| Literature DB >> 31527074 |
Elise Chapiro1,2,3, Elodie Pramil1,2, M'boyba Diop4, Damien Roos-Weil1,2,5, Clémentine Dillard1,2, Clémentine Gabillaud3, Karim Maloum3, Catherine Settegrana3, Lucile Baseggio6, Jean-François Lesesve7, Mélanie Yon1,2, Ludovic Jondreville1,2, Claude Lesty2, Frédéric Davi1,2,3, Magali Le Garff-Tavernier1,3, Nathalie Droin4, Philippe Dessen4, Caroline Algrin8, Véronique Leblond2,5, Jean Gabarre5, Simon Bouzy3, Virginie Eclache9, Baptiste Gaillard10, Evelyne Callet-Bauchu6, Marc Muller11, Christine Lefebvre12, Nathalie Nadal13, Antoine Ittel14, Stéphanie Struski15, Marie-Agnès Collonge-Rame16, Benoit Quilichini17, Sandra Fert-Ferrer18, Nathalie Auger19, Isabelle Radford-Weiss20, Lena Wagner21, Sebastian Scheinost21, Thorsten Zenz22, Santos A Susin1,2, Olivier A Bernard23,24, Florence Nguyen-Khac1,2,3.
Abstract
B-cell prolymphocytic leukemia (B-PLL) is a rare hematological disorder whose underlying oncogenic mechanisms are poorly understood. Our cytogenetic and molecular assessments of 34 patients with B-PLL revealed several disease-specific features and potential therapeutic targets. The karyotype was complex (≥3 abnormalities) in 73% of the patients and highly complex (≥5 abnormalities) in 45%. The most frequent chromosomal aberrations were translocations involving MYC [t(MYC)] (62%), deletion (del)17p (38%), trisomy (tri)18 (30%), del13q (29%), tri3 (24%), tri12 (24%), and del8p (23%). Twenty-six (76%) of the 34 patients exhibited an MYC aberration, resulting from mutually exclusive translocations or gains. Whole-exome sequencing revealed frequent mutations in TP53, MYD88, BCOR, MYC, SF3B1, SETD2, CHD2, CXCR4, and BCLAF1. The majority of B-PLL used the IGHV3 or IGHV4 subgroups (89%) and displayed significantly mutated IGHV genes (79%). We identified 3 distinct cytogenetic risk groups: low risk (no MYC aberration), intermediate risk (MYC aberration but no del17p), and high risk (MYC aberration and del17p) (P = .0006). In vitro drug response profiling revealed that the combination of a B-cell receptor or BCL2 inhibitor with OTX015 (a bromodomain and extra-terminal motif inhibitor targeting MYC) was associated with significantly lower viability of B-PLL cells harboring a t(MYC). We concluded that cytogenetic analysis is a useful diagnostic and prognostic tool in B-PLL. Targeting MYC may be a useful treatment option in this disease.Entities:
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Year: 2019 PMID: 31527074 DOI: 10.1182/blood.2019001187
Source DB: PubMed Journal: Blood ISSN: 0006-4971 Impact factor: 22.113