| Literature DB >> 31484648 |
Marie Sébert1,2,3, Marie Passet2,3,4, Anna Raimbault2,3,4, Ramy Rahmé1,3, Emmanuel Raffoux5, Flore Sicre de Fontbrune6, Marco Cerrano5, Samuel Quentin2,4, Nadia Vasquez4, Mélanie Da Costa4, Nicolas Boissel3,5, Hervé Dombret3,5, Régis Peffault de Latour3,6, Gérard Socié3,6, Raphaël Itzykson2,3,5, Pierre Fenaux1,2,3, Jean Soulier2,3,4, Lionel Adès1,2,3, Emmanuelle Clappier2,3,4.
Abstract
Germline DDX41 mutations are involved in familial myelodysplastic syndromes (MDSs) and acute myeloid leukemias (AMLs). We analyzed the prevalence and characteristics of DDX41-related myeloid malignancies in an unselected cohort of 1385 patients with MDS or AML. Using targeted next-generation sequencing, we identified 28 different germline DDX41 variants in 43 unrelated patients, which we classified as causal (n = 21) or unknown significance (n = 7) variants. We focused on the 33 patients having causal variants, representing 2.4% of our cohort. The median age was 69 years; most patients were men (79%). Only 9 patients (27%) had a family history of hematological malignancy, and 15 (46%) had a personal history of cytopenia years before MDS/AML diagnosis. Most patients had a normal karyotype (85%), and the most frequent somatic alteration was a second DDX41 mutation (79%). High-risk DDX41 MDS/AML patients treated with intensive chemotherapy (n = 9) or azacitidine (n = 11) had an overall response rate of 100% or 73%, respectively, with a median overall survival of 5.2 years. Our study highlights that germline DDX41 mutations are relatively common in adult MDS/AML, often without known family history, arguing for systematic screening. Salient features of DDX41-related myeloid malignancies include male preponderance, frequent preexisting cytopenia, additional somatic DDX41 mutation, and relatively good outcome.Entities:
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Year: 2019 PMID: 31484648 DOI: 10.1182/blood.2019000909
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113