首页> 外文期刊>Journal of Clinical Oncology >HLA-identical sibling compared with 8/8 matched and mismatched unrelated donor bone marrow transplant for chronic phase chronic myeloid leukemia.
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HLA-identical sibling compared with 8/8 matched and mismatched unrelated donor bone marrow transplant for chronic phase chronic myeloid leukemia.

机译:HLA相同的同胞与8/8匹配和不匹配的无关供体骨髓移植相比可治疗慢性阶段性慢性粒细胞白血病。

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PURPOSE: Transplantation of hematopoietic stem cells from an unrelated donor (URD) is an option for many patients who do not have an HLA-identical sibling donor (MSD). Current criteria for the selection of URDs include consideration for HLA alleles determined by high resolution typing methods, with preference for allele-matched donors. However, the utility and outcome associated with transplants from URDs compared with those from MSDs remains undefined. PATIENTS AND METHODS: We examined clinical outcome after patients received bone marrow transplants (BMTs) from MSDs; HLA-A, -B, -C, and DRB1 allele-matched URDs (8/8); and HLA-mismatched URDs in a homogeneous population of patients with chronic myeloid leukemia (CML) in first chronic phase (CP1) where a strong allogeneic effect and hence a lower risk of relapse is anticipated. Transplantation outcomes were compared between 1,052 URD and 3,514 MSD BMT recipients with CML in CP1. RESULTS: Five-year overall survival and leukemia-free survival (LFS) after receipt of BMTs from 8/8 matched URDs were worse than those after receipt of BMTs from MSDs (5-year survival, 55% v 63%; RR, 1.35; 95% CI, 1.17 to 1.56; P < .001; LFS, 50% v 55%; RR, 1.21; 95% CI, 1.06 to 1.40; P = .006). Survival was progressively worse with greater degrees of mismatch. Similar and low risk of relapse were observed after receipt of transplant from either MSD or URD. CONCLUSION: In this homogeneous cohort of good risk patients with CML in CP1, 5-year overall survival and LFS after receipt of transplant from 8/8 allele-matched donors were modestly though significantly worse than those after receipt of transplant from MSDs. Additive adverse effects of multilocus mismatching are not well tolerated and should be avoided if possible.
机译:目的:对于没有HLA同胞供者(MSD)的许多患者,从无关供者(URD)移植造血干细胞是一种选择。当前选择URD的标准包括考虑通过高分辨率分型方法确定的HLA等位基因,尤其是等位基因匹配的供体。但是,与来自MSD的URD移植相比,其实用性和结果尚不确定。患者和方法:我们检查了接受MSD骨髓移植(BMT)的患者的临床结局。 HLA-A,-B,-C和DRB1等位基因匹配的URD(8/8);和HLA不匹配的URDs在第一个慢性期(CP1)的同质慢性粒细胞白血病(CML)患者中,具有很强的同种异体作用,因此复发风险较低。比较了CP1中CML的1,052位URD和3,514位MSD BMT接受者的移植结果。结果:接受8/8匹配URD的BMT后的五年总体生存期和无白血病生存期(LFS)比接受MSD的BMT的五年总体生存期和无白血病生存期差(5年生存率,55%对63%; RR,1.35) ; 95%CI,1.17至1.56; P <.001; LFS,50%v 55%; RR,1.21; 95%CI,1.06-1.40; P = .006)。存活率随着不匹配程度的增加而逐渐恶化。从MSD或URD接受移植后,观察到复发的风险相似且低。结论:在CP1 CML的高风险患者的同质队列中,从8/8等位基因匹配的供体接受移植后的5年总生存率和LFS较适度,尽管显着低于从MSD接受移植后。多位点错配的附加不利影响不能很好地容忍,应尽可能避免。

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