Ochs L, Shu X O, Miller J, Enright H, Wagner J, Filipovich A, Miller W, Weisdorf D
Department of Medicine, University of Minnesota, Minneapolis, USA.
Blood. 1995 Nov 15;86(10):3979-86.
Infectious complications are a major cause of morbidity and mortality after allogeneic bone marrow transplantation (BMT). We have evaluated the incidence of late infections (beyond day +50) in recipients of related (RD) and unrelated donor (URD) allogeneic BMT, factors associated with increased risks of infection, and the impact of the late infections on survival. Between 1989 and 1991, 249 patients received an RD (n = 151) or URD (n = 98) allogeneic BMT at the University of Minnesota and all late infections were investigated. Three hundred sixty-seven late infectious events developed in 162 patients between 50 days and 2 years after BMT. The incidence of any late infection was greater in URD versus RD recipients (84.7% v 68.2%, respectively; P = .009). In multivariate analysis, advanced graft-versus-host disease (GVHD) was significantly associated with late infections. The effect of GVHD was apparent only in RD recipients (relative risk [RR], 2.29; P = .003), whereas URD recipients, with or without GVHD, had more late infections compared with RD recipients without GVHD. Multivariate analysis showed that late posttransplantation infections were the dominant independent factor associated with increased nonrelapse mortality (RR, 5.5; P = .0001), resulting in improved 3-year survival for RD versus URD recipients (49.9% +/- 8% v 34.4% +/- 10%; P = .004). In this study, we observed that late infections are more frequent in URD recipients, resulting in substantially higher nonrelapse mortality. This prolonged period of increased infectious risk in URD recipients suggests the need for aggressive surveillance and therapy of late infections and perhaps prolonged antibiotic prophylaxis for all URD BMT recipients.
感染性并发症是异基因骨髓移植(BMT)后发病和死亡的主要原因。我们评估了相关供体(RD)和无关供体(URD)异基因BMT受者中晚期感染(移植后+50天以后)的发生率、与感染风险增加相关的因素以及晚期感染对生存的影响。1989年至1991年期间,249例患者在明尼苏达大学接受了RD(n = 151)或URD(n = 98)异基因BMT,并对所有晚期感染进行了调查。162例患者在BMT后50天至2年期间发生了367次晚期感染事件。URD受者中任何晚期感染的发生率均高于RD受者(分别为84.7%和68.2%;P = .009)。多因素分析显示,重度移植物抗宿主病(GVHD)与晚期感染显著相关。GVHD的影响仅在RD受者中明显(相对风险[RR],2.29;P = .003),而与无GVHD的RD受者相比,有或无GVHD的URD受者晚期感染更多。多因素分析表明,移植后晚期感染是与非复发死亡率增加相关的主要独立因素(RR,5.5;P = .0001),导致RD受者的3年生存率高于URD受者(49.9%±8%对34.4%±10%;P = .004)。在本研究中,我们观察到URD受者中晚期感染更为频繁,导致非复发死亡率显著更高。URD受者感染风险增加的这段延长时间表明,需要对晚期感染进行积极监测和治疗,或许还需要对所有URD BMT受者延长抗生素预防时间。