A Systematic Review of Cost-Effectiveness Analyses of Novel Agents in the Treatment of Multiple Myeloma

Background: Novel therapies for multiple myeloma (MM) promise to improve outcomes but are also associated with substantial increasing costs. Evidence regarding cost-effectiveness of novel treatments is necessary, but a comprehensive up-to-date overview of the cost-effectiveness evidence of novel tre...

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Autores principales: Maarten R. Seefat, David G. J. Cucchi, Stijn Dirven, Kaz Groen, Sonja Zweegman, Hedwig M. Blommestein
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Publicado: MDPI AG 2021
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spelling oai:doaj.org-article:3e3da36cf816463da7d0e086f3846c0e2021-11-25T17:01:25ZA Systematic Review of Cost-Effectiveness Analyses of Novel Agents in the Treatment of Multiple Myeloma10.3390/cancers132256062072-6694https://doaj.org/article/3e3da36cf816463da7d0e086f3846c0e2021-11-01T00:00:00Zhttps://www.mdpi.com/2072-6694/13/22/5606https://doaj.org/toc/2072-6694Background: Novel therapies for multiple myeloma (MM) promise to improve outcomes but are also associated with substantial increasing costs. Evidence regarding cost-effectiveness of novel treatments is necessary, but a comprehensive up-to-date overview of the cost-effectiveness evidence of novel treatments is currently lacking. Methods: We searched Embase, Medline via Ovid, Web of Science and EconLIT ProQuest to identify all cost-effectiveness evaluations of novel pharmacological treatment of MM reporting cost per quality-adjusted life year (QALY) and cost per life year (LY) gained since 2005. Quality and completeness of reporting was assessed using the Consolidated Health Economic Evaluation Reporting Standards. Results: We identified 13 economic evaluations, comprising 32 comparisons. Our results show that novel agents generate additional LYs (range: 0.311–3.85) and QALYs (range: 0.1–2.85) compared to backbone regimens and 0.02 to 1.10 LYs and 0.01 to 0.91 QALYs for comparisons between regimens containing two novel agents. Lifetime healthcare costs ranged from USD 60,413 to 1,434,937 per patient. The cost-effectiveness ratios per QALY gained ranged from dominating to USD 1,369,062 for novel agents compared with backbone therapies and from dominating to USD 618,018 for comparisons between novel agents. Conclusions: Cost-effectiveness ratios of novel agents were generally above current willingness-to-pay thresholds. To ensure access, cost-effectiveness should be improved or cost-effectiveness ratios above current thresholds should be accepted.Maarten R. SeefatDavid G. J. CucchiStijn DirvenKaz GroenSonja ZweegmanHedwig M. BlommesteinMDPI AGarticlecost-effectivenessmultiple myelomaeconomic evaluationdaratumumabcarfilzomibpomalidomideNeoplasms. Tumors. Oncology. Including cancer and carcinogensRC254-282ENCancers, Vol 13, Iss 5606, p 5606 (2021)
institution DOAJ
collection DOAJ
language EN
topic cost-effectiveness
multiple myeloma
economic evaluation
daratumumab
carfilzomib
pomalidomide
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
spellingShingle cost-effectiveness
multiple myeloma
economic evaluation
daratumumab
carfilzomib
pomalidomide
Neoplasms. Tumors. Oncology. Including cancer and carcinogens
RC254-282
Maarten R. Seefat
David G. J. Cucchi
Stijn Dirven
Kaz Groen
Sonja Zweegman
Hedwig M. Blommestein
A Systematic Review of Cost-Effectiveness Analyses of Novel Agents in the Treatment of Multiple Myeloma
description Background: Novel therapies for multiple myeloma (MM) promise to improve outcomes but are also associated with substantial increasing costs. Evidence regarding cost-effectiveness of novel treatments is necessary, but a comprehensive up-to-date overview of the cost-effectiveness evidence of novel treatments is currently lacking. Methods: We searched Embase, Medline via Ovid, Web of Science and EconLIT ProQuest to identify all cost-effectiveness evaluations of novel pharmacological treatment of MM reporting cost per quality-adjusted life year (QALY) and cost per life year (LY) gained since 2005. Quality and completeness of reporting was assessed using the Consolidated Health Economic Evaluation Reporting Standards. Results: We identified 13 economic evaluations, comprising 32 comparisons. Our results show that novel agents generate additional LYs (range: 0.311–3.85) and QALYs (range: 0.1–2.85) compared to backbone regimens and 0.02 to 1.10 LYs and 0.01 to 0.91 QALYs for comparisons between regimens containing two novel agents. Lifetime healthcare costs ranged from USD 60,413 to 1,434,937 per patient. The cost-effectiveness ratios per QALY gained ranged from dominating to USD 1,369,062 for novel agents compared with backbone therapies and from dominating to USD 618,018 for comparisons between novel agents. Conclusions: Cost-effectiveness ratios of novel agents were generally above current willingness-to-pay thresholds. To ensure access, cost-effectiveness should be improved or cost-effectiveness ratios above current thresholds should be accepted.
format article
author Maarten R. Seefat
David G. J. Cucchi
Stijn Dirven
Kaz Groen
Sonja Zweegman
Hedwig M. Blommestein
author_facet Maarten R. Seefat
David G. J. Cucchi
Stijn Dirven
Kaz Groen
Sonja Zweegman
Hedwig M. Blommestein
author_sort Maarten R. Seefat
title A Systematic Review of Cost-Effectiveness Analyses of Novel Agents in the Treatment of Multiple Myeloma
title_short A Systematic Review of Cost-Effectiveness Analyses of Novel Agents in the Treatment of Multiple Myeloma
title_full A Systematic Review of Cost-Effectiveness Analyses of Novel Agents in the Treatment of Multiple Myeloma
title_fullStr A Systematic Review of Cost-Effectiveness Analyses of Novel Agents in the Treatment of Multiple Myeloma
title_full_unstemmed A Systematic Review of Cost-Effectiveness Analyses of Novel Agents in the Treatment of Multiple Myeloma
title_sort systematic review of cost-effectiveness analyses of novel agents in the treatment of multiple myeloma
publisher MDPI AG
publishDate 2021
url https://doaj.org/article/3e3da36cf816463da7d0e086f3846c0e
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