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停药后迟发性巨细胞病毒感染在脐血移植受者中很常见。

Delayed-onset cytomegalovirus infection is frequent after discontinuing letermovir in cord blood transplant recipients.

机构信息

Department of Medicine, University of Washington, Seattle, WA.

Vaccine and Infectious Disease Division, and.

出版信息

Blood Adv. 2021 Aug 24;5(16):3113-3119. doi: 10.1182/bloodadvances.2021004362.

Abstract

Cytomegalovirus (CMV)-seropositive umbilical cord blood transplantation (CBT) recipients have a high incidence of CMV-associated complications. There are limited data regarding the efficacy of letermovir for preventing clinically significant CMV infection (CS-CMVi), and the impact of letermovir prophylaxis on delayed-onset CMV reactivation after letermovir discontinuation, in CBT recipients. We compared the cumulative incidence of CS-CMVi and CMV detection in 21 CMV-seropositive CBT recipients receiving letermovir prophylaxis with a historical cohort of 40 CBT recipients receiving high-dose valacyclovir prophylaxis. Letermovir was administered on day +1 up to day +98. The cumulative incidence of CS-CMVi was significantly lower by day 98 in the letermovir cohort (19% vs 65%). This difference was lost by 1 year due to a higher incidence of delayed-onset CMV reactivation in the letermovir cohort. No patients developed CMV disease in the letermovir cohort within the first 98 days compared with 2 cases (2.4%) in the high-dose valacyclovir cohort; 2 patients developed CMV enteritis after discontinuing letermovir. Median viral loads were similar in both cohorts. Thus, letermovir is effective at preventing CS-CMVi after CBT, but frequent delayed-onset infections after letermovir discontinuation mandate close monitoring and consideration for extended prophylaxis.

摘要

巨细胞病毒(CMV)-阳性脐带血移植(CBT)受者CMV 相关并发症发生率高。关于来特莫韦预防临床显著 CMV 感染(CS-CMVi)的疗效,以及来特莫韦停药后延迟性 CMV 再激活的发生率,在 CBT 受者中的数据有限。我们比较了 21 例 CMV 阳性 CBT 受者接受来特莫韦预防与 40 例接受高剂量伐昔洛韦预防的历史队列中 CS-CMVi 和 CMV 检测的累积发生率。来特莫韦于+1 天至+98 天给药。来特莫韦组的 CS-CMVi 累积发生率在第 98 天显著降低(19% vs 65%)。由于来特莫韦组延迟性 CMV 再激活发生率较高,这一差异在 1 年内消失。来特莫韦组在 98 天内无患者发生 CMV 病,而高剂量伐昔洛韦组有 2 例(2.4%);2 例患者在停用来特莫韦后发生 CMV 肠炎。两组的病毒载量中位数相似。因此,来特莫韦在 CBT 后有效预防 CS-CMVi,但来特莫韦停药后频繁发生延迟性感染,需要密切监测并考虑延长预防。

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