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低危骨髓增生异常综合征患者的预后评分

A prognostic score for patients with lower risk myelodysplastic syndrome.

作者信息

Garcia-Manero G, Shan J, Faderl S, Cortes J, Ravandi F, Borthakur G, Wierda W G, Pierce S, Estey E, Liu J, Huang X, Kantarjian H

机构信息

Department of Leukemia, University of Texas MD Anderson Cancer Center, Houston, TX 77030, USA.

出版信息

Leukemia. 2008 Mar;22(3):538-43. doi: 10.1038/sj.leu.2405070. Epub 2007 Dec 13.

Abstract

Current prognostic models for myelodysplastic syndromes (MDS) do not allow the identification of patients with lower risk disease and poor prognosis that may benefit from early therapeutic intervention. We evaluated the characteristics of 856 patients with low or intermediate-1 disease by the International Prognostic Scoring System. Mean follow-up was 19.6 months (range 1-262). Of these patients, 87 (10%) transformed to acute myelogenous leukemia, and 429 (50%) had died. By multivariate analysis, characteristics associated with worse survival (P<0.01) were low platelets, anemia, older age, higher percent of marrow blasts and poor-risk cytogenetics. Although not included in the model, higher ferritin (P=0.007) and beta2-microglobulin (P<0.001) levels were associated with worse prognosis. This allowed the development of a scoring system in which patients could be grouped in three categories: category 1 (n=182, 21%) with a median survival of 80.3 months (95% CI 68-NA); category 2 (n=408, 48%) with a median survival of 26.6 months (95% CI 22-32) and category 3 (n=265, 31%) with a median survival of 14.2 months (95% CI 13-18). In summary, this analysis indicates that it is possible to identify patients with lower risk MDS and poor prognosis who may benefit from early intervention.

摘要

目前用于骨髓增生异常综合征(MDS)的预后模型无法识别出那些患有低风险疾病但预后较差、可能从早期治疗干预中获益的患者。我们通过国际预后评分系统评估了856例低危或中危1级疾病患者的特征。平均随访时间为19.6个月(范围1 - 262个月)。在这些患者中,87例(10%)转化为急性髓系白血病,429例(50%)死亡。通过多变量分析,与较差生存(P<0.01)相关的特征为血小板计数低、贫血、年龄较大、骨髓原始细胞百分比高以及高危细胞遗传学。虽然未纳入模型,但较高的铁蛋白水平(P = 0.007)和β2 - 微球蛋白水平(P<0.001)与较差的预后相关。这使得能够开发一种评分系统,根据该系统患者可分为三类:第1类(n = 182,21%),中位生存期为80.3个月(95% CI 68 - 无上限);第2类(n = 408,48%),中位生存期为26.6个月(95% CI 22 - 32);第3类(n = 265,31%),中位生存期为14.2个月(95% CI 13 - 18)。总之,该分析表明有可能识别出那些患有低风险MDS但预后较差、可能从早期干预中获益的患者。

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