Different prognostic impact of recurrent gene mutations in chronic lymphocytic leukemia depending on IGHV gene somatic hypermutation status: a study by ERIC in HARMONY.
Larry MansouriBirna ThorvaldsdottirLesley-Ann SuttonGeorgios KarakatsoulisManja MeggendorferHelen ParkerFerran NadeuChristian BrieghelStamatia LaidouRiccardo MoiaDavide RossiMark CatherwoodJana KotaskovaJulio DelgadoAna Eugenia Rodríguez VicenteRocío BenitoGian Matteo RigolinSilvia BonfiglioLydia ScarfoMattias MattssonZadie DavisAjay GogiaLata RaniPanagiotis BaliakasHassan Foroughi-AslCecilia JylhäAron SkaftasonInmaculada RapadoFatima MirasJoaquín Martinez-LopezJavier de laSernaJesús María Hernández RivasPatrick ThorntonMaría José LarráyozMaría José CalasanzViktória FésüsZoltán MátraiCsaba BödörKarin E SmedbyBlanca EspinetAnna PuiggrosRitu GuptaLars BullingerFrancesc BoschBárbara Tazón-VegaFanny Baran-MarszakDavid OscierFlorence Nguyen-KhacThorsten ZenzMaria Jose TerolAntonio CuneoMaría Hernández-SánchezSarka PospisilovaKenneth Ian MillsGianluca GaidanoCarsten Utoft NiemannElias CampoJonathan C StreffordPaolo GhiaKostas StamatopoulosRichard RosenquistPublished in: Leukemia (2022)
Recent evidence suggests that the prognostic impact of gene mutations in patients with chronic lymphocytic leukemia (CLL) may differ depending on the immunoglobulin heavy variable (IGHV) gene somatic hypermutation (SHM) status. In this study, we assessed the impact of nine recurrently mutated genes (BIRC3, EGR2, MYD88, NFKBIE, NOTCH1, POT1, SF3B1, TP53, and XPO1) in pre-treatment samples from 4580 patients with CLL, using time-to-first-treatment (TTFT) as the primary end-point in relation to IGHV gene SHM status. Mutations were detected in 1588 (34.7%) patients at frequencies ranging from 2.3-9.8% with mutations in NOTCH1 being the most frequent. In both univariate and multivariate analyses, mutations in all genes except MYD88 were associated with a significantly shorter TTFT. In multivariate analysis of Binet stage A patients, performed separately for IGHV-mutated (M-CLL) and unmutated CLL (U-CLL), a different spectrum of gene alterations independently predicted short TTFT within the two subgroups. While SF3B1 and XPO1 mutations were independent prognostic variables in both U-CLL and M-CLL, TP53, BIRC3 and EGR2 aberrations were significant predictors only in U-CLL, and NOTCH1 and NFKBIE only in M-CLL. Our findings underscore the need for a compartmentalized approach to identify high-risk patients, particularly among M-CLL patients, with potential implications for stratified management.
Keyphrases
- chronic lymphocytic leukemia
- copy number
- genome wide
- end stage renal disease
- genome wide identification
- newly diagnosed
- ejection fraction
- chronic kidney disease
- cell proliferation
- prognostic factors
- dna methylation
- genome wide analysis
- gene expression
- patient reported outcomes
- transcription factor
- inflammatory response
- replacement therapy
- bioinformatics analysis