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有临床风险因素的患者早期血浆生物标志物升高预示着异基因造血干细胞移植后非复发死亡率增加。

Elevation of Early Plasma Biomarkers in Patients with Clinical Risk Factors Predicts Increased Nonrelapse Mortality after Allogeneic Hematopoietic Stem Cell Transplantation.

机构信息

First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.

First Department of Internal Medicine, Kansai Medical University, Osaka, Japan.

出版信息

Transplant Cell Ther. 2021 Aug;27(8):660.e1-660.e8. doi: 10.1016/j.jtct.2021.04.025. Epub 2021 May 12.

DOI:10.1016/j.jtct.2021.04.025
PMID:33989832
Abstract

Early prediction of nonrelapse mortality (NRM) in patients undergoing allogeneic hematopoietic stem cell transplantation (allo-HSCT) based on the results of laboratory tests is challenging. Thus, there is a need to evaluate biomarkers for prediction of NRM, a major problem that offsets the advantages of allo-HSCT. We tested the validity and efficacy of 2 plasma biomarkers, ST2 and Reg3α, based on the Mount Sinai Acute GVHD International Consortium (MAGIC) algorithm, for early prediction of NRM in Japanese patients who underwent allo-HSCT. We conducted a multicenter retrospective study to analyze the clinical data of 112 patients with hematopoietic malignancies who underwent allo-HSCT. Patient blood samples on day 7 after allo-HSCT were obtained from 6 hospitals. The plasma concentrations of ST2 and Reg3α were used to calculate a 6-month NRM risk score. Based on the scores determined in this study, we identified 64 low-risk patients and 48 high-risk patients for the 6-month NRM. The cumulative incidence of 6-month NRM was 29.2% in the high-risk group and 10.9% in the low-risk group (P < .05). The cumulative incidence of relapse mortality was similar in the high-risk and low-risk patients. The biomarker score was predictive in patients with an unrelated donor, an HLA-mismatched donor, high/very high Disease Risk Index, and Hematopoietic Cell Transplantation Comorbidity Index ≥1. Multivariate analysis identified high biomarker probability as a significant predictor of NRM. The MAGIC algorithm based on blood samples obtained at 7 days after allo-HSCT can identify individuals at high risk for NRM among patients with clinical risk factors for NRM in a Japanese cohort.

摘要

基于实验室检测结果预测异基因造血干细胞移植(allo-HSCT)患者的非复发死亡率(NRM)具有挑战性。因此,需要评估用于预测 NRM 的生物标志物,这是一个主要问题,它抵消了 allo-HSCT 的优势。我们基于西奈山急性移植物抗宿主病国际联盟(MAGIC)算法,测试了 2 种血浆生物标志物 ST2 和 Reg3α 的有效性和功效,以预测日本 allo-HSCT 患者的 NRM。我们进行了一项多中心回顾性研究,分析了 112 名接受 allo-HSCT 的血液系统恶性肿瘤患者的临床数据。从 6 家医院采集了 allo-HSCT 后第 7 天的患者血液样本。使用 ST2 和 Reg3α 的血浆浓度来计算 6 个月 NRM 风险评分。根据本研究确定的评分,我们确定了 6 个月 NRM 的低危患者 64 例和高危患者 48 例。高危组的 6 个月 NRM 累积发生率为 29.2%,低危组为 10.9%(P<0.05)。高危和低危患者的复发死亡率累积发生率相似。该生物标志物评分在无关供体、HLA 错配供体、高/极高疾病风险指数和造血细胞移植合并症指数≥1 的患者中具有预测性。多变量分析确定高生物标志物概率是 NRM 的显著预测因子。基于 allo-HSCT 后 7 天获得的血液样本的 MAGIC 算法可以识别日本队列中具有 NRM 临床危险因素的患者中 NRM 风险较高的个体。

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