Nomdedeu Meritxell, Pereira Arturo, Calvo Xavier, Colomer Joan, Sole Francesc, Arias Amparo, Gomez Candida, Luño Elisa, Cervera Jose, Arnan Montserrat, Pomares Helena, Ramos Fernando, Oiartzabal Itziar, Espinet Blanca, Pedro Carme, Arrizabalaga Beatriz, Blanco María Laura, Tormo Mar, Hernandez-Rivas Jesus Maria, Díez-Campelo María, Ortega Margarita, Valcárcel David, Cedena Maria-Teresa, Collado Rosa, Grau Javier, Granada Isabel, Sanz Guillermo, Campo Elias, Esteve Jordi, Costa Dolors
Hospital Plató, Barcelona, Spain; Fundació Clínic per la Recerca Biomèdica, Barcelona, Spain.
Hospital Clinic-IDIBAPS, Barcelona, Spain.
Leuk Res. 2017 Dec;63:85-89. doi: 10.1016/j.leukres.2017.10.011. Epub 2017 Oct 28.
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.
骨髓增生异常综合征(MDS)中Y染色体缺失(-Y)与较好的预后相关,但它也被充分描述为一种与年龄相关的现象。在本研究中,我们旨在分析在国际预后评分系统修订版(IPSS-R)细胞遗传学分类背景下-Y的预后影响,评估具有孤立-Y的中期细胞百分比的临床意义,并测试发现-Y是否可能导致对具有临界形态学特征的患者过度诊断为MDS。我们评估了来自西班牙MDS登记处的3581例诊断为MDS或慢性粒单核细胞白血病(CMML)的男性患者。177例患者(4.9%)检测到-Y。与2246例核型正常的男性患者相比,-Y组白血病转化风险降低,但这并未转化为生存优势。总体生存和白血病转化风险不受具有-Y的中期细胞百分比的影响。-Y组中具有轻微发育异常形态特征的患者并未富集,这表明-Y组较好的预后不能用误诊为MDS的病例富集来解释。总之,我们的结果支持目前将具有-Y的患者分类为IPSS-R中MDS的极佳风险类别的建议,并排除选择偏倚作为这种较好预后的可能解释。对具有孤立-Y的MDS的分子基础进行分析将很有意义,因为它可能提供防止进展为急性白血病的生物学基础。