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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).
Clark, Andrew; Thomas, Sally; Hamblin, Angela; Talley, Polly; Kulasekararaj, Austin; Grinfeld, Jacob; Speight, Beverley; Snape, Katie; McVeigh, Terri P; Snowden, John A.
Afiliação
  • Clark A; Scottish BMT and Cellular Therapy Programme, Queen Elizabeth University Hospital, Glasgow, Scotland.
  • Thomas S; Department of Haematology, Sheffield Teaching Hospitals NHS Foundation Trust, Royal Hallamshire Hospital, Sheffield, UK.
  • Hamblin A; Department of Haematology, Oxford University Hospitals NHS Foundation Trust, Churchill Hospital, Oxford, UK.
  • Talley P; Haematological Malignancy Diagnostic Service (HMDS), St James's University Hospital, Leeds, UK.
  • Kulasekararaj A; Department of Haematological Medicine, King's College Hospital, Denmark Hill, London and King's College London, London, UK.
  • Grinfeld J; Department of Paediatric Haematology and Oncology, Leeds Childrens Hospital, Leeds, UK.
  • Speight B; East Anglian Medical Genetics Service, Cambridge, UK.
  • Snape K; South West Thames Regional Genetics Service, St George's University Hospitals NHS Foundation Trust, London, UK.
  • McVeigh TP; Cancer Genetics Unit, Royal Marsden NHS Foundation Trust, London, UK.
  • Snowden JA; Department of Haematology, Sheffield BMT and Cellular Therapy Programme, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK.
Br J Haematol ; 201(1): 35-44, 2023 04.
Article em En | MEDLINE | ID: mdl-36786081
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).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Neoplasias Hematológicas Tipo de estudo: Guideline / Prognostic_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2023 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Transplante de Células-Tronco Hematopoéticas / Neoplasias Hematológicas Tipo de estudo: Guideline / Prognostic_studies Limite: Humans País como assunto: Europa Idioma: En Ano de publicação: 2023 Tipo de documento: Article