Risk factors for late cytomegalovirus infection after completing letermovir prophylaxis

被引:18
作者
Mori, Yasuo [1 ]
Harada, Takuya [1 ]
Yoshimoto, Goichi [1 ]
Shima, Takahiro [1 ]
Numata, Akihiko [1 ]
Jinnouchi, Fumiaki [1 ]
Yamauchi, Takuji [1 ]
Kikushige, Yoshikane [1 ]
Kunisaki, Yuya [1 ]
Kato, Koji [1 ]
Takenaka, Katsuto [1 ,2 ]
Akashi, Koichi [1 ]
Miyamoto, Toshihiro [1 ]
机构
[1] Kyushu Univ, Dept Med & Biosyst Sci, Grad Sch Med Sci, Higashi Ku, 3-1-1 Maidashi, Fukuoka 8128582, Japan
[2] Ehime Univ, Dept Hematol Clin Immunol & Infect Dis, Grad Sch Med, Matsuyama, Ehime, Japan
关键词
Letermovir; Cytomegalovirus; Prophylaxis; Late-onset reactivation; Allogeneic hematopoietic cell transplantation; STEM-CELL TRANSPLANTATION; UMBILICAL-CORD BLOOD; IMMUNE RECONSTITUTION; T-CELLS; DISEASE; RECOVERY; REACTIVATION; RECIPIENTS; MORTALITY; LEUKEMIA;
D O I
10.1007/s12185-022-03348-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
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.
引用
收藏
页码:258 / 265
页数:8
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