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Conference Paper: The cost-effectiveness of biologic/targeted synthetic/biosimilar disease modifying antirheumatic drugs: a systematic review.

TitleThe cost-effectiveness of biologic/targeted synthetic/biosimilar disease modifying antirheumatic drugs: a systematic review.
Authors
Issue Date2021
Citation
International Society for Pharmacoeconomics and Outcomes Research (ISPOR) Europe 2021 Conference: Emerging Frontiers and Opportunities: Special Populations and Technologies, Virtual Meeting, Copenhagen, Denmark, 1-3 December 2021 How to Cite?
AbstractOBJECTIVES: The clinical efficacy of biologic/targeted synthetic/biosimilar disease modifying antirheumatic drugs (b/ts/biosimilar DMARDs) in treating inflammatory arthritis is well documented, while the economic performance of these agents remains vague. This systematic review aims to identify the updated evidence of b/ts/biosimilar DMARDs cost-effectiveness in the management of inflammatory arthritis to inform prescribing and formulary listing decisions. METHODS: We conducted a systematic review on cost-effectiveness of b/ts/biosimilar DMARDs in treating inflammatory arthritis through five databases. We summarized the cost-effectiveness results comparing b/ts/biosimilar DMARDs versus conventional synthetic DMARDs (csDMARDs). We then conducted secondary analysis on extracted data to calculate the incremental cost-utility ratio (ICUR) to facilitate the comparison among different b/ts/biosimilar DMARDs. We assessed the impact of indirect costs (i.e., non-medical costs incurred due to disease) on ICUR. We also estimated the potential medical cost reduction when using biosimilars. RESULTS: We identified 58 publications covering four types of inflammatory arthritis: rheumatoid arthritis, juvenile idiopathic arthritis, ankylosing spondylitis, and psoriatic arthritis. For patients with inadequate response to csDMARDs, less than half of the comparisons concluded that b/ts/biosimilar DMARDs is cost-effective than csDMARDs, despite the former providing significant improvements on quality-adjusted life-year (QALY). More than 88% of studies reported the new generation b/tsDMARDs have lower costs and comparable QALY gain compared to the old generation. Accounting indirect costs leads to 11.9-60.4% of ICURs reduction. Introducing biosimilar DMARDs is associated with 1.7-16.7% medical costs reduction comparing to their bio-originators. CONCLUSIONS: B/ts/biosimilar DMARDs are consistently reported with profound QALY improvement and considerable reduction of indirect costs compared to csDMARDs. However, current economic evidence does not fully support the cost-effectiveness of b/ts/biosimilar DMARDs in treating patients with inflammatory arthritis. New generation b/ts/biosimilar DMARDs showed better cost-effectiveness may become favorable in the future market.
DescriptionPoster Presentation - code POSB99
Persistent Identifierhttp://hdl.handle.net/10722/306248

 

DC FieldValueLanguage
dc.contributor.authorPeng, K-
dc.contributor.authorLi, X-
dc.contributor.authorCheng, WT-
dc.contributor.authorTong, X-
dc.contributor.authorYeung, WYW-
dc.contributor.authorHo, CTK-
dc.contributor.authorLau, WCS-
dc.date.accessioned2021-10-20T10:20:54Z-
dc.date.available2021-10-20T10:20:54Z-
dc.date.issued2021-
dc.identifier.citationInternational Society for Pharmacoeconomics and Outcomes Research (ISPOR) Europe 2021 Conference: Emerging Frontiers and Opportunities: Special Populations and Technologies, Virtual Meeting, Copenhagen, Denmark, 1-3 December 2021-
dc.identifier.urihttp://hdl.handle.net/10722/306248-
dc.descriptionPoster Presentation - code POSB99-
dc.description.abstractOBJECTIVES: The clinical efficacy of biologic/targeted synthetic/biosimilar disease modifying antirheumatic drugs (b/ts/biosimilar DMARDs) in treating inflammatory arthritis is well documented, while the economic performance of these agents remains vague. This systematic review aims to identify the updated evidence of b/ts/biosimilar DMARDs cost-effectiveness in the management of inflammatory arthritis to inform prescribing and formulary listing decisions. METHODS: We conducted a systematic review on cost-effectiveness of b/ts/biosimilar DMARDs in treating inflammatory arthritis through five databases. We summarized the cost-effectiveness results comparing b/ts/biosimilar DMARDs versus conventional synthetic DMARDs (csDMARDs). We then conducted secondary analysis on extracted data to calculate the incremental cost-utility ratio (ICUR) to facilitate the comparison among different b/ts/biosimilar DMARDs. We assessed the impact of indirect costs (i.e., non-medical costs incurred due to disease) on ICUR. We also estimated the potential medical cost reduction when using biosimilars. RESULTS: We identified 58 publications covering four types of inflammatory arthritis: rheumatoid arthritis, juvenile idiopathic arthritis, ankylosing spondylitis, and psoriatic arthritis. For patients with inadequate response to csDMARDs, less than half of the comparisons concluded that b/ts/biosimilar DMARDs is cost-effective than csDMARDs, despite the former providing significant improvements on quality-adjusted life-year (QALY). More than 88% of studies reported the new generation b/tsDMARDs have lower costs and comparable QALY gain compared to the old generation. Accounting indirect costs leads to 11.9-60.4% of ICURs reduction. Introducing biosimilar DMARDs is associated with 1.7-16.7% medical costs reduction comparing to their bio-originators. CONCLUSIONS: B/ts/biosimilar DMARDs are consistently reported with profound QALY improvement and considerable reduction of indirect costs compared to csDMARDs. However, current economic evidence does not fully support the cost-effectiveness of b/ts/biosimilar DMARDs in treating patients with inflammatory arthritis. New generation b/ts/biosimilar DMARDs showed better cost-effectiveness may become favorable in the future market.-
dc.languageeng-
dc.relation.ispartofISPOR Europe Conference 2021-
dc.titleThe cost-effectiveness of biologic/targeted synthetic/biosimilar disease modifying antirheumatic drugs: a systematic review.-
dc.typeConference_Paper-
dc.identifier.emailPeng, K: kpeng420@hku.hk-
dc.identifier.emailLi, X: sxueli@hku.hk-
dc.identifier.emailTong, X: xinntong@hku.hk-
dc.identifier.emailHo, CTK: ctkho@hkucc.hku.hk-
dc.identifier.emailLau, WCS: cslau@hku.hk-
dc.identifier.authorityLi, X=rp02531-
dc.identifier.authorityLau, WCS=rp01348-
dc.identifier.hkuros328217-

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