Cost-effectiveness of emicizumab for the treatment of hemophilia A: a systematic review

BackgroundEmicizumab, a bispecific factor IXa- and factor X-directed antibody indicated for routine prophylaxis of bleeding episodes in people with hemophilia A, can impose a significant financial burden. We conducted a systematic review to evaluate the reporting quality of existing pharmacoeconomic...

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Published in:Frontiers in Public Health
Main Authors: Min Chen, Yunzhu Lin, Guoqian He, Liang Huang, Junyi Han, Jiaqi Ni
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-10-01
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fpubh.2025.1658760/full
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author Min Chen
Min Chen
Min Chen
Yunzhu Lin
Yunzhu Lin
Guoqian He
Liang Huang
Liang Huang
Junyi Han
Jiaqi Ni
Jiaqi Ni
Jiaqi Ni
author_facet Min Chen
Min Chen
Min Chen
Yunzhu Lin
Yunzhu Lin
Guoqian He
Liang Huang
Liang Huang
Junyi Han
Jiaqi Ni
Jiaqi Ni
Jiaqi Ni
author_sort Min Chen
collection DOAJ
container_title Frontiers in Public Health
description BackgroundEmicizumab, a bispecific factor IXa- and factor X-directed antibody indicated for routine prophylaxis of bleeding episodes in people with hemophilia A, can impose a significant financial burden. We conducted a systematic review to evaluate the reporting quality of existing pharmacoeconomic studies on emicizumab, and to synthesize its cost-effectiveness for hemophilia A treatment.MethodsDatabases including PubMed, Embase, Cochrane Library, National Health Service Economic Evaluation Database, Health Technology Assessment, China National Knowledge Infrastructure, VIP China Science and Technology Journal database, and WanFang were searched for pharmacoeconomic studies on emicizumab. The general information, methods, and results of the retrieved studies were analyzed. The reporting quality of the studies was evaluated with the Consolidated Health Economic Evaluation Reporting Standards (CHEERS) 2022 checklist.ResultsA total of 163 studies were retrieved, and 17 studies were further analyzed. Emicizumab was compared to bypassing agents (BPAs), recombinant factor VIII (rFVIII), recombinant factor VIII Fc fusion protein (rFVIIIFc), and gene therapy. The reporting quality of the studies is generally good with an average score of 79.64% (22.3/28) based on the CHEERS 2022 checklist. Current studies revealed that emicizumab prophylaxis was more cost-effective compared to BPAs in people with hemophilia A with inhibitors. However, its cost-effectiveness compared to rFVIII was unclear and varied across different countries. In addition, rFVIIIFc and valoctocogene roxaparvovec were more cost-effective than emicizumab for people with HA without inhibitors.ConclusionEmicizumab prophylaxis was more cost-effective compared to BPAs in people with hemophilia A with inhibitors. Cost-effectiveness analyses with more accurate cost estimations of different countries should provide more convincing evidence for clinical decision-making.Systematic review registrationIdentifier CRD 42023429349, https://www.crd.york.ac.uk/PROSPERO/view/CRD42023429349.
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spelling doaj-art-e77b86d0bcc14003bba0ea2f5a5fdbc62025-10-07T05:34:15ZengFrontiers Media S.A.Frontiers in Public Health2296-25652025-10-011310.3389/fpubh.2025.16587601658760Cost-effectiveness of emicizumab for the treatment of hemophilia A: a systematic reviewMin Chen0Min Chen1Min Chen2Yunzhu Lin3Yunzhu Lin4Guoqian He5Liang Huang6Liang Huang7Junyi Han8Jiaqi Ni9Jiaqi Ni10Jiaqi Ni11Department of Pharmacy/Evidence-Based Pharmacy Center, West China Second University Hospital, Sichuan University, Chengdu, ChinaKey Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, ChinaWest China School of Pharmacy, Sichuan University, Chengdu, ChinaDepartment of Pharmacy/Evidence-Based Pharmacy Center, West China Second University Hospital, Sichuan University, Chengdu, ChinaKey Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, ChinaDepartment of Pediatric Hematology and Oncology, West China Second University Hospital, Sichuan University, Chengdu, ChinaDepartment of Pharmacy/Evidence-Based Pharmacy Center, West China Second University Hospital, Sichuan University, Chengdu, ChinaKey Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, ChinaWest China School of Pharmacy, Sichuan University, Chengdu, ChinaDepartment of Pharmacy/Evidence-Based Pharmacy Center, West China Second University Hospital, Sichuan University, Chengdu, ChinaKey Laboratory of Birth Defects and Related Diseases of Women and Children, Sichuan University, Ministry of Education, Chengdu, ChinaWest China School of Pharmacy, Sichuan University, Chengdu, ChinaBackgroundEmicizumab, a bispecific factor IXa- and factor X-directed antibody indicated for routine prophylaxis of bleeding episodes in people with hemophilia A, can impose a significant financial burden. We conducted a systematic review to evaluate the reporting quality of existing pharmacoeconomic studies on emicizumab, and to synthesize its cost-effectiveness for hemophilia A treatment.MethodsDatabases including PubMed, Embase, Cochrane Library, National Health Service Economic Evaluation Database, Health Technology Assessment, China National Knowledge Infrastructure, VIP China Science and Technology Journal database, and WanFang were searched for pharmacoeconomic studies on emicizumab. The general information, methods, and results of the retrieved studies were analyzed. The reporting quality of the studies was evaluated with the Consolidated Health Economic Evaluation Reporting Standards (CHEERS) 2022 checklist.ResultsA total of 163 studies were retrieved, and 17 studies were further analyzed. Emicizumab was compared to bypassing agents (BPAs), recombinant factor VIII (rFVIII), recombinant factor VIII Fc fusion protein (rFVIIIFc), and gene therapy. The reporting quality of the studies is generally good with an average score of 79.64% (22.3/28) based on the CHEERS 2022 checklist. Current studies revealed that emicizumab prophylaxis was more cost-effective compared to BPAs in people with hemophilia A with inhibitors. However, its cost-effectiveness compared to rFVIII was unclear and varied across different countries. In addition, rFVIIIFc and valoctocogene roxaparvovec were more cost-effective than emicizumab for people with HA without inhibitors.ConclusionEmicizumab prophylaxis was more cost-effective compared to BPAs in people with hemophilia A with inhibitors. Cost-effectiveness analyses with more accurate cost estimations of different countries should provide more convincing evidence for clinical decision-making.Systematic review registrationIdentifier CRD 42023429349, https://www.crd.york.ac.uk/PROSPERO/view/CRD42023429349.https://www.frontiersin.org/articles/10.3389/fpubh.2025.1658760/fullhemophilia Aemicizumabcost-effectivenesssystematic reviewpharmacoeconomic
spellingShingle Min Chen
Min Chen
Min Chen
Yunzhu Lin
Yunzhu Lin
Guoqian He
Liang Huang
Liang Huang
Junyi Han
Jiaqi Ni
Jiaqi Ni
Jiaqi Ni
Cost-effectiveness of emicizumab for the treatment of hemophilia A: a systematic review
hemophilia A
emicizumab
cost-effectiveness
systematic review
pharmacoeconomic
title Cost-effectiveness of emicizumab for the treatment of hemophilia A: a systematic review
title_full Cost-effectiveness of emicizumab for the treatment of hemophilia A: a systematic review
title_fullStr Cost-effectiveness of emicizumab for the treatment of hemophilia A: a systematic review
title_full_unstemmed Cost-effectiveness of emicizumab for the treatment of hemophilia A: a systematic review
title_short Cost-effectiveness of emicizumab for the treatment of hemophilia A: a systematic review
title_sort cost effectiveness of emicizumab for the treatment of hemophilia a a systematic review
topic hemophilia A
emicizumab
cost-effectiveness
systematic review
pharmacoeconomic
url https://www.frontiersin.org/articles/10.3389/fpubh.2025.1658760/full
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