Clinical and biological significance of isolated Y chromosome loss in myelodysplastic syndromes and chronic myelomonocytic leukemia. A report from the Spanish MDS Group

医学 三体8 白血病 细胞遗传学 细胞减少 髓系白血病 骨髓
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
出处
期刊:Leukemia Research [Elsevier BV]
卷期号:63: 85-89 被引量:6
标识
DOI:10.1016/j.leukres.2017.10.011
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.
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