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HistoCheck 检测 HLA Ⅰ类错配分数不能预测无关造血干细胞移植的临床结局。

Scoring HLA class I mismatches by HistoCheck does not predict clinical outcome in unrelated hematopoietic stem cell transplantation.

机构信息

Center for International Blood and Marrow Transplant Research, Minneapolis, Minnesota 55413, USA.

出版信息

Biol Blood Marrow Transplant. 2012 May;18(5):739-46. doi: 10.1016/j.bbmt.2011.09.008. Epub 2011 Sep 29.

Abstract

Currently, there is no well-accepted rating system for reliably predicting which HLA-mismatched (MM) unrelated donor should be selected for a patient without an HLA allele-matched donor. We evaluated the ability of an MM ranking system, HistoCheck, to predict the risk associated with HLA class I disparity in a population of 744 single allele or antigen HLA-A, -B, or -C MM myeloablative unrelated donor hematopoietic stem cell transplantation recipients with acute myelogenous leukemia, acute lymphoblastic leukemia, chronic myelogenous leukemia, or myelodysplastic syndrome, facilitated through the National Marrow Donor Program between 1988 and 2003. Multivariate models were used to adjust for other significant clinical risk factors. HLA MMs were scored using the HistoCheck Web-based tool, and the patients were divided into 4 quartiles: dissimilarity score (DSS) 1.04-2.84 (allele MM), DSS >2.84-13.75 (allele and antigen MM), DSS >13.75-19.39 (antigen MM), and DSS >19.39-36.62 (antigen MM). Using the lowest scoring quartile as the reference, the DSS groups were evaluated for associations with relapse, treatment-related mortality, acute and chronic graft-versus-host disease, leukemia-free survival, and overall survival in the entire cohort and also in subset analyses by disease and disease stage. No significant associations were found between DSS and any outcomes in the overall cohort using the quartile categories or treating DSS as a continuous variable. Higher DSS scores were associated with decreased engraftment in early-stage disease (P = .0003), but not in other disease stages. In summary, DSS does not correlate with transplantation outcomes, and the HistoCheck scoring system does not provide an effective technique for ranking HLA class I MM. The dataset used in this study is available to evaluate new algorithms proposed for donor selection.

摘要

目前,尚无可靠的评分系统可用于预测在没有与 HLA 等位基因匹配供体的情况下,应选择哪些 HLA 错配(MM)无关供体。我们评估了 MM 分级系统 HistoCheck 在预测 HLA Ⅰ类错配相关风险方面的能力,该系统评估了 744 名接受单等位基因或抗原 HLA-A、-B 或 -C MM 清髓性无关供体造血干细胞移植的急性髓系白血病、急性淋巴细胞白血病、慢性髓系白血病或骨髓增生异常综合征患者的风险,这些患者通过国家骨髓供者计划在 1988 年至 2003 年间进行移植。使用多变量模型调整其他重要临床危险因素。使用 HistoCheck 基于网络的工具对 HLA MM 进行评分,并将患者分为 4 个四分位组:差异评分(DSS)1.04-2.84(等位基因 MM)、DSS>2.84-13.75(等位基因和抗原 MM)、DSS>13.75-19.39(抗原 MM)和 DSS>19.39-36.62(抗原 MM)。以评分最低的四分位数为参照,评估 DSS 组与整个队列中疾病复发、治疗相关死亡率、急性和慢性移植物抗宿主病、无白血病生存率和总生存率的关系,也通过疾病和疾病分期进行亚组分析。在整个队列中,使用四分位类别或连续变量处理 DSS 时,均未发现 DSS 与任何结果之间存在显著关联。较高的 DSS 评分与早期疾病中的植入减少相关(P =.0003),但在其他疾病阶段则不然。总之,DSS 与移植结果不相关,HistoCheck 评分系统并不能为 HLA Ⅰ类 MM 分级提供有效的技术。本研究使用的数据集可用于评估新提出的用于供体选择的算法。

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