Enrico Alicia, Bestach Yesica, Flores Maria Gabriela, Arbelbide Jorge, Serale Camila, Novoa Viviana, Crisp Renée, Rivas María Marta, Larripa Irene, Belli Carolina
Area de Hematología, Hospital Italiano de La Plata, La Plata, Argentina.
Laboratorio de Genética Hematológica, Instituto de Medicina Experimental, Consejo Nacional de Investigaciones Científicas y Técnicas/Academia Nacional de Medicina, Buenos Aires City, Argentina.
Clin Lymphoma Myeloma Leuk. 2017 Nov;17(11):743-752.e5. doi: 10.1016/j.clml.2017.06.024. Epub 2017 Jun 23.
A large group of patients with myelodysplastic syndromes (MDS) will die of causes intrinsic to bone marrow failure. One third of patients will develop acute myeloid leukemia (AML), which is associated with an extremely poor outcome and a short survival. Our objectives were to analyze the prognostic variables and scoring systems in the attempt to determine the influence of progression on the overall survival of MDS patients.
We performed a retrospective analysis of 831 MDS patients, including those from the Argentine Registry.
Of the 831 MDS patients, 158 (19.0%) experienced transformation, with a median overall survival of 17.9 months from diagnosis and 3.5 months after progression. The survival of patients with adverse karyotypes or greater risk, according to the International Prognostic Scoring System-revised (IPSS-R) or World Health Organization-based Prognostic Scoring System (WPSS) was not affected when stratified by patients with and without evolution to AML (P > .05). In contrast, the survival of lower risk patients was significantly reduced for those patients with progression to AML (P < .001) and those younger (P = .024) than those who died of non-AML-related causes. The intermediate-risk patients were heterogeneously distributed; however, an upgrade from a lower IPSS-R to a higher WPSS-hemoglobin risk category was associated with a worse outcome, not affected by progression (P = .420), with a median event-free survival of 16 months.
The use of the IPSS-R and WPSS systems simultaneously might help in identifying those patients who require more aggressive treatment. Nevertheless, more efforts are needed to improve the identification of those lower risk patients whose survival is significantly reduced by progression to AML.
一大群骨髓增生异常综合征(MDS)患者将死于骨髓衰竭的内在原因。三分之一的患者会发展为急性髓系白血病(AML),这与极差的预后和较短的生存期相关。我们的目的是分析预后变量和评分系统,以试图确定疾病进展对MDS患者总生存期的影响。
我们对831例MDS患者进行了回顾性分析,包括来自阿根廷登记处的患者。
在831例MDS患者中,158例(19.0%)发生了转化,从诊断开始的中位总生存期为17.9个月,进展后的中位总生存期为3.5个月。根据修订的国际预后评分系统(IPSS-R)或基于世界卫生组织的预后评分系统(WPSS),不良核型或更高风险患者的生存期,在按是否演变为AML进行分层时不受影响(P>.05)。相比之下,进展为AML的低风险患者的生存期显著缩短(P<.001),且比死于非AML相关原因的患者年轻(P=.024)。中风险患者分布不均;然而,从较低的IPSS-R升级到较高的WPSS-血红蛋白风险类别与更差的预后相关,不受疾病进展影响(P=.420),无事件生存期的中位数为16个月。
同时使用IPSS-R和WPSS系统可能有助于识别那些需要更积极治疗的患者。然而,仍需要更多努力来改善对那些生存期因进展为AML而显著缩短的低风险患者的识别。