| Literature DB >> 30741059 |
Koen Van Besien1, Lizamarie Bachier-Rodriguez1, Michael Satlin2, Maxwell A Brown3, Usama Gergis1, Danielle Guarneri1, Jingmei Hsu1, Adrienne A Phillips1, Sebastian A Mayer1, Amrita D Singh3, Rosemary Soave2, Adriana Rossi1, Catherine B Small2, Thomas J Walsh2, Hanna Rennert4, Tsiporah B Shore1.
Abstract
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.Entities:
Keywords: EBV; Epstein–Barr virus; PTLD; rituximab; transplant toxicity
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Year: 2019 PMID: 30741059 DOI: 10.1080/10428194.2018.1543877
Source DB: PubMed Journal: Leuk Lymphoma ISSN: 1026-8022