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Efficacy of brincidofovir as prophylaxis against HSV and VZV in hematopoietic cell transplant recipients
Author(s) -
Lee Yeon Joo,
Neofytos Dionysios,
Kim Seong Jin,
Cheteyan Leslie,
Huang YaoTing,
Papadopoulos Esperanza B.,
Jakubowski Ann A.,
Papanicolaou Genovefa A.
Publication year - 2018
Publication title -
transplant infectious disease
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.69
H-Index - 67
eISSN - 1399-3062
pISSN - 1398-2273
DOI - 10.1111/tid.12977
Subject(s) - medicine , varicella zoster virus , herpes simplex virus , cidofovir , immunosuppression , clinical trial , concomitant , hematopoietic cell , virology , immunology , virus , haematopoiesis , stem cell , biology , genetics
Allogeneic hematopoietic cell transplant ( HCT ) recipients are at risk for herpes simplex virus ( HSV ) and varicella‐zoster virus ( VZV ) infections. Routine prophylaxis with acyclovir is recommended during periods of immunosuppression. Brincidofovir ( BCV , CMX 001), a lipid conjugate of cidofovir, has shown in vitro activity against HSV / VZV , but has not been formally studied for HSV / VZV prophylaxis. We report our clinical experience of BCV for HSV / VZV prophylaxis in HCT recipients. This was a retrospective review of 30 hematopoietic cell transplant ( HCT ) recipients between 8/2010 and 8/2015 who received BCV doses not exceeding 200 mg/week for adults/adolescents and 4 mg/kg/week for pediatric (<12 years) patients, for ≥14 days BCV without concomitant acyclovir under clinical trials or single patient use. HSV / VZV cases during BCV treatment were confirmed by viral culture or PCR and clinical symptoms. Of 30 patients who met the inclusion criteria, 27 (90%) patients were adults and 22 (73%) patients received T‐cell depleted HCT . The most common indications for BCV were cytomegalovirus in 12 patients (40%) and adenovirus in 11 patients (37%). One patient was treated for acyclovir‐resistant HSV and one for disseminated VZV . There were two breakthrough cases of HSV infection during 2170 patient‐days. There were no cases of breakthrough VZV infection. The overall rate of breakthrough HSV infection was 1.0 per 1000 patient‐days, without any breakthrough VZV infections. Our study provides the only available—albeit limited—evidence on the potential efficacy of BCV for HSV / VZV prophylaxis in HCT patients. Additional studies are needed to further assess the efficacy and safety of BCV in the setting.