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Early cytomegalovirus reactivation remains associated with increased transplant-related mortality in the current era: a CIBMTR analysis

机译:CIBMTR分析表明在当前时代早期巨细胞病毒的重新活化仍与移植相关的死亡率增加相关

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摘要

Single-center studies have reported an association between early (before day 100) cytomegalovirus (CMV) reactivation and decreased incidence of relapse for acute myeloid leukemia (AML) following allogeneic hematopoietic cell transplantation. To substantiate these preliminary findings, the Center for International Blood and Marrow Transplant Research (CIBMTR) Database was interrogated to analyze the impact of CMV reactivation on hematologic disease relapse in the current era. Data from 9469 patients transplanted with bone marrow or peripheral blood between 2003 and 2010 were analyzed according to 4 disease categories: AML (n = 5310); acute lymphoblastic leukemia (ALL, n = 1883); chronic myeloid leukemia (CML, n = 1079); and myelodysplastic syndrome (MDS, n = 1197). Median time to initial CMV reactivation was 41 days (range, 1-362 days). CMV reactivation had no preventive effect on hematologic disease relapse irrespective of diagnosis. Moreover, CMV reactivation was associated with higher nonrelapse mortality [relative risk [RR] among disease categories ranged from 1.61 to 1.95 and P values from .0002 to <.0001; 95% confidence interval [CI], 1.14-2.61). As a result, CMV reactivation was associated with lower overall survival for AML (RR = 1.27; 95% CI, 1.17-1.38; P <.0001), ALL (RR = 1.46; 95% CI, 1.25-1.71; P <.0001), CML (RR = 1.49; 95% CI, 1.19-1.88; P = .0005), and MDS (RR = 1.31; 95% CI, 1.09-1.57; P = .003). In conclusion, CMV reactivation continues to remain a risk factor for poor posttransplant outcomes and does not seem to confer protection against hematologic disease relapse.
机译:单中心研究报告了早期(第100天之前)巨细胞病毒(CMV)激活与同种异体造血细胞移植后急性髓细胞性白血病(AML)复发率降低之间的相关性。为了证实这些初步发现,对国际血液和骨髓移植研究中心(CIBMTR)数据库进行了研究,以分析CMV激活对当前时代血液病复发的影响。根据4种疾病类别分析了2003年至2010年间9469例骨髓或外周血移植患者的数据:AML(n = 5310);急性淋巴细胞白血病(ALL,n = 1883);慢性粒细胞白血病(CML,n = 1079);和骨髓增生异常综合症(MDS,n = 1197)。初始CMV重新激活的中位时间为41天(范围1-362天)。无论诊断如何,CMV的活化对血液系统疾病的复发均无预防作用。此外,CMV的重新激活与较高的非复发死亡率[相对风险[RR]]相关,疾病类别为1.61至1.95,P值为.0002至<.0001; 95%置信区间[CI],1.14-2.61)。结果,CMV的重新激活与AML的总生存期较低(RR = 1.27; 95%CI,1.17-1.38; P <.0001),ALL(RR = 1.46; 95%CI,1.25-1.71; P <。 0001),CML(RR = 1.49; 95%CI,1.19-1.88; P = .0005)和MDS(RR = 1.31; 95%CI,1.09-1.57; P = .003)。总而言之,CMV的再激活仍然是移植后预后不良的危险因素,并且似乎并未提供针对血液学疾病复发的保护作用。

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