| Literature DB >> 35524024 |
Yasuo Mori1, Takuya Harada1, Goichi Yoshimoto1, Takahiro Shima1, Akihiko Numata1, Fumiaki Jinnouchi1, Takuji Yamauchi1, Yoshikane Kikushige1, Yuya Kunisaki1, Koji Kato1, Katsuto Takenaka1,2, Koichi Akashi1, Toshihiro Miyamoto3.
Abstract
Prophylactic use of letermovir (LMV) markedly reduces the incidence of early clinically significant cytomegalovirus (csCMV) infection within the first 100 days after allogeneic hematopoietic cell transplantation (allo-HCT), which improves transplant outcomes. However, some patients eventually develop late-csCMV infection (beyond day 100) after completing LMV prophylaxis. To assess the incidence of late-csCMV infection as well as its risk factors and impacts on transplant outcome, a total of 81 allo-HCT recipients who had not developed early csCMV infection during LMV prophylaxis were retrospectively analyzed. Among them, 23 (28.4%) patients developed late-csCMV infection (until day 180) at a median time of 131 days after transplantation and 30 days after LMV discontinuation, respectively. Late-csCMV infection was correlated with apparent delayed immune reconstitution: patients transplanted from HLA-mismatched donors (hazard ratio [HR] = 13.0, p = 0.011) or CMV-IgG-negative donors (HR = 2.39, p = 0.043) had a significantly higher risk. In this study, transplant outcomes did not differ between patients with and without late-csCMV infection. This suggests a need to clarify the efficacy of extended administration of LMV for preventing late-csCMV infection in a larger number of allo-HCT recipients, especially those with "high-risk" donors.Entities:
Keywords: Allogeneic hematopoietic cell transplantation; Cytomegalovirus; Late-onset reactivation; Letermovir; Prophylaxis
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Year: 2022 PMID: 35524024 DOI: 10.1007/s12185-022-03348-2
Source DB: PubMed Journal: Int J Hematol ISSN: 0925-5710 Impact factor: 2.319