TY - JOUR
T1 - Association between antiviral prophylaxis and cytomegalovirus and epstein–barr virus dnaemia in pediatric recipients of allogeneic hematopoietic stem cell transplant
AU - Diop, Ndeye Soukeyna
AU - Enok Bonong, Pascal Roland
AU - Buteau, Chantal
AU - Duval, Michel
AU - Lacroix, Jacques
AU - Laporte, Louise
AU - Tucci, Marisa
AU - Robitaille, Nancy
AU - Spinella, Philip C.
AU - Cuvelier, Geoffrey
AU - Vercauteren, Suzanne M.
AU - Lewis, Victor
AU - Alfieri, Caroline
AU - Trottier, Helen
N1 - Funding Information:
Funding: TREASuRE study was supported by a grant from Canadian Blood Services (CBS). HT holds a salary award (Research Scholar) from the Fonds de la recherche du Québec en santé (FRQ-S) and a new Investigator Salary Award from the Canadian Institutes of Health Research (CIHR). PREB received a doctoral end-of-studies grant from the Faculty of Graduate Studies, Université de Montréal.
Funding Information:
TREASuRE study was supported by a grant from Canadian Blood Services (CBS). HT holds a salary award (Research Scholar) from the Fonds de la recherche du Qu?bec en sant? (FRQ-S) and a new Investigator Salary Award from the Canadian Institutes of Health Research (CIHR). PREB received a doctoral end-of-studies grant from the Faculty of Graduate Studies, Universit? de Montr?al.
Publisher Copyright:
© 2021 by the authors. Licensee MDPI, Basel, Switzerland.
PY - 2021/6
Y1 - 2021/6
N2 - Background: Epstein–Barr virus (EBV) and cytomegalovirus (CMV) infections can have serious consequences during the period of aplasia and lymphopenia following hematopoietic stem cell transplantation (HSCT). Large pediatric cohort studies examining the effect of antiviral prophylaxis against these viruses are scarce. The present study aimed to analyse the potential effect of antiviral prophylaxis (acyclovir and famciclovir) on active post-transplant EBV and CMV infection in a pediatric cohort of allogeneic HSCT recipients. Methods: We used data from the TREASuRE cohort, consisting of 156 patients who had a first allogeneic HSCT, enrolled in four pediatric centers in Canada between July 2013 and March 2017. Follow-up was performed from the time of transplant up to 100 days post-transplant. Adjusted hazard ratio (HR) with 95% confidence intervals (CI) for the association between antiviral prophylaxis with acyclovir and/or famciclovir and EBV and CMV DNAemia was estimated using multivariate Cox regression models. Results: The post-transplant cumulative incidence of EBV and CMV DNAemia at 100 days of follow-up were, respectively, 34.5% (95% CI: 27.6–42.6) and 19.9% (95% CI: 14.5–27.1). For acyclovir, the adjusted hazard ratio (HR) for CMV and EBV DNAemia was 0.55 (95% CI: 0.24–1.26) and 1.41 (95% CI: 0.63–3.14), respectively. For famciclovir, the adjusted HR were 0.82 (95% CI: 0.30–2.29) and 0.79 (95% CI: 0.36–1.72) for CMV and EBV DNAemia, respectively. Conclusion: The antivirals famciclovir and acyclovir did not reduce the risk of post-transplant CMV and EBV DNAemia among HSCT recipients in our pediatric population.
AB - Background: Epstein–Barr virus (EBV) and cytomegalovirus (CMV) infections can have serious consequences during the period of aplasia and lymphopenia following hematopoietic stem cell transplantation (HSCT). Large pediatric cohort studies examining the effect of antiviral prophylaxis against these viruses are scarce. The present study aimed to analyse the potential effect of antiviral prophylaxis (acyclovir and famciclovir) on active post-transplant EBV and CMV infection in a pediatric cohort of allogeneic HSCT recipients. Methods: We used data from the TREASuRE cohort, consisting of 156 patients who had a first allogeneic HSCT, enrolled in four pediatric centers in Canada between July 2013 and March 2017. Follow-up was performed from the time of transplant up to 100 days post-transplant. Adjusted hazard ratio (HR) with 95% confidence intervals (CI) for the association between antiviral prophylaxis with acyclovir and/or famciclovir and EBV and CMV DNAemia was estimated using multivariate Cox regression models. Results: The post-transplant cumulative incidence of EBV and CMV DNAemia at 100 days of follow-up were, respectively, 34.5% (95% CI: 27.6–42.6) and 19.9% (95% CI: 14.5–27.1). For acyclovir, the adjusted hazard ratio (HR) for CMV and EBV DNAemia was 0.55 (95% CI: 0.24–1.26) and 1.41 (95% CI: 0.63–3.14), respectively. For famciclovir, the adjusted HR were 0.82 (95% CI: 0.30–2.29) and 0.79 (95% CI: 0.36–1.72) for CMV and EBV DNAemia, respectively. Conclusion: The antivirals famciclovir and acyclovir did not reduce the risk of post-transplant CMV and EBV DNAemia among HSCT recipients in our pediatric population.
KW - Antiviral prophylaxis
KW - Cytomegalovirus
KW - Epstein–Barr virus
KW - Hematopoietic stem cell transplantation
KW - Human herpesvirus
KW - Pediatric
UR - http://www.scopus.com/inward/record.url?scp=85108206909&partnerID=8YFLogxK
U2 - 10.3390/vaccines9060610
DO - 10.3390/vaccines9060610
M3 - Article
C2 - 34200239
AN - SCOPUS:85108206909
SN - 2076-393X
VL - 9
JO - Vaccines
JF - Vaccines
IS - 6
M1 - 610
ER -