医学
累积发病率
入射(几何)
巨细胞病毒
祖细胞
内科学
造血干细胞移植
胃肠病学
干细胞
贝塔赫佩斯病毒科
移植
免疫学
疱疹病毒科
病毒性疾病
病毒
物理
光学
生物
遗传学
作者
Carlos Solano,Estela Giménez,Eliseo Albert,Eva M. Mateo,Mercedes Gómez,Rosa Goterris,Ariadna Pérez,Paula Amat,Juan Carlos Hernández‐Boluda,Marc Poch,José Luís Piñana,David Navarro
标识
DOI:10.1038/s41409-018-0251-0
摘要
To gauge the risk of delaying initiation of prophylaxis with letermovir from the time of donor infusion to prevent CMV infection in allo-HSCT recipients we investigated the clinical outcomes of CMV DNAemia episodes occurring before engraftment, and compared to that of episodes developing after engraftment (up to day +365). A total of 197 consecutive adult patients were included. Plasma CMV DNA load was monitored by real-time PCR assays [limit of detection: 31 IU/ml]. A total of 150 out of 197 patients had CMV DNAemia (cumulative incidence of 77%; 95% CI, 73–81%), and 38 out of the 197 patients developed it before engraftment (cumulative incidence, 19%; 95% CI, 10–30.3%). Nine episodes of CMV DNAemia were detected prior to the time of donor progenitor cell infusion. A greater number of post-engraftment episodes required preemptive antiviral therapy compared with pre-engraftment episodes (62.5% vs 44.7%; P = 0.05). The cellular content of the donor progenitor cell infusion and transplant characteristics of patients did not differ between patients with pre-engraftment or post-engraftment CMV DNAemia. The cumulative incidence of overall mortality by days 100 and 365, aGvHD by day 100 and relapse by day 365 were not significantly different between patients with pre-engraftment or post-engraftment CMV DNAemia.
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