Suppr超能文献

国际预后评分系统(IPSS)高危核型作为清髓性干细胞移植后骨髓增生异常综合征患者预后的预测指标

IPSS poor-risk karyotype as a predictor of outcome for patients with myelodysplastic syndrome following myeloablative stem cell transplantation.

作者信息

Nevill Thomas J, Shepherd John D, Sutherland Heather J, Abou Mourad Yasser R, Lavoie Julye C, Barnett Michael J, Nantel Stephen H, Toze Cynthia L, Hogge Donna E, Forrest Donna L, Song Kevin W, Power Maryse M, Nitta Janet Y, Dai Yunfeng, Smith Clayton A

机构信息

The Leukemia/BMT Program of British Columbia, Division of Hematology, Vancouver General Hospital, British Columbia Cancer Agency and the University of British Columbia, Vancouver, BC, Canada.

出版信息

Biol Blood Marrow Transplant. 2009 Feb;15(2):205-13. doi: 10.1016/j.bbmt.2008.11.015.

Abstract

The optimal therapy for myelodysplastic syndrome (MDS) is allogeneic bone marrow (BM) or blood (BSC) stem cell transplantation (SCT), although outcomes are limited by nonrelapse mortality (NRM) and relapse. A retrospective review was performed of 156 patients who underwent SCT (114 BM, 42 BSC) for MDS or secondary acute myelogenous leukemia (sAML) at our institution. Fifty-five patients remain in continuous complete remission: 35 BM recipients and 20 BSC recipients (median follow-up 139 and 89 months, respectively). Estimated 7-year event-free survival (EFS), NRM, and risk of relapse (ROR) are 33% (95% confidence intervals [CI] 25%-43%), 42% (CI 33%-51%), and 25% (CI 17%-33%) for the BM cohort and 45% (CI 32%-64%, P= .07), 32% (CI 18%-47%, P= .15), and 23% (CI 11%-37%, P= .79) for the BSC cohort. Multivariate analysis showed IPSS poor-risk cytogenetics (P< .001), time from diagnosis to SCT (P< .001), FAB subgroup (P= .001), recipients not in complete remission (CR1) at SCT (P= .005), and the development of acute graft-versus-host disease (aGVHD) (P= .04) were all predictive of an inferior EFS. The FAB subgroup (P= .002), poor-risk karyotype (P= .004), and non-CR1 status also correlated with ROR in multivariate analysis. EFS for poor-risk karyotype patients was superior after receiving BSC compared to BM (39% versus 6%, P< .001). SCT outcomes in MDS/sAML are strongly associated with the IPSS cytogenetic risk group, although the use of BSC in poor-risk karyotype patients may lead to a more favorable long-term EFS.

摘要

骨髓增生异常综合征(MDS)的最佳治疗方法是异基因骨髓(BM)或血液(BSC)干细胞移植(SCT),尽管其疗效受到非复发死亡率(NRM)和复发的限制。我们对本机构156例因MDS或继发性急性髓系白血病(sAML)接受SCT(114例为BM,42例为BSC)的患者进行了回顾性研究。55例患者仍处于持续完全缓解状态:35例BM受者和20例BSC受者(中位随访时间分别为139个月和89个月)。BM队列的估计7年无事件生存率(EFS)、NRM和复发风险(ROR)分别为33%(95%置信区间[CI]25%-43%)、42%(CI 33%-51%)和25%(CI 17%-33%),BSC队列分别为45%(CI 32%-64%,P=0.07)、32%(CI 18%-47%,P=0.15)和23%(CI 11%-37%,P=0.79)。多变量分析显示,国际预后评分系统(IPSS)的高危细胞遗传学(P<0.001)、从诊断到SCT的时间(P<0.001)、法国-美国-英国(FAB)亚组(P=0.001)、SCT时未处于完全缓解(CR1)的受者(P=0.005)以及急性移植物抗宿主病(aGVHD)的发生(P=0.04)均提示EFS较差。FAB亚组(P=0.002)、高危核型(P=0.004)和非CR1状态在多变量分析中也与ROR相关。高危核型患者接受BSC后的EFS优于接受BM后的EFS(39%对6%,P<0.001)。MDS/sAML的SCT疗效与IPSS细胞遗传学风险组密切相关,尽管高危核型患者使用BSC可能会带来更有利的长期EFS。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验