de Swart Louise, Smith Alex, Johnston Thomas W, Haase Detlef, Droste Jackie, Fenaux Pierre, Symeonidis Argiris, Sanz Guillermo, Hellström-Lindberg Eva, Cermák Jaroslav, Germing Ulrich, Stauder Reinhard, Georgescu Otilia, MacKenzie Marius, Malcovati Luca, Holm Mette S, Almeida Antonio M, Mądry Krzysztof, Slama Borhane, Guerci-Bresler Agnes, Sanhes Laurence, Beyne-Rauzy Odile, Luño Elisa, Bowen David, de Witte Theo
Department of Haematology, Radboud University Medical Centre, Nijmegen, The Netherlands.
Epidemiology and Cancer Statistics Group, University of York, York, UK.
Br J Haematol. 2015 Aug;170(3):372-83. doi: 10.1111/bjh.13450. Epub 2015 Apr 24.
Baseline characteristics, disease-management and outcome of 1000 lower-risk myelodysplastic syndrome (MDS) patients within the European LeukaemiaNet MDS (EUMDS) Registry are described in conjunction with the validation of the revised International Prognostic Scoring System (IPSS-R). The EUMDS registry confirmed established prognostic factors, such as age, gender and World Health Organization 2001 classification. Low quality of life (EQ-5D visual analogue scale score) was significantly associated with reduced survival. A high co-morbidity index predicted poor outcome in univariate analyses. The IPSS-R identified a large group of 247 patients with Low (43%) and Very low (23%) risk score within the IPSS intermediate-1 patients. The IPSS-R also identified 32 High or Very high risk patients within the IPSS intermediate-1 patients. IPSS-R was superior to the IPSS for predicting both disease progression and survival. Seventy percent of patients received MDS-specific treatment or supportive care, including red blood cell transfusions (51%), haematopoietic growth factors (58%) and iron chelation therapy (8%), within 2 years of diagnosis; while 30% of the patients only required active monitoring. The IPSS-R proved its utility as a more refined risk stratification tool for the identification of patients with a very good or poor prognosis and in this lower-risk MDS population.
结合修订后的国际预后评分系统(IPSS-R)的验证,描述了欧洲白血病网骨髓增生异常综合征(MDS)登记处1000例低风险骨髓增生异常综合征(MDS)患者的基线特征、疾病管理和预后情况。欧洲MDS登记处证实了既定的预后因素,如年龄、性别和世界卫生组织2001年分类。生活质量低下(EQ-5D视觉模拟量表评分)与生存率降低显著相关。在单因素分析中,高合并症指数预示着预后不良。IPSS-R在IPSS中等-1组患者中识别出一大组247例低风险(43%)和极低风险(23%)评分的患者。IPSS-R还在IPSS中等-1组患者中识别出32例高风险或极高风险患者。在预测疾病进展和生存方面,IPSS-R优于IPSS。70%的患者在诊断后2年内接受了MDS特异性治疗或支持性护理,包括红细胞输注(51%)、造血生长因子(58%)和铁螯合疗法(8%);而30%的患者仅需要进行积极监测。在这一低风险MDS人群中,IPSS-R证明了其作为一种更精细的风险分层工具在识别预后非常好或非常差的患者方面的效用。