Extended-duration letermovir prophylaxis for cytomegalovirus infection after cord blood transplantation in adults

Author:

Politikos Ioannis12,Lau Carmen3,Devlin Sean M.4,Quach Sean1,Lin Andrew3ORCID,Perales Miguel-Angel12ORCID,Shah Gunjan L.12,Seo Susan K.25,Papanicolaou Genovefa A.25,Barker Juliet N.12

Affiliation:

1. 1Adult Bone Marrow Transplant Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

2. 2Department of Medicine, Weill Cornell Medical College, New York, NY

3. 3Department of Pharmacy, Memorial Sloan Kettering Cancer Center, New York, NY

4. 4Department of Epidemiology and Biostatistics, Memorial Sloan Kettering Cancer Center, New York, NY

5. 5Infectious Disease Service, Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY

Abstract

Abstract Cord blood transplantation (CBT) can be complicated by a high incidence of clinically significant cytomegalovirus infection (csCMVi). We have investigated the efficacy of extended letermovir prophylaxis in seropositive adult CBT recipients. The aim was to continue prophylaxis for ≥6 months (insurance permitting). By day 100, the incidence of csCMVi was 0% in 28 patients who received letermovir prophylaxis. Moreover, of 24 patients alive at day 100, none had csCMVi by day 180, having continued prophylaxis for all (n = 20) or part (n = 4) of that period. Overall, 20 patients stopped letermovir at a median of 354 days (range, 119-455 days) posttransplant, with only 5 requiring 1 (n = 4) or 2 (n = 1) courses of valganciclovir (median total duration, 58 days; range, 12-67 days) for postprophylaxis viremia, with no subsequent csCMVi. There were no toxicities attributable to letermovir. Of the 62 historic control subjects who received acyclovir only, 51 developed csCMVi (median onset, 34 days; range, 5-74 days), for a day 100 incidence of 82% (95% confidence interval, 73-92). Seven patients developed proven/probable CMV disease, and 6 died before day 100 (3 with proven/probable CMV pneumonia). Forty-five patients required extended therapy during the first 6 months for 1 (n = 10), 2 (n = 14), or 3/persistent (n = 21) csCMVi, with 43 (84%) of 51 developing significant treatment toxicities. Letermovir is a highly effective, well-tolerated prophylaxis that mitigates CMV infection, CMV-related mortality, and antiviral therapy toxicities in CBT recipients. Our data support prophylaxis duration of at least 6 months after CBT.

Publisher

American Society of Hematology

Subject

Hematology

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