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在肾移植受者中,依维莫司与吗替麦考酚酯之间巨细胞病毒感染的发生率:三项临床试验的汇总分析。

Cytomegalovirus incidence between everolimus versus mycophenolate in de novo renal transplants: pooled analysis of three clinical trials.

机构信息

Washington University School of Medicine Barnes-Jewish Hospital, St. Louis, MO, USA.

出版信息

Am J Transplant. 2011 Nov;11(11):2453-62. doi: 10.1111/j.1600-6143.2011.03674.x. Epub 2011 Aug 3.

Abstract

Everolimus (EVR) in heart and renal transplant (RTx) recipients may be associated with a decreased incidence of cytomegalovirus (CMV). A detailed analysis of the association between EVR versus mycophenolic acid (MPA) and CMV events has not been reported. CMV data from 2004 de novo RTx recipients from three-randomized, prospective, EVR studies A2309 (N = 833), B201 (N = 588) and B251 (N = 583) were retrospectively analyzed to identify differences between two EVR dosing groups and MPA. EVR groups received 1.5 mg/day, or 3 mg/day with either standard (SD-CsA) or reduced dose cyclosporine (RD-CsA). Controls received MPA with SD-CsA. CMV prophylaxis was as per center practice. CMV incidence (infection/syndrome, disease, viremia) was captured per local center evaluations. Kaplan-Meier analyses demonstrated that freedom from CMV viremia and infection/syndrome was significantly greater for EVR versus MPA for recipients without CMV prophylaxis. Among recipients who received prophylaxis, freedom from viremia was greater for EVR 3.0 mg; freedom from infection/syndrome was greater for EVR 3.0 and 1.5 mg. Although freedom from organ involvement was numerically greater for EVR, it was not statistically significant. This analysis documents significant reductions in the incidence of CMV infection/syndrome and viremia in EVR-treated de novo RTx recipients, especially those who did not receive CMV prophylaxis versus MPA.

摘要

依维莫司(EVR)在心脏和肾脏移植(RTx)受者中可能与降低巨细胞病毒(CMV)的发生率有关。尚未报道 EVR 与霉酚酸(MPA)和 CMV 事件之间的关联的详细分析。回顾性分析了来自三个随机、前瞻性 EVR 研究 A2309(N=833)、B201(N=588)和 B251(N=583)的 2004 例初治 RTx 受者的 CMV 数据,以确定两种 EVR 剂量组与 MPA 之间的差异。EVR 组分别接受 1.5 毫克/天或 3 毫克/天,联合标准(SD-CsA)或低剂量环孢素(RD-CsA)。对照组接受 SD-CsA 联合 MPA。CMV 预防采用中心实践。CMV 发生率(感染/综合征、疾病、病毒血症)根据当地中心评估进行捕获。Kaplan-Meier 分析表明,对于未接受 CMV 预防的受者,EVR 组与 MPA 组相比,CMV 病毒血症和感染/综合征的无复发率显著更高。在接受预防治疗的受者中,EVR 3.0mg 的病毒血症无复发率更高;EVR 3.0 和 1.5mg 的感染/综合征无复发率更高。尽管 EVR 的器官受累无复发率在数值上更高,但无统计学意义。这项分析记录了 EVR 治疗的初治 RTx 受者中 CMV 感染/综合征和病毒血症发生率的显著降低,尤其是那些未接受 CMV 预防的受者。

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