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).
Andrew ClarkSally ThomasAngela HamblinPolly TalleyAustin G KulasekararajJacob GrinfeldBeverley SpeightKatie SnapeTerri Patricia McVeighJohn A SnowdenPublished in: British journal of haematology (2023)
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).
Keyphrases
- transcription factor
- binding protein
- bioinformatics analysis
- genome wide identification
- papillary thyroid
- copy number
- stem cells
- dna binding
- dna repair
- clinical practice
- squamous cell
- high throughput
- healthcare
- stem cell transplantation
- cell therapy
- childhood cancer
- primary care
- bone marrow
- decision making
- genome wide
- randomized controlled trial
- lymph node metastasis
- cross sectional
- patient safety
- gene expression
- acute lymphoblastic leukemia
- dna damage
- network analysis
- autism spectrum disorder
- study protocol
- human immunodeficiency virus
- squamous cell carcinoma
- high dose
- hepatitis c virus
- human health
- case report
- climate change