Oral brincidofovir decreases the incidence of HHV-6B viremia after allogeneic HCT Journal Article


Authors: Hill, J. A.; Nichols, W. G.; Marty, F. M.; Papanicolaou, G. A.; Brundage, T. M.; Lanier, R.; Zerr, D. M.; Boeckh, M. J.
Article Title: Oral brincidofovir decreases the incidence of HHV-6B viremia after allogeneic HCT
Abstract: Human herpesvirus 6B (HHV-6B) frequently reactivates after allogeneic hematopoietic cell transplantation (HCT). There are no randomized studies of antiviral treatments to prevent HHV-6B reactivation. Brincidofovir has high in vitro activity against HHV-6B and other DNA viruses, but its in vivo activity for HHV-6B has not been demonstrated. We performed a post hoc analysis of a randomized controlled trial of twice-weekly oral brincidofovir for cytomegalovirus prophylaxis after allogeneic HCT to study the effect of brincidofovir on HHV-6B reactivation. We included patients randomized within 2 weeks of HCT and who received at least 6 consecutive doses of study drug after randomization. We tested plasma for HHV-6B through week 6 post-HCT. The cohort consisted of 92 patients receiving brincidofovir and 61 receiving placebo. The cumulative incidence of HHV-6B plasma detection through day 42 post-HCT was significantly lower among patients receiving brincidofovir (14.2%) compared with placebo (32.4%; log-rank, 0.019). In an adjusted Cox model, brincidofovir exposure remained associated with a lower hazard for HHV-6B plasma detection (hazard ratio, 0.40; 95% confidence interval, 0.20-0.80). In conclusion, brincidofovir prophylaxis reduced HHV-6B reactivation after allogeneic HCT in a post hoc analysis of a randomized controlled trial. These data support the study of intravenous brincidofovir for HHV-6B prophylaxis.
Keywords: risk; foscarnet; therapy; cell transplantation; reconstitution; reactivation; preemptive; human herpesvirus-6 encephalitis
Journal Title: Blood
Volume: 135
Issue: 17
ISSN: 0006-4971
Publisher: American Society of Hematology  
Date Published: 2020-04-23
Start Page: 1447
End Page: 1451
Language: English
ACCESSION: WOS:000534367800009
DOI: 10.1182/blood.2019004315
PROVIDER: wos
PMCID: PMC7180083
PUBMED: 32076716
Notes: Article -- Source: Wos
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