubmed/36786081
pubs.issue1
pubs.organisational-group/ICR
pubs.organisational-group/ICR/Primary Group
pubs.organisational-group/ICR/Primary Group/ICR Divisions
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology
pubs.organisational-group/ICR/Primary Group/Royal Marsden Clinical Units
pubs.organisational-group/ICR/Primary Group/ICR Divisions/Genetics and Epidemiology/Cancer Genetics Education & Quality Improvement
pubs.publication-statusPublished
pubs.publisher-urlhttp://dx.doi.org/10.1111/bjh.18682
pubs.volume201
icr.researchteamCancer Genetics Edu&Qualen_US
dc.contributor.icrauthorMcVeigh, Terri
icr.provenanceDeposited by Mr Arek Surman on 2023-05-05. Deposit type is initial. No. of files: 1. Files: Br J Haematol - 2023 - Clark - Management of patients with germline predisposition to haematological malignancies.pdf


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