Evidence map›Paper›PMID 41614327›Full record

ArticleHaemophilia : the official journal of the World Federation of Hemophilia

Lifetime Cost-Utility Analysis of Emicizumab Prophylaxis in Severe Haemophilia A Without Inhibitors in China: A Markov Model Analysis.

Han Bao, Christian Bührer, Ziyi Lin, Li Zhou, Yan Xia, Xiuze Jin, Jianwei Xuan

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Article in Haemophilia : the official journal of the World Federation of Hemophilia. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Han BaoSun Yat-Sen University, Guangzhou, China.
Christian BührerF. Hoffmann La Roche Ltd, Basel, Switzerland.
Ziyi LinLondon School of Hygiene and Tropical Medicine, London, UK.
Li ZhouThe Second Affiliated Hospital of Anhui Medical University, Hefei, China.
Yan XiaShanghai Roche Pharmaceuticals Ltd, Shanghai, China.
Xiuze JinShanghai Roche Pharmaceuticals Ltd, Shanghai, China.
Jianwei XuanSun Yat-Sen University, Guangzhou, China.

Funding

Shanghai Roche Pharmaceuticals Ltd.
6 · The paper itself

Abstract

aimAs emicizumab shares no sequence homology with factor VIII (FVIII), in patients with haemophilia A, haemostasis can be restored irrespective of the presence of FVIII inhibitors. Emicizumab, therefore, substantially improved previously available prophylactic options. This study aims to evaluate the cost-effectiveness of using emicizumab prophylaxis therapy compared to recombinant FVIII (rFVIII) prophylaxis for the treatment of severe haemophilia A.

methodsA Markov model from a Chinese healthcare system perspective using annual cycles was constructed to evaluate the lifelong costs and effectiveness. All patients started at age zero in a non-inhibitor state, treated with either emicizumab or rFVIII prophylaxis. On-demand rFVIII was given upon breakthrough bleeding for both groups. A part of severe patients developed FVIII inhibitors resulting from on-demand treatment. For patients with inhibitors, those previously treated with rFVIII prophylaxis switched to a recombinant activated factor VII (rFVIIa) on-demand only therapy, whereas those previously on emicizumab kept the same prophylactic regimen with rFVIIa for breakthrough bleeds. One immune tolerance induction (ITI) was allowed to eradicate inhibitors. Model inputs, including utility values, bleeding rates, adverse event rates and the success rate of ITI were from HAVEN 1 and 3 trials and the other literature.

resultsThe results of both the 0-12 age group and lifetime simulations demonstrated a dominant economic advantage of emicizumab prophylaxis over rFVIII prophylaxis therapy.

conclusionSevere haemophilia A patients treated by emicizumab prophylaxis can benefit both patients' QoL and economic outcomes compared to those treated by rFVIII prophylaxis.

Indexed as

Antibodies, BispecificAntibodies, Monoclonal, HumanizedCost-Benefit AnalysisCost-Effectiveness AnalysisHemophilia AChinaFactor VIIIHumansMaleMarkov ChainsRecombinant ProteinsAntibodies, BispecificAntibodies, Monoclonal, HumanizedemicizumabFactor VIIIRecombinant Proteinscost‐effectivenessemicizumab prophylaxisfactor VIII inhibitorshaemophilia Aimmune tolerance induction

Identifiers

PMID41614327
PMCPMC12984469

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.