National Clinical Research Center for Hematologic Diseases, the First Affiliated Hospital of Soochow University, Suzhou, 215006, Jiangsu, China.
Jiangsu Institute of Hematology, Institute of Blood and Marrow Transplantation, Collaborative Innovation Center of Hematology, Soochow University, Suzhou, 215006, Jiangsu, China.
J Hematol Oncol. 2024 Oct 12;17(1):94. doi: 10.1186/s13045-024-01612-y.
Letermovir (LTV) prophylaxis is effective in reducing the incidence of clinically significant cytomegalovirus (CMV) infection (cs CMVi) after allogeneic haematopoietic stem cell transplantation (allo-HSCT). Since our centre began administering LTV prophylaxis in June 2022, we have observed a certain increase in the incidence of Epstein-Barr virus (EBV) reactivation after haploidentical HSCT. We retrospectively analysed 230 consecutive patients who underwent haploidentical HSCT with rabbit anti-thymocyte globulin (ATG) from October 2022 to June 2023. The LTV group included 133 patients who received LTV prophylaxis, and the control group included 97 patients who did not receive LTV prophylaxis. At 1 year after HSCT, EBV reactivation was observed in 36 patients (27%) in the LTV group and 13 patients (13%) in the control group (p = 0.012). All patients with EBV reactivation had EBV-DNAemia, and one patient in each group developed EBV-associated posttransplantation lymphoproliferative disorder (PTLD). The proportion of patients with low EBV-DNA loads (> 5 × 10 to < 1 × 10 copies/mL) was greater in the LTV group than in the control group (23% vs. 10%, p = 0.01). The proportion of patients with CMV reactivation was lower in the LTV group than in the control group (35% vs. 56%, p = 0.002). There was no significant difference between the groups in terms of neutrophil and platelet count recovery, the cumulative incidence of acute/chronic graft-versus-host disease, overall survival, cumulative relapse rate or nonrelapse mortality. Our results show that the increased incidence of EBV reactivation may be associated with LTV prophylaxis for CMV after haploidentical HSCT.
来特莫韦(LTV)预防可有效降低异基因造血干细胞移植(allo-HSCT)后巨细胞病毒(CMV)感染的发生率。自我们中心于 2022 年 6 月开始使用 LTV 预防以来,我们观察到亲缘单倍体 HSCT 后 EBV 再激活的发生率有所增加。我们回顾性分析了 2022 年 10 月至 2023 年 6 月期间接受兔抗胸腺细胞球蛋白(ATG)治疗的 230 例连续亲缘单倍体 HSCT 患者。LTV 组包括 133 例接受 LTV 预防的患者,对照组包括 97 例未接受 LTV 预防的患者。HSCT 后 1 年,LTV 组有 36 例(27%)出现 EBV 再激活,对照组有 13 例(13%)出现 EBV 再激活(p=0.012)。所有 EBV 再激活患者均出现 EBV-DNA 血症,两组各有 1 例患者出现 EBV 相关移植后淋巴组织增生性疾病(PTLD)。LTV 组 EBV-DNA 载量低(>5×10 至 <1×10 拷贝/mL)的患者比例高于对照组(23% vs. 10%,p=0.01)。LTV 组 CMV 再激活的患者比例低于对照组(35% vs. 56%,p=0.002)。两组间中性粒细胞和血小板计数恢复、急性/慢性移植物抗宿主病累积发生率、总生存率、累积复发率或非复发死亡率无显著差异。我们的结果表明,亲缘单倍体 HSCT 后 LTV 预防 CMV 可能与 EBV 再激活发生率增加有关。