Impact of Primary Letermovir Prophylaxis Versus Preemptive Antiviral Therapy for Cytomegalovirus on Economic and Clinical Outcomes after Hematopoietic Cell Transplantation

被引:1
|
作者
Tan, Carrie A. [1 ]
Palen, Lauren [2 ,3 ]
Su, Yiqi [4 ]
Li, Yuxuan [4 ]
Gennarelli, Renee L. [5 ]
Perales, Miguel-Angel [3 ,6 ]
Cohen, Nina [2 ]
Papanicolaou, Genovefa A. [4 ,6 ]
Shah, Gunjan L. [3 ,6 ]
Seo, Susan K. [4 ,6 ]
机构
[1] City Hope Natl Med Ctr, Dept Pharm, Duarte, CA USA
[2] Mem Sloan Kettering Canc Ctr, Dept Pharm, New York, NY USA
[3] Mem Sloan Kettering Canc Ctr, Adult Bone Marrow Transplant Serv, New York, NY USA
[4] Mem Sloan Kettering Canc Ctr, Infect Dis Serv, New York, NY USA
[5] Xcenda LLC, Real World Evidence, Conshohocken, PA USA
[6] Weill Cornell Med Coll, Dept Med, New York, NY USA
来源
TRANSPLANTATION AND CELLULAR THERAPY | 2024年 / 30卷 / 08期
基金
美国国家卫生研究院;
关键词
Allogeneic hematopoi- etic cell transplantation; Cost analysis; Cytomegalovirus; Letermovir prophylaxis; Preemptive therapy; DISEASE; INFECTION; COMPLICATIONS; RECIPIENTS; DURATION; BLOOD; RISK;
D O I
10.1016/j.jtct.2024.05.021
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Preemptive therapy (PET) historically has been the primary strategy to reduce early- onset cytomegalovirus (CMV) reactivation after allogeneic hematopoietic cell transplantation (HCT) but is associated with antiviral-associated toxicities and increases in healthcare resource utilization and cost. Despite its high cost, letermovir (LTV) prophylaxis has largely supplanted PET due to its effectiveness and tolerability. Direct comparisons between LTV and PET approaches on economic and clinical outcomes after allogeneic HCT remain limited. Objective: To compare total cost of care (inpatient and outpatient) between LTV prophylaxis and PET through day+180 after allogeneic HCT. Adult allogeneic CMV seropositive (R+) HCT recipients who initiated LTV <30 days after HCT between 01/ 01/18 and 12/31/18 were matched 1:1 to allogeneic CMV R+ HCT recipients between 01/ 01/15 and 12/31/17 (PET cohort). Patients were grouped into high-risk (HR) or standard- risk (SR) for CMV to compare the LTV and PET cohorts. Direct costs for each patient's index HCT admission and all subsequent inpatient and outpatient care through day+180 after HCT were determined and converted into 2021 US dollars and then to Medicare proportional dollars (MPD). A secondary analysis using 2019 average wholesale price was conducted to specifically evaluate anti-CMV medication costs. There were a total of 176 patients with 54 HR CMV pairs and 34 SR CMV pairs. No differences in survival between LTV and PET for both HR and SR CMV groups were observed. The rate of clinically significant CMV infection decreased for both HR CMV (11/54, 20.4% versus 38/54, 70.4%, P < .001) and SR CMV (1/34, 2.9% versus 12/34, 35.3%, P < .001) patients who were given LTV prophylaxis with corresponding reductions in val(ganciclovir) and foscarnet (HR CMV only) use. Among HR CMV patients, LTV prophylaxis was associated with reduc- tions in CMV-related readmissions (3/54, 5.6% versus 18/54, 33.3%, P < .001) and outpa- tient visits within the first 100 days after HCT (20 versus 25, P = .002), and a decreased median total cost of care ($36,018 versus $75,525, P < .001) in MPD was observed. For SR CMV patients on LTV, a significant reduction in the median inpatient cost ($15,668 versus $27,818, P < .001) was found, but this finding was offset by a higher median outpatient cost ($26,145 versus $20,307, P = .030) that was not CMV-driven. LTV prophylaxis is highly effective in reducing clinically significant CMV reactivations for both HR and SR HCT recipients. In this study, LTV prophylaxis was associated with a decreased total cost of care for HR CMV patients through day+180. Specifically, reductions in CMV-related readmissions, exposure to CMV-directed antiviral agents, and outpatient visits in the first 100 days after HCT were observed. SR CMV patients receiving LTV prophylaxis benefited by having a reduced inpatient cost of care due to lowered room and pharmacy costs.
引用
收藏
页码:792e1 / 792e12
页数:12
相关论文
共 50 条
  • [31] Pharmacokinetics, Safety, and Efficacy of Letermovir for Cytomegalovirus Prophylaxis in Adolescent Hematopoietic Cell Transplantation Recipients
    Groll, Andreas H.
    Schulte, Johannes H.
    Antmen, Ali Buelent
    Fraser, Christopher J.
    Teal, Valerie L.
    Haber, Barbara
    Caro, Luzelena
    McCrea, Jacqueline B.
    Fancourt, Craig
    Patel, Mayankbhai
    Menzel, Karsten
    Badshah, Cyrus
    PEDIATRIC INFECTIOUS DISEASE JOURNAL, 2024, 43 (03) : 203 - 208
  • [32] Letermovir prophylaxis for cytomegalovirus in pediatric patients undergoing allogeneic hematopoietic stem cell transplantation
    Wang, Qingwei
    Liu, Minyuan
    Zhang, Senlin
    Gao, Li
    Chu, Xinran
    Li, Bohan
    Cheng, Shengqin
    Tian, Yuanyuan
    Zhang, Yongping
    Hu, Yixin
    Li, Jie
    Lu, Jun
    Xiao, Peifang
    Liu, Hu
    Hu, Shaoyan
    BONE MARROW TRANSPLANTATION, 2025, : 422 - 424
  • [33] Valacyclovir prophylaxis versus preemptive valganciclovir therapy to prevent cytomegalovirus disease after renal transplantation
    Reischig, T.
    Jindra, P.
    Hes, O.
    Svecova, M.
    Klaboch, J.
    Treska, V.
    AMERICAN JOURNAL OF TRANSPLANTATION, 2008, 8 (01) : 69 - 77
  • [34] Risk factor analysis for cytomegalovirus reactivation under prophylaxis with letermovir after allogeneic hematopoietic stem cell transplantation
    Mizuno, Kota
    Sakurai, Masatoshi
    Kato, Jun
    Yamaguchi, Kentaro
    Abe, Ryohei
    Koda, Yuya
    Kataoka, Keisuke
    Mori, Takehiko
    TRANSPLANT INFECTIOUS DISEASE, 2022, 24 (06)
  • [36] Letermovir Resistance Genotyping in a Clinical Trial of Cytomegalovirus Prophylaxis for Hematopoietic Cell Transplant Recipients
    Douglas, Cameron M.
    Levitan, Diane
    Maguire, Maureen
    Chen, Lei
    Wei, Bo
    Barnard, Richard
    Nickle, David
    BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2018, 24 (03) : S72 - S72
  • [37] Single center real-world data on Letermovir prophylaxis for cytomegalovirus reactivation after allogeneic hematopoietic cell transplantation
    Derigs, P.
    Schubert, M. -L.
    Schnitzler, P.
    Mueller-Tidow, C.
    Dreger, P.
    Schmitt, M.
    ONCOLOGY RESEARCH AND TREATMENT, 2019, 42 : 173 - 173
  • [38] Preemptive oral ganciclovir therapy versus prophylaxis to prevent symptomatic cytomegalovirus infection after kidney transplantation
    Jung, C
    Engelmann, E
    Borner, K
    Offermann, G
    TRANSPLANTATION PROCEEDINGS, 2001, 33 (7-8) : 3621 - 3623
  • [40] Cytomegalovirus (CMV)-Specific Polyfunctional T-Cell Responses after Letermovir (LET) Prophylaxis in Hematopoietic Cell Transplantation (HCT)
    Zamora, Danniel
    Akoto, Brenda
    Xie, Hu
    Kiener, Richard
    Edmison, Bradley C.
    Stevens-Ayers, Terry
    Wagner, Ralf
    Mielcarek, Marco
    Leisenring, Wendy M.
    De Rosa, Stephen
    Boeckh, Michael
    BIOLOGY OF BLOOD AND MARROW TRANSPLANTATION, 2020, 26 (03) : S68 - S69