Cohen L, Yeshurun M, Shpilberg O, Ram R
Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
BMT Unit, Davidoff Cancer Center, Beilinson Hospital, Petah Tikva, Israel.
Transpl Infect Dis. 2015 Aug;17(4):510-7. doi: 10.1111/tid.12398. Epub 2015 Jun 18.
We aimed to study the risk factors for first and subsequent cytomegalovirus (CMV) infection among patients who are CMV seropositive and underwent allogeneic hematopoietic cell transplantation (HCT).
We performed an historical cohort study of all sequential CMV-seropositive patients who underwent allogeneic HCT at a single center. Between May 2007 and December 2012, 121 patients fulfilled inclusion criteria.
Multivariate model identified myeloablative preparative regimen (hazard ratio [HR] = 4.297, P = 0.033) and acute graft-versus-host disease (GVHD) prior to infection (HR = 5.091, P = 0.021) as risk factors for first CMV infection. The cumulative incidences of first CMV infection for patients with 0, 1, and 2 risk factors were 52%, 71%, and 91%, respectively. Multivariate analysis identified the diagnosis of lymphoma/myeloma (HR = 3.5, P = 0.049) and GVHD (HR = 1.280, P = 0.045) as risk factors for subsequent CMV infection. High graft CD3 stem cell dose was associated with a trend of lower rate of subsequent CMV infection (HR = 0.543, P = 0.056). The cumulative incidences for subsequent CMV infection in patients with 0, 1, and 2-3 risk factors were 11%, 41%, and 77%, respectively.
In conclusion, in CMV-seropositive patients, myeloablative conditioning and acute GVHD are risk factors for first CMV infection, while lymphoma/myeloma, ongoing GVHD, and low CD3 graft content are risk factors for subsequent infection.
我们旨在研究巨细胞病毒(CMV)血清学阳性且接受异基因造血细胞移植(HCT)的患者首次及后续CMV感染的危险因素。
我们对在单一中心接受异基因HCT的所有连续性CMV血清学阳性患者进行了一项历史性队列研究。2007年5月至2012年12月期间,121例患者符合纳入标准。
多变量模型确定清髓性预处理方案(风险比[HR]=4.297,P=0.033)和感染前的急性移植物抗宿主病(GVHD)(HR=5.091,P=0.021)为首次CMV感染的危险因素。具有0、1和2个危险因素的患者首次CMV感染的累积发生率分别为52%、71%和91%。多变量分析确定淋巴瘤/骨髓瘤的诊断(HR=3.5,P=0.049)和GVHD(HR=1.280,P=0.045)为后续CMV感染的危险因素。高移植CD3干细胞剂量与后续CMV感染率较低的趋势相关(HR=0.543,P=0.056)。具有0、1和2 - 3个危险因素的患者后续CMV感染的累积发生率分别为11%、41%和77%。
总之,在CMV血清学阳性患者中,清髓性预处理和急性GVHD是首次CMV感染的危险因素,而淋巴瘤/骨髓瘤、持续性GVHD和低CD3移植物含量是后续感染的危险因素。