Effective CMV prophylaxis with high-dose valaciclovir in allogeneic hematopoietic stem-cell recipients at a high risk of CMV infection
- Author(s)
- Douglas, G; Yong, MK; Tio, SY; Chau, M; Prabahran, A; Sasadeusz, J; Slavin, M; Ritchie, D; Chee, L;
- Details
- Publication Year 2023-02,Volume 25,Issue #1,Page e13994
- Journal Title
- Transplant Infectious Disease
- Publication Type
- Research article
- Abstract
- BACKGROUND: Cytomegalovirus (CMV) infection increases mortality and morbidity following allogeneic hematopoietic stem-cell transplantation (alloHSCT). Universal antiviral prophylaxis with letermovir is effective but unsubsidized in Australia. Valaciclovir demonstrates anti-CMV activity in high doses, but few current real-world studies explore its use as primary prophylaxis in high-risk patients post-alloHSCT. METHODS: We performed a retrospective analysis of alloHSCT recipients at high risk of clinically significant CMV infection (cs-CMVi), defined as a plasma CMV DNA viral load of >400 IU/ml requiring preemptive therapy, or CMV disease. High-risk recipients were CMV seropositive and underwent T-cell depleted, haploidentical or umbilical cord stem-cell transplants. Consecutive patients transplanted from July 2018 to January 2020, treated with valaciclovir 2 g TDS from day +7 to +100 (HD-VALA), were compared to a historical cohort (July 2017-June 2018) who only received preemptive CMV therapy, and standard valaciclovir (SD-VALA) for varicella/herpes prophylaxis. We compared incidence of and time to cs-CMVi. RESULTS: In the SD-VALA cohort (n = 27, median CMV follow-up duration 259 days), 23/27 (85%) developed cs-CMVi at a median of 39 days. For the HD-VALA cohort (n = 35, median CMV follow-up duration 216 days), 19/35 (54%) developed cs-CMVi, at a median of 68 days. Time to cs-CMVi was significantly longer in HD-VALA cohort (p < .0001). On multivariate analysis, HD VALA reduced the risk of cs-CMVi (HR 0.32, p = .0005). CONCLUSIONS: In alloHSCT recipients at high risk for cs-CMVi, HD-VALA resulted in lower cumulative reactivation, and delayed reactivation, reducing requirement for preemptive CMV therapy in the early post-engraftment period.
- Publisher
- Wiley
- Keywords
- Humans; Valacyclovir; Cytomegalovirus; Retrospective Studies; *Cytomegalovirus Infections/prevention & control; Antiviral Agents/therapeutic use; *Hematopoietic Stem Cell Transplantation/adverse effects; Cmv; bone marrow transplant; prophylaxis; valaciclovir
- Department(s)
- Clinical Haematology; Infectious Diseases
- PubMed ID
- 36413495
- Publisher's Version
- https://doi.org/10.1111/tid.13994
- Terms of Use/Rights Notice
- Refer to copyright notice on published article.
Creation Date: 2023-04-06 06:53:45
Last Modified: 2024-07-09 05:23:14