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在诊断时具有不良细胞遗传学特征的急性髓细胞白血病患者,在缓解期接受 HLA 高匹配的无关供者或同胞供者移植后的生存情况相当。

Comparable survival after HLA-well-matched unrelated or matched sibling donor transplantation for acute myeloid leukemia in first remission with unfavorable cytogenetics at diagnosis.

机构信息

Princess Margaret Hospital, University of Toronto, Toronto, Ontario.

出版信息

Blood. 2010 Sep 16;116(11):1839-48. doi: 10.1182/blood-2010-04-278317. Epub 2010 Jun 10.

DOI:10.1182/blood-2010-04-278317
PMID:20538804
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3173984/
Abstract

We compared the outcomes of unrelated donor (URD, n = 358) with human leukocyte antigen (HLA)-matched sibling donor (MSD, n = 226) transplantations in patients with acute myeloid leukemia (AML) in first complete remission (CR1) having unfavorable cytogenetics at diagnosis. Unfavorable cytogenetic abnormalities were: complex (≥ 3 abnormalities), 32%; and noncomplex involving chromosome 7, 25%; chromosome 5, 9%; 11q or MLL rearrangements, 18%; t(6;9), 5%; and other noncomplex, 10%. URDs were HLA-well-matched (n = 254; 71%) or partially-matched (n = 104; 29%). Three-year leukemia-free survival (LFS) for MSD was 42% (95% confidence interval [CI], 35%-48%) compared with 34% (95% CI, 28%-41%) for HLA-well-matched URD and 29% (95% CI, 20%-39%) for partially-matched URD (P = .08). In multivariate analysis, HLA-well-matched URD and MSD yielded similar LFS (relative risk [RR] = 1.1, 95% CI, 0.86-1.40, P = .44) and overall survival (OS; RR = 1.06, 95% CI, 0.83-1.37, P = .63). LFS and OS were significantly inferior for HLA-partially-matched URD recipients, those with prior myelodysplastic syndrome, and those older than 50 years. All cytogenetic cohorts had similar outcomes. Patients with chronic graft-versus-host disease had a significantly lower risk of relapse (RR = 0.68, 95% CI, 0.47-0.99, P = .05). Hematopoietic cell transplantation (HCT) using HLA-well-matched URD and MSD resulted in similar LFS and OS in AML patients in CR1 with unfavorable cytogenetics. Outcomes of HCT from HLA-partially- matched URD were inferior.

摘要

我们比较了在初诊时伴有不良细胞遗传学的急性髓系白血病(AML)患者中,无关供体(URD,n = 358)与人类白细胞抗原(HLA)匹配的同胞供体(MSD,n = 226)移植的结果。不良细胞遗传学异常包括:复杂(≥ 3 种异常),32%;非复杂涉及染色体 7,25%;染色体 5,9%;11q 或 MLL 重排,18%;t(6;9),5%;以及其他非复杂,10%。URD 为 HLA 高度匹配(n = 254;71%)或部分匹配(n = 104;29%)。MSD 的 3 年无白血病生存率(LFS)为 42%(95%置信区间[CI],35%-48%),而 HLA 高度匹配 URD 为 34%(95% CI,28%-41%),部分匹配 URD 为 29%(95% CI,20%-39%)(P =.08)。多变量分析显示,HLA 高度匹配 URD 和 MSD 的 LFS 相似(相对风险[RR] = 1.1,95% CI,0.86-1.40,P =.44)和总生存(OS;RR = 1.06,95% CI,0.83-1.37,P =.63)。HLA 部分匹配 URD 受体、有先前骨髓增生异常综合征和年龄大于 50 岁的患者的 LFS 和 OS 显著降低。所有细胞遗传学队列的结果相似。患有慢性移植物抗宿主病的患者复发风险显著降低(RR = 0.68,95% CI,0.47-0.99,P =.05)。使用 HLA 高度匹配 URD 和 MSD 的造血细胞移植(HCT)在伴有不良细胞遗传学的 CR1 期 AML 患者中产生了相似的 LFS 和 OS。HLA 部分匹配 URD 的 HCT 结果较差。

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