Department of Pediatrics, Division of Blood and Marrow Transplantation, University of Minnesota, Minneapolis, Minnesota 55455, USA.
Biol Blood Marrow Transplant. 2010 Feb;16(2):215-22. doi: 10.1016/j.bbmt.2009.09.019. Epub 2009 Sep 26.
This study investigated the impact of pretransplant cytomegalovirus (CMV) serostatus and posttransplant CMV reactivation and disease on umbilical cord blood transplant (UCBT) outcomes. Between 1994 and 2007, 332 patients with hematologic malignancies underwent UCBT and 54% were CMV seropositive. Pretransplant recipient CMV serostatus had no impact on acute or chronic graft-versus-host disease (aGVHD, cGVHD), relapse, disease-free survival (DFS), or overall survival (OS). There was a trend toward greater day 100 treatment-related mortality (TRM) in CMV-seropositive recipients (P=.07). CMV reactivation occurred in 51% (92/180) of patients with no difference in myeloablative (MA) versus reduced-intensity conditioning (RIC) recipients (P=.33). Similarly, reactivation was not influenced by the number of UCB units transplanted, the degree of HLA disparity, the CD34(+) or CD3(+) cell dose, or donor killer cell immunoglobulin-like receptor (KIR) gene haplotype. Rapid lymphocyte recovery was associated with CMV reactivation (P=.02). CMV reactivation was not associated with aGVHD (P=.97) or cGVHD (P=.65), nor did it impact TRM (P=.88), relapse (P=.62), or survival (P=.78). CMV disease occurred in 13.8% of the CMV-seropositive patients, resulting in higher TRM (P=.01) and lower OS (P=.02). Thus, although recipient CMV serostatus and CMV reactivation have little demonstrable impact on UCB transplant outcomes, the development of CMV disease remains a risk, associated with inferior outcomes.
本研究调查了移植前巨细胞病毒(CMV)血清状态和移植后 CMV 再激活及疾病对脐血移植(UCBT)结果的影响。1994 年至 2007 年间,332 例血液系统恶性肿瘤患者接受了 UCBT,其中 54%为 CMV 血清阳性。移植前受者 CMV 血清状态对急性或慢性移植物抗宿主病(aGVHD、cGVHD)、复发、无病生存(DFS)或总生存(OS)均无影响。CMV 血清阳性受者第 100 天治疗相关死亡率(TRM)较高(P=.07)。92/180 例患者发生 CMV 再激活,骨髓清除性(MA)与减低强度预处理(RIC)受者之间无差异(P=.33)。同样,再激活与移植的 UCBT 单位数量、HLA 错配程度、CD34+或 CD3+细胞剂量或供者杀伤细胞免疫球蛋白样受体(KIR)基因单倍型无关。快速淋巴细胞恢复与 CMV 再激活相关(P=.02)。CMV 再激活与 aGVHD(P=.97)或 cGVHD(P=.65)无关,也不影响 TRM(P=.88)、复发(P=.62)或生存(P=.78)。13.8%的 CMV 血清阳性患者发生 CMV 病,导致 TRM 较高(P=.01)和 OS 较低(P=.02)。因此,尽管受者 CMV 血清状态和 CMV 再激活对 UCBT 结果的影响不大,但 CMV 病的发生仍然是一个风险,与不良结局相关。