Faculty of Medicine, Université de Montréal, Montréal, QC H3T 1J4, Canada.
Department of Microbiology, Infectious Diseases and Immunology, Faculty of Medicine, Université de Montréal, Montréal, QC H3T 1J4, Canada.
Curr Oncol. 2024 May 14;31(5):2780-2795. doi: 10.3390/curroncol31050211.
Epstein-Barr virus-related post-transplantation lymphoproliferative disorder (EBV-PTLD) is a serious complication following hematopoietic stem cell transplantation (HSCT). A pre-emptive strategy using rituximab, which aims to manage patients early at the time of EBV reactivation to avoid PTLD, has been recommended by the most recent ECIL-6 guidelines in 2016. However, there is still a great heterogeneity of viral-load monitoring protocols, targeted patient populations, and pre-emptive treatment characteristics between centers, making precise EBV monitoring recommendations difficult. We conducted a literature review from the most recent publications between 1 January 2015 and 1 August 2023, to summarize the emerging data on EBV-PTLD prevention strategies in HSCT recipients, including the EBV-DNA threshold and use of rituximab. We also present the results of a survey of current practices carried out in 12 of the main HSCT centers across Canada. We confirm that pre-emptive rituximab remains an efficient strategy for EBV-PTLD prevention. However, there is an urgent need to perform prospective, randomized, multicentric trials with larger numbers of patients reflecting current practices to determine the best clinical conduct with regards to rituximab dosing, timing of treatment, and criteria to initiate treatments. Longer follow-ups will also be necessary to assess patients' long-term outcomes.
中文译文:
移植后 EBV 相关淋巴组织增生性疾病(EBV-PTLD)是造血干细胞移植(HSCT)后的严重并发症。2016 年,ECIL-6 指南推荐了一种抢先使用利妥昔单抗的策略,旨在 EBV 再激活时尽早管理患者,以避免 PTLD。然而,各中心之间在病毒载量监测方案、靶向患者人群和抢先治疗特征方面仍存在很大的异质性,使得难以精确监测 EBV。我们对 2015 年 1 月 1 日至 2023 年 8 月 1 日期间的最新出版物进行了文献综述,以总结 HSCT 受者中 EBV-PTLD 预防策略的最新数据,包括 EBV-DNA 阈值和利妥昔单抗的使用。我们还介绍了在加拿大 12 个主要 HSCT 中心进行的当前实践调查结果。我们确认抢先使用利妥昔单抗仍然是预防 EBV-PTLD 的有效策略。然而,迫切需要开展前瞻性、随机、多中心试验,纳入更多反映当前实践的患者,以确定利妥昔单抗剂量、治疗时机和开始治疗的标准方面的最佳临床方案。还需要进行更长时间的随访,以评估患者的长期结局。