Letermovir as Cytomegalovirus Prophylaxis in a Pediatric Cohort: A Retrospective Analysis

被引:27
作者
Kuhn, Alexis [1 ,5 ]
Puttkammer, Jenna [2 ]
Madigan, Theresa [3 ]
Dinnes, Laura [1 ]
Khan, Shakila [4 ]
Ferdjallah, Asmaa [4 ]
Kohorst, Mira [4 ]
机构
[1] Mayo Clin, Dept Pharm, Rochester, MN USA
[2] North Mem Hlth Hosp, Dept Pharm, Robbinsdale, MN USA
[3] Mayo Clin, Div Pediat Infect Dis, Rochester, MN USA
[4] Mayo Clin, Div Pediat Hematol Oncol Bone Marrow Transplant, Rochester, MN USA
[5] 200 First St SW, Rochester, MN 55905 USA
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2023年 / 29卷 / 01期
关键词
Letermovir; Children; Adolescents; Cytomegalovirus; Hematopoietic stem cell trans; plantation; STEM-CELL TRANSPLANTATION; INFECTION; GANCICLOVIR; CHILDREN; DISEASE;
D O I
10.1016/j.jtct.2022.10.005
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Letermovir is an attractive cytomegalovirus (CMV) prophylactic agent, but published data in children are scarce. This retrospective chart review aimed to describe our experience using letermovir as CMV prophylaxis in pediatric hematopoietic cell transplantation (HCT) recipients. Pediatric patients (age <20 years) undergoing allogeneic HCT and receiving letermovir prophylaxis in the Mayo Clinic Pediatric Bone Marrow Transplant Program were eligible for inclusion in this retrospective chart review. Medical records were reviewed to evaluate letermovir dosing, CMV levels, laboratory values, and reports of adverse effects. Between October 2020 and April 2022, 9 patients age 4 to 19 years undergoing allogeneic HCT in the Pediatric Bone Marrow Transplant Program received letermovir prophylaxis, either 240 mg or 480 mg daily at a mean and median dose of 10 mg/kg/day. Letermovir was crushed and administered via nasogastric tube in 4 of 9 patients. Two patients received letermovir for secondary CMV prophylaxis after initial treatment with ganciclovir/valganciclovir, and the remaining 7 received letermovir for primary prophylaxis. One patient, a 20-kg 6-year-old female receiving 240 mg (12 mg/kg), experienced lowlevel CMV viremia while on letermovir. No other patients experienced CMV reactivation while on letermovir prophylaxis. In 2 patients, transient mild transaminitis was noted within the first weeks of letermovir therapy, which resolved without intervention, and its relationship to letermovir could not be clearly established. Letermovir administration was feasible and well tolerated as CMV prophylaxis in our small cohort of pediatric patients undergoing HCT. Larger, prospective studies are warranted to confirm the safety and efficacy of letermovir in children. (c) 2022 American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. (c) 2022 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:62.e1 / 62.e4
页数:4
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