{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,3,9]],"date-time":"2026-03-09T12:19:08Z","timestamp":1773058748007,"version":"3.50.1"},"reference-count":17,"publisher":"Wiley","issue":"6","license":[{"start":{"date-parts":[[2018,9,3]],"date-time":"2018-09-03T00:00:00Z","timestamp":1535932800000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100000054","name":"National Cancer Institute","doi-asserted-by":"publisher","award":["P30 CA008748"],"award-info":[{"award-number":["P30 CA008748"]}],"id":[{"id":"10.13039\/100000054","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Transplant Infectious Dis"],"published-print":{"date-parts":[[2018,12]]},"abstract":"<jats:title>Abstract<\/jats:title><jats:sec><jats:label\/><jats:p>Allogeneic hematopoietic cell transplant (<jats:styled-content style=\"fixed-case\">HCT<\/jats:styled-content>) recipients are at risk for herpes simplex virus (<jats:styled-content style=\"fixed-case\">HSV<\/jats:styled-content>) and varicella\u2010zoster virus (<jats:styled-content style=\"fixed-case\">VZV<\/jats:styled-content>) infections. Routine prophylaxis with acyclovir is recommended during periods of immunosuppression. Brincidofovir (<jats:styled-content style=\"fixed-case\">BCV<\/jats:styled-content>,<jats:styled-content style=\"fixed-case\"> CMX<\/jats:styled-content>001), a lipid conjugate of cidofovir, has shown in vitro activity against <jats:styled-content style=\"fixed-case\">HSV<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VZV<\/jats:styled-content>, but has not been formally studied for <jats:styled-content style=\"fixed-case\">HSV<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VZV<\/jats:styled-content> prophylaxis. We report our clinical experience of <jats:styled-content style=\"fixed-case\">BCV<\/jats:styled-content> for <jats:styled-content style=\"fixed-case\">HSV<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VZV<\/jats:styled-content> prophylaxis in <jats:styled-content style=\"fixed-case\">HCT<\/jats:styled-content> recipients. This was a retrospective review of 30 hematopoietic cell transplant (<jats:styled-content style=\"fixed-case\">HCT<\/jats:styled-content>) recipients between 8\/2010 and 8\/2015 who received <jats:styled-content style=\"fixed-case\">BCV<\/jats:styled-content> doses not exceeding 200\u00a0mg\/week for adults\/adolescents and 4\u00a0mg\/kg\/week for pediatric (&lt;12\u00a0years) patients, for \u226514\u00a0days <jats:styled-content style=\"fixed-case\">BCV<\/jats:styled-content> without concomitant acyclovir under clinical trials or single patient use. <jats:styled-content style=\"fixed-case\">HSV<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VZV<\/jats:styled-content> cases during <jats:styled-content style=\"fixed-case\">BCV<\/jats:styled-content> treatment were confirmed by viral culture or <jats:styled-content style=\"fixed-case\">PCR<\/jats:styled-content> and clinical symptoms. Of 30 patients who met the inclusion criteria, 27 (90%) patients were adults and 22 (73%) patients received T\u2010cell depleted <jats:styled-content style=\"fixed-case\">HCT<\/jats:styled-content>. The most common indications for <jats:styled-content style=\"fixed-case\">BCV<\/jats:styled-content> were cytomegalovirus in 12 patients (40%) and adenovirus in 11 patients (37%). One patient was treated for acyclovir\u2010resistant <jats:styled-content style=\"fixed-case\">HSV<\/jats:styled-content> and one for disseminated <jats:styled-content style=\"fixed-case\">VZV<\/jats:styled-content>. There were two breakthrough cases of <jats:styled-content style=\"fixed-case\">HSV<\/jats:styled-content> infection during 2170 patient\u2010days. There were no cases of breakthrough <jats:styled-content style=\"fixed-case\">VZV<\/jats:styled-content> infection. The overall rate of breakthrough <jats:styled-content style=\"fixed-case\">HSV<\/jats:styled-content> infection was 1.0 per 1000 patient\u2010days, without any breakthrough <jats:styled-content style=\"fixed-case\">VZV<\/jats:styled-content> infections. Our study provides the only available\u2014albeit limited\u2014evidence on the potential efficacy of <jats:styled-content style=\"fixed-case\">BCV<\/jats:styled-content> for <jats:styled-content style=\"fixed-case\">HSV<\/jats:styled-content>\/<jats:styled-content style=\"fixed-case\">VZV<\/jats:styled-content> prophylaxis in <jats:styled-content style=\"fixed-case\">HCT<\/jats:styled-content> patients. Additional studies are needed to further assess the efficacy and safety of <jats:styled-content style=\"fixed-case\">BCV<\/jats:styled-content> in the setting.<\/jats:p><\/jats:sec>","DOI":"10.1111\/tid.12977","type":"journal-article","created":{"date-parts":[[2018,8,18]],"date-time":"2018-08-18T11:38:31Z","timestamp":1534592311000},"update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":28,"title":["Efficacy of brincidofovir as prophylaxis against <scp>HSV<\/scp> and <scp>VZV<\/scp> in hematopoietic cell transplant recipients"],"prefix":"10.1111","volume":"20","author":[{"ORCID":"https:\/\/orcid.org\/0000-0002-2997-0217","authenticated-orcid":false,"given":"Yeon Joo","family":"Lee","sequence":"first","affiliation":[{"name":"Infectious Diseases Service Department of Medicine Memorial Sloan Kettering Cancer Center  New York New York"},{"name":"Weill Cornell Medical College Cornell University  New York New 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