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来自匹配相关供体的异基因造血干细胞移植后晚期感染的危险因素。

Risk factors for late infections after allogeneic hematopoietic stem cell transplantation from a matched related donor.

作者信息

Robin Marie, Porcher Raphaël, De Castro Araujo Renato, de Latour Régis Peffault, Devergie Agnès, Rocha Vanderson, Larghero Jérome, Adès Lionel, Ribaud Patricia, Mary Jean-Yves, Socié Gérard

机构信息

Service d'Hématologie, Greffe Hôpital Saint Louis, Paris, France.

出版信息

Biol Blood Marrow Transplant. 2007 Nov;13(11):1304-12. doi: 10.1016/j.bbmt.2007.07.007. Epub 2007 Sep 7.

Abstract

After allogeneic hematopoietic stem cell transplantation (HSCT), early infections represent a major cause of morbidity and mortality but little information has been previously reported on late infections. Late infection incidence and risk factors were retrospectively determined in 196 long-term survivors after HLA matched related HSCT. Patients transplanted for aplastic anemia, chronic myelogenous leukemia (CML), and acute myelogenous leukemia (AML) were included. Median follow-up was 8 years. Thirty patients died beyond the first year, causes of death were relapse (n = 10) and infections (n = 19, associated with graft-versus-host disease [GVHD] in 16 patients). Late severe bacterial (LSB) and fungal infections occurred in 30 and 8 patients, yielding to an 8-year cumulative incidence of 15 (95%CI: 10-20) and 4% (95%CI: 1-6), respectively. The majority of viral infections were hepatitis C (HCV) and VZV (8-year cumulative incidence: 10 (95%CI: 5-14) and 27% (95%CI: 20-34), respectively. Three risk factors for LSB have been identified in multiple Cox analysis: CMV status (positive recipient and negative donor) (hazard ratio [HR]: 2.5, 95%CI: 1.1-5.9, P = .033), irradiation-based conditioning regimen (HR: 3.1, 95%CI: 1.2-7.8, P = .016), and extensive chronic GVHD (cGVHD; HR: 2.9, 95%CI: 1.3-6.9, P = .013). Extensive cGVHD was the only risk factor for non-HCV viral infections in patients transplanted for AML or CML (HR: 2.7, 95%CI: 1.4-5.1, P = .002). After HSCT, patients remain at high risk of infections even late after transplantation, in particular, with the above risk factors, and required a prolonged follow-up.

摘要

在异基因造血干细胞移植(HSCT)后,早期感染是发病和死亡的主要原因,但此前关于晚期感染的报道较少。我们对196例HLA配型相合的亲缘HSCT长期存活者的晚期感染发生率及危险因素进行了回顾性研究。纳入因再生障碍性贫血、慢性粒细胞白血病(CML)和急性髓细胞白血病(AML)接受移植的患者。中位随访时间为8年。30例患者在第1年后死亡,死亡原因包括复发(n = 10)和感染(n = 19,其中16例与移植物抗宿主病[GVHD]相关)。30例和8例患者分别发生了晚期严重细菌(LSB)和真菌感染,8年累积发生率分别为15%(95%CI:10 - 20)和4%(95%CI:1 - 6)。大多数病毒感染为丙型肝炎病毒(HCV)和水痘带状疱疹病毒(VZV)(8年累积发生率分别为10%(95%CI:5 - 14)和27%(95%CI:20 - 34))。在多因素Cox分析中确定了LSB的三个危险因素:巨细胞病毒(CMV)状态(受者阳性而供者阴性)(风险比[HR]:2.5,95%CI:1.1 - 5.9,P = 0.033)、基于放疗的预处理方案(HR:3.1,95%CI:1.2 - 7.8,P = 0.016)和广泛慢性GVHD(cGVHD;HR:2.9,95%CI:1.3 - 6.9,P = 0.013)。广泛cGVHD是AML或CML移植患者非HCV病毒感染的唯一危险因素(HR:2.7,95%CI:1.4 - 5.1,P = 0.002)。HSCT后,患者即使在移植后期仍有较高的感染风险,尤其是存在上述危险因素时,需要延长随访时间。

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