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异基因造血干细胞移植后难治性巨细胞病毒(CMV)感染的患者存在 CMV 疾病和非复发死亡率高的风险。

Patients with refractory cytomegalovirus (CMV) infection following allogeneic haematopoietic stem cell transplantation are at high risk for CMV disease and non-relapse mortality.

机构信息

Peking University People's Hospital, Institute of Haematology, Beijing Key Laboratory of HSCT, Beijing, China.

Peking University People's Hospital, Institute of Haematology, Beijing Key Laboratory of HSCT, Beijing, China.

出版信息

Clin Microbiol Infect. 2015 Dec;21(12):1121.e9-15. doi: 10.1016/j.cmi.2015.06.009. Epub 2015 Jun 17.

DOI:10.1016/j.cmi.2015.06.009
PMID:26093077
Abstract

Pre-emptive therapy is an effective approach for cytomegalovirus (CMV) control; however, refractory CMV still occurs in a considerable group of recipients after allogeneic haematopoietic stem cell transplantation (allo-HSCT). Until now, hardly any data have been available about the clinical characteristics and risk factors of refractory CMV, or its potential harmful impact on the clinical outcome following allo-HSCT. We studied transplant factors affecting refractory CMV in the 100 days after allo-HSCT, and the impact of refractory CMV on the risk of CMV disease and non-relapse mortality (NRM). We retrospectively studied 488 consecutive patients with CMV infection after allo-HSCT. Patients with refractory CMV in the 100 days after allo-HSCT had a higher incidence of CMV disease and NRM than those without refractory CMV (11.9% vs. 0.8% and 17.1% vs. 8.3%, respectively). Multivariate analysis showed that refractory CMV infection in the 100 days after allo-HSCT was an independent risk factor for CMV disease (hazard ratio (HR) 10.539, 95% CI 2.467-45.015, p 0.001), and that refractory CMV infection within 60-100 days after allo-HSCT was an independent risk factor for NRM (HR 8.435, 95% CI 1.511-47.099, p 0.015). Clinical factors impacting on the risk of refractory CMV infection included receiving transplants from human leukocyte antigen-mismatched family donors (HR 2.012, 95% CI 1.603-2.546, p <0.001) and acute graft-versus-host disease (HR 1.905, 95% CI 1.352-2.686, p <0.001). We conclude that patients with refractory CMV infection during the early stage after allo-HSCT are at high risk for both CMV disease and NRM.

摘要

preemptive 治疗是控制巨细胞病毒(CMV)的有效方法;然而,异基因造血干细胞移植(allo-HSCT)后,相当一部分受者仍存在难治性 CMV。到目前为止,几乎没有关于难治性 CMV 的临床特征和危险因素的数据,也没有关于其对 allo-HSCT 后临床结果的潜在有害影响的数据。我们研究了移植因素对 allo-HSCT 后 100 天内难治性 CMV 的影响,以及难治性 CMV 对 CMV 疾病和非复发死亡率(NRM)风险的影响。我们回顾性研究了 488 例 allo-HSCT 后 CMV 感染患者。allo-HSCT 后 100 天内发生难治性 CMV 的患者 CMV 疾病和 NRM 的发生率高于未发生难治性 CMV 的患者(11.9%比 0.8%和 17.1%比 8.3%)。多变量分析显示,allo-HSCT 后 100 天内难治性 CMV 感染是 CMV 疾病的独立危险因素(风险比(HR)10.539,95%置信区间 2.467-45.015,p<0.001),allo-HSCT 后 60-100 天内难治性 CMV 感染是 NRM 的独立危险因素(HR 8.435,95%置信区间 1.511-47.099,p=0.015)。影响难治性 CMV 感染风险的临床因素包括接受 HLA 配型不合的家族供者移植(HR 2.012,95%置信区间 1.603-2.546,p<0.001)和急性移植物抗宿主病(HR 1.905,95%置信区间 1.352-2.686,p<0.001)。我们得出结论,allo-HSCT 后早期发生难治性 CMV 感染的患者 CMV 疾病和 NRM 的风险均较高。

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