a Department of Hematology and Oncology , Weill Cornell Medicine , New York , NY , USA.
b Transplantation-Oncology Infectious Diseases Program, Weill Cornell Medicine , New York , NY , USA.
Leuk Lymphoma. 2019 Jul;60(7):1693-1696. doi: 10.1080/10428194.2018.1543877. Epub 2019 Feb 10.
Epstein-Barr virus (EBV) reactivation and post-transplant lymphoproliferative disorders (PTLD) are common and potentially fatal complications after allogeneic transplantation with mismatched donors and T-cell depletion. Haplo-cord transplantation combines a mismatched UCB graft with third-party cells. Conditioning involves thymoglobulin. EBV reactivation and PTLD were common in initial patients. As of March 2017, we administered a prophylactic dose of rituximab 375 mg/m pre-transplant. Among 147 patients who did not receive rituximab, the cumulative incidence of post-transplant EBV reactivation and of EBV PTLD was 13% and 8%, respectively. Among 51 who received pre-transplant rituximab, the incidences were 2% ( = .0017) and 0% ( = .04), respectively. There was no difference in time to hematopoietic recovery, in the incidence of CMV reactivation, of invasive blood stream infections or of proven or probable invasive fungal infections. Pre-transplant administration of rituximab is an effective and nontoxic intervention that drastically reduces EBV reactivation and PTLD in high-risk patients.
爱泼斯坦-巴尔病毒(EBV)再激活和移植后淋巴增殖性疾病(PTLD)是异基因移植和 T 细胞耗竭后与错配供体相关的常见且潜在致命的并发症。单倍体脐带血移植将错配的 UCB 移植物与第三方细胞相结合。预处理方案包括胸腺球蛋白。在最初的患者中,EBV 再激活和 PTLD 很常见。截至 2017 年 3 月,我们在移植前预防性给予利妥昔单抗 375mg/m2。在未接受利妥昔单抗的 147 例患者中,移植后 EBV 再激活和 EBV PTLD 的累积发生率分别为 13%和 8%。在接受移植前利妥昔单抗的 51 例患者中,发生率分别为 2%( = .0017)和 0%( = .04)。造血恢复时间、CMV 再激活、侵袭性血流感染或确诊或疑似侵袭性真菌感染的发生率无差异。移植前给予利妥昔单抗是一种有效且无毒的干预措施,可显著降低高危患者的 EBV 再激活和 PTLD 发生率。