美罗华
医学
胸腺球蛋白
移植后淋巴增生性疾病
移植
免疫学
累积发病率
淋巴增殖性病變
入射(几何)
造血干细胞移植
内科学
胃肠病学
淋巴瘤
肾移植
光学
物理
作者
Koen van Besien,Lizamarie Bachier‐Rodriguez,Michael J. Satlin,Maxwell Brown,Usama Gergis,Danielle Guarneri,Jingmei Hsu,Adrienne A. Phillips,Sebastian Mayer,Amrita Singh,Rosemary Soave,Adriana Rossi,Catherine B. Small,Thomas J. Walsh,Hanna Rennert,Tsiporah B. Shore
标识
DOI:10.1080/10428194.2018.1543877
摘要
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/m2 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% (p = .0017) and 0% (p = .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.
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