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异基因造血干细胞移植后骨髓增生异常综合征中 EBV 再激活的发生率、危险因素及临床意义。

Incidence, risk factors, and clinical significance of Epstein-Barr virus reactivation in myelodysplastic syndrome after allogeneic haematopoietic stem cell transplantation.

机构信息

Jiangsu Institute of Haematology, The First Affiliated Hospital of Soochow University, Suzhou, China.

Institute of Blood and Marrow Transplantation, Suzhou, China.

出版信息

Ann Hematol. 2019 Apr;98(4):987-996. doi: 10.1007/s00277-019-03603-3. Epub 2019 Feb 4.

DOI:10.1007/s00277-019-03603-3
PMID:30715567
Abstract

Epstein-Barr virus (EBV) reactivation is a life-threatening complication after allogeneic haematopoietic stem cell transplantation (allo-HSCT). In this study, we investigated the characteristics of EBV reactivation in 186 consecutive myelodysplastic (MDS) patients who underwent allo-HSCT in our centre. In 35 patients (18.8%) who experienced EBV reactivation after allo-HSCT, the median onset was 53 days (range 4-381 days). The cumulative incidence of EBV reactivation at the first, sixth, and twelfth month after allo-HSCT was 10.7%, 15.1%, and 17.9%, respectively. Twenty-five patients (71.4%) received pre-emptive rituximab therapy, and no patients developed post-transplant lymphoproliferative disorders. Stem cell source was proven to be a risk factor correlated with EBV reactivation. The cumulative incidence of relapse in the EBV-positive group was 11.4%, 25.2%, and 31.0% at the first, second, and third year after transplantation, respectively, being significantly higher than the corresponding 6.8%, 10.2%, and 10.2%, in the EBV-negative group (P = 0.014). Prognostic analysis showed that EBV reactivation was an independent risk factor for relapse-free survival (RFS). Patients in the EBV-positive group showed obviously shorter RFS than those in the EBV-negative group, with 3-year RFS of 62% and 85%, respectively (P = 0.017).

摘要

背景:异基因造血干细胞移植(allo-HSCT)后,EB 病毒(EBV)再激活是一种危及生命的并发症。本研究旨在探讨我们中心接受 allo-HSCT 的 186 例骨髓增生异常(MDS)患者 EBV 再激活的特点。

方法:在 35 例 allo-HSCT 后发生 EBV 再激活的患者中,中位发病时间为 53 天(4-381 天)。allo-HSCT 后第 1、6 和 12 个月 EBV 再激活的累积发生率分别为 10.7%、15.1%和 17.9%。25 例(71.4%)患者接受了抢先利妥昔单抗治疗,无患者发生移植后淋巴组织增生性疾病。

结果:干细胞来源被证明是与 EBV 再激活相关的危险因素。在 EBV 阳性组中,移植后第 1、2 和 3 年的复发累积发生率分别为 11.4%、25.2%和 31.0%,显著高于 EBV 阴性组的 6.8%、10.2%和 10.2%(P=0.014)。预后分析显示 EBV 再激活是无复发生存(RFS)的独立危险因素。

结论:EBV 再激活患者的 RFS 明显短于 EBV 阴性患者,3 年 RFS 分别为 62%和 85%(P=0.017)。

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