| Literature DB >> 29121539 |
Meritxell Nomdedeu1, Arturo Pereira2, Xavier Calvo3, Joan Colomer2, Francesc Sole4, Amparo Arias2, Candida Gomez2, Elisa Luño5, Jose Cervera6, Montserrat Arnan7, Helena Pomares7, Fernando Ramos8, Itziar Oiartzabal9, Blanca Espinet3, Carme Pedro3, Beatriz Arrizabalaga10, María Laura Blanco11, Mar Tormo12, Jesus Maria Hernandez-Rivas13, María Díez-Campelo13, Margarita Ortega14, David Valcárcel14, Maria-Teresa Cedena15, Rosa Collado16, Javier Grau17, Isabel Granada17, Guillermo Sanz6, Elias Campo2, Jordi Esteve2, Dolors Costa2.
Abstract
Isolate loss of chromosome Y (-Y) in myelodysplastic syndromes (MDS) is associated to a better outcome but it is also well described as an age-related phenomenon. In this study we aimed to analyze the prognostic impact of -Y in the context of the IPSS-R cytogenetic classification, evaluate the clinical significance of the percentage of metaphases with isolated -Y, and test whether finding -Y may predispose to over-diagnose MDS in patients with borderline morphological features. We evaluated 3581 male patients from the Spanish MDS Registry with a diagnosis of MDS or chronic myelomonocytic leukemia (CMML). -Y was identified in 177 patients (4.9%). Compared with the 2246 male patients with normal karyotype, -Y group showed a reduced risk of leukemic transformation that did not translate into a survival advantage. The overall survival and the risk of leukemic transformation were not influenced by the percentage of metaphases with -Y. The -Y group was not enriched in patients with minor morphologic traits of dysplasia, suggesting that the better outcome in the -Y group cannot be explained by enrichment in cases misdiagnosed as MDS. In conclusion, our results support the current recommendation of classifying patients with -Y within the very good risk category of the IPSS-R for MDS and rule out a selection bias as a possible explanation of this better outcome. An analysis of the molecular basis of MDS with isolated -Y would be of interest as it may provide a biological basis of protection against progression to acute leukemia.Entities:
Keywords: IPSS-R; Karyotype; Loss of chromosome Y; MDS; Prognosis
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Year: 2017 PMID: 29121539 DOI: 10.1016/j.leukres.2017.10.011
Source DB: PubMed Journal: Leuk Res ISSN: 0145-2126 Impact factor: 3.156