同种异体移植治疗相关性骨髓增生异常综合征和急性髓系白血病。

Allogeneic transplantation for therapy-related myelodysplastic syndrome and acute myeloid leukemia.

机构信息

Mayo Clinic Rochester, Rochester, MN, USA.

出版信息

Blood. 2010 Mar 4;115(9):1850-7. doi: 10.1182/blood-2009-10-249128. Epub 2009 Dec 23.

Abstract

Therapy-related myelodysplastic syndromes (t-MDSs) and acute myeloid leukemia (t-AML) have a poor prognosis with conventional therapy. Encouraging results are reported after allogeneic transplantation. We analyzed outcomes in 868 persons with t-AML (n = 545) or t-MDS (n = 323) receiving allogeneic transplants from 1990 to 2004. A myeloablative regimen was used for conditioning in 77%. Treatment-related mortality (TRM) and relapse were 41% (95% confidence interval [CI], 38-44) and 27% (24-30) at 1 year and 48% (44-51) and 31% (28-34) at 5 years, respectively. Disease-free (DFS) and overall survival (OS) were 32% (95% CI, 29-36) and 37% (34-41) at 1 year and 21% (18-24) and 22% (19-26) at 5 years, respectively. In multivariate analysis, 4 risk factors had adverse impacts on DFS and OS: (1) age older than 35 years; (2) poor-risk cytogenetics; (3) t-AML not in remission or advanced t-MDS; and (4) donor other than an HLA-identical sibling or a partially or well-matched unrelated donor. Five-year survival for subjects with none, 1, 2, 3, or 4 of these risk factors was 50% (95% CI, 38-61), 26% (20-31), 21% (16-26), 10% (5-15), and 4% (0-16), respectively (P < .001). These data permit a more precise prediction of outcome and identify subjects most likely to benefit from allogeneic transplantation.

摘要

治疗相关的骨髓增生异常综合征(t-MDSs)和急性髓系白血病(t-AML)采用常规疗法预后较差。异体移植后报告了令人鼓舞的结果。我们分析了 1990 年至 2004 年期间接受异体移植的 868 名 t-AML(n = 545)或 t-MDS(n = 323)患者的结局。77%的患者采用清髓性预处理方案。1 年时,治疗相关死亡率(TRM)和复发率分别为 41%(95%可信区间[CI],38-44)和 27%(24-30),5 年时分别为 48%(44-51)和 31%(28-34)。无病生存(DFS)和总生存(OS)分别为 1 年时 32%(95%CI,29-36)和 37%(34-41),5 年时 21%(18-24)和 22%(19-26)。多变量分析显示,4 个危险因素对 DFS 和 OS 有不利影响:(1)年龄大于 35 岁;(2)不良核型;(3)t-AML 未缓解或晚期 t-MDS;(4)供者非 HLA 全相合同胞或部分或全相合无关供者。无、1、2、3、4 个危险因素的患者 5 年生存率分别为 50%(95%CI,38-61)、26%(20-31)、21%(16-26)、10%(5-15)和 4%(0-16)(P<0.001)。这些数据可以更准确地预测结局,并确定最有可能从异体移植中获益的患者。

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