作者
Meritxell Nomdedeu,Arturo Pereira,Xavier Calvo,Joan Colomer,Francesc Solé,Amparo Arias,Cándida Gómez,Elisa Luño,José Cervera,Montserrat Arnan,Helena Pomares,Fernando Ramos,Itziar Oiartzabal,Blanca Espinet,Carme Pedro,Beatriz Arrizabalaga,María Laura Blanco,Mar Tormo,Jesús María Hernández-Rivas,María Díez-Campelo,Margarita Ortega,David Valcárcel,Maria-Teresa Cedena,Rosa Collado,Javier Grau,Isabel Granada,Guillermo Sanz,Elias Campo,Jordi Esteve,Dolors Costa
摘要
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.