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完成乐卫玛预防治疗后发生迟发性巨细胞病毒感染的危险因素。

Risk factors for late cytomegalovirus infection after completing letermovir prophylaxis.

机构信息

Department of Medicine and Biosystemic Science, Kyushu University Graduate School of Medical Science, 3-1-1, Maidashi, Higashi-ku, Fukuoka, 812-8582, Japan.

Department of Hematology, Clinical Immunology, and Infectious Diseases, Ehime University Graduate School of Medicine, Ehime, Japan.

出版信息

Int J Hematol. 2022 Aug;116(2):258-265. doi: 10.1007/s12185-022-03348-2. Epub 2022 May 6.

DOI:10.1007/s12185-022-03348-2
PMID:35524024
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.

摘要

预防性使用来特莫韦(LMV)可显著降低异基因造血细胞移植(allo-HCT)后 100 天内早期临床显著巨细胞病毒(csCMV)感染的发生率,从而改善移植结果。然而,一些患者在完成 LMV 预防后最终会发展为晚期 csCMV 感染(超过第 100 天)。为了评估晚期 csCMV 感染的发生率及其危险因素和对移植结果的影响,对 81 名未在 LMV 预防期间发生早期 csCMV 感染的 allo-HCT 受者进行了回顾性分析。其中,23 名(28.4%)患者在移植后中位数 131 天(即在 LMV 停药后 30 天)发生晚期 csCMV 感染(直至第 180 天)。晚期 csCMV 感染与明显延迟的免疫重建有关:来自 HLA 错配供体(风险比[HR] = 13.0,p = 0.011)或 CMV-IgG 阴性供体(HR = 2.39,p = 0.043)的患者发生感染的风险显著更高。在这项研究中,具有和不具有晚期 csCMV 感染的患者之间的移植结果没有差异。这表明需要在更多的 allo-HCT 受者中,特别是在具有“高危”供体的受者中,明确延长 LMV 给药预防晚期 csCMV 感染的疗效。

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本文引用的文献

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Transpl Infect Dis. 2021 Apr;23(2):e13487. doi: 10.1111/tid.13487. Epub 2020 Oct 27.
2
Haploidentical allogeneic hematopoietic stem cell transplantation increases the risk of cytomegalovirus infection in adult patients with acute leukemia.单倍体相合异基因造血干细胞移植增加了成年急性白血病患者巨细胞病毒感染的风险。
Transpl Infect Dis. 2019 Aug;21(4):e13096. doi: 10.1111/tid.13096. Epub 2019 May 11.
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Risk factors for the development of cytomegalovirus disease after allogeneic stem cell transplantation.
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Blood Adv. 2024 Mar 12;8(5):1084-1093. doi: 10.1182/bloodadvances.2023010735.
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Blood Sci. 2024 Jan 10;6(1):e00178. doi: 10.1097/BS9.0000000000000178. eCollection 2024 Jan.
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