Department of Medicine, University of Washington, Seattle, WA.
Vaccine and Infectious Disease Division, and.
Blood Adv. 2021 Aug 24;5(16):3113-3119. doi: 10.1182/bloodadvances.2021004362.
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.
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。