Literature DB >> 27696681

Dynamics of Epstein-Barr viral load after hematopoietic stem cell transplantation and effect of preemptive rituximab therapy.

Mihaja Raberahona1,2,3, Chloe Wackenheim1,2, Raphaele Germi2,4,5, Martin Carré6, Claude-Eric Bulabois6, Anne Thiébaut6,7, Julien Lupo2,4,5, Touyana Semenova2,4, Jean-Yves Cahn6, Patrice Morand2,4,5, Olivier Epaulard1,2,5.   

Abstract

BACKGROUND: Epstein-Barr virus (EBV) displays oncogenic properties, particularly in the immunocompromised host. Notably, hematopoietic stem cell transplantation (HSCT) recipients with a detectable blood EBV viral load (BEBVL) are considered at higher risk of post-transplant lymphoproliferative diseases (PTLD). Therefore, BEBVL is monitored after HSCT, and preemptive rituximab may be used in patients with high values. However, little is known about post-HSCT BEBVL dynamics, and the threshold that should lead to anti-CD20 therapy is poorly defined.
METHODS: We retrospectively analyzed the post-HSCT BEBVL of 332 adult HSCT recipients in our center from 2005 to 2013, including the effect of rituximab.
RESULTS: Detection of BEBVL >100, 1000, 5000, 10 000, and 50 000 copies/mL occurred in, respectively, 77.7%, 69.6%, 37.0%, 27.1%, and 7.5% of the patients after a respective median time of 9, 14, 15, 16, and 14 weeks. No BEBVL threshold was associated with an overall survival difference. Seventy-eight patients received rituximab, with a BEBVL decrease in most. Among patients with detectable BEBVL, long-term survival did not differ in rituximab treated and non-treated, except for patients with BEBVL ≥50 000. Only one case of PTLD was observed.
CONCLUSIONS: BEBVL is frequently detectable after HSCT, but suggests no strong association with survival. Preemptive rituximab therapy threshold remains to be defined.
© 2016 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

Entities:  

Keywords:  Epstein-Barr virus; hematopoietic stem cell transplantation; preemptive therapy; rituximab; viral load

Mesh:

Substances:

Year:  2016        PMID: 27696681     DOI: 10.1111/tid.12618

Source DB:  PubMed          Journal:  Transpl Infect Dis        ISSN: 1398-2273            Impact factor:   2.228


  6 in total

Review 1.  Post-transplantation lymphoproliferative disorder after haematopoietic stem cell transplantation.

Authors:  Francesco Pegoraro; Claudio Favre
Journal:  Ann Hematol       Date:  2021-02-06       Impact factor: 3.673

Review 2.  Epstein-Barr virus posttransplant lymphoproliferative disorder: update on management and outcomes.

Authors:  Julian Lindsay; Jad Othman; Madeleine R Heldman; Monica A Slavin
Journal:  Curr Opin Infect Dis       Date:  2021-12-01       Impact factor: 4.915

3.  Immune reconstitution of HLA-A*0201/BMLF1- and HLA-A*1101/LMP2-specific Epstein Barr virus cytotoxic T lymphocytes within 90 days after haploidentical hematopoietic stem cell transplantation.

Authors:  Ling Zhou; Dao-Pei Lu
Journal:  Virol J       Date:  2019-02-08       Impact factor: 4.099

Review 4.  Epstein-Barr Virus-Associated Post-Transplant Lymphoproliferative Disorders after Hematopoietic Stem Cell Transplantation: Pathogenesis, Risk Factors and Clinical Outcomes.

Authors:  Ayumi Fujimoto; Ritsuro Suzuki
Journal:  Cancers (Basel)       Date:  2020-02-01       Impact factor: 6.639

5.  Automated quantification of Epstein-Barr virus in whole blood for post-transplant lymphoproliferative disorders monitoring.

Authors:  Maud Salmona; Karl Stefic; Nadia Mahjoub; Flore Sicre de Fontbrune; Sarah Maylin; François Simon; Catherine Scieux; Gérard Socié; Marie-Christine Mazeron; Jérôme LeGoff
Journal:  Virol J       Date:  2020-02-03       Impact factor: 4.099

6.  The impact of Rituximab administered before transplantation in patients undergoing allogeneic hematopoietic stem cell transplantation: A real-world study.

Authors:  Xiya Wei; Yiyu Xie; Ruoyu Jiang; Huiyu Li; Heqing Wu; Yuqi Zhang; Ling Li; Shiyuan Zhou; Xiao Ma; Zaixiang Tang; Jun He; Depei Wu; Xiaojin Wu
Journal:  Front Immunol       Date:  2022-08-31       Impact factor: 8.786

  6 in total

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