Economic Evaluation of Three BRAF + MEK Inhibitors for the Treatment of Advanced Unresectable Melanoma With BRAF Mutation From a US Payer Perspective

Author:

Halloush Shiraz1ORCID,Alkhatib Nimer S.234,Almutairi Abdulaali R.5,Calamia Mathias4,Halawah Hala4,Obeng-Kusi Mavis4,Hoyle Martin6,Rashdan Omar7ORCID,Koeller Jim89,Abraham Ivo410ORCID

Affiliation:

1. Faculty of Pharmacy, Applied Science Private University, Amman, Jordan

2. Faculty of Pharmacy, Al-Zaytoonah University of Jordan, Amman, Jordan

3. Pi Pharma Intelligence, Amman, Jordan

4. Center for Health Outcomes and PharmacoEconomic Research, The University of Arizona, Tucson, AZ, USA

5. Drug Sector, Saudi Food & Drug Authority, Riyadh, Saudi Arabia

6. Centre for the Health Economy, Macquarie University, Sydney, NSW, Australia

7. College of Pharmacy, Middle East University, Amman, Jordan

8. College of Pharmacy, University of Texas at Austin, Austin, TX, USA

9. Pharmacotherapy Education & Research Center, UT Health, San Antonio, TX, USA

10. Department of Pharmacy Practice & Science, R. Ken Coit College of Pharmacy, The University of Arizona, Tucson, AZ, USA

Abstract

Background: The combinations of BRAF + MEK inhibitors—encorafenib (ENC) + binimetinib (BIN), cobimetinib (COB) + vemurafenib (VEM), and dabrafenib (DAB) + trametinib (TRA)—are recommended for the treatment of BRAF-mutated advanced melanoma. Objective: To assess the cost-effectiveness and cost-utility of ENC + BIN versus COB + VEM versus DAB + TRA from a US payer perspective. Methods: A Markov model was constructed to simulate a hypothetical cohort over a time horizon of 10 years. The overall survival (OS) and progression-free survival (PFS) curves were independently digitized from a randomized controlled trial for ENC + BIN and fitted using R software. Published and indirectly estimated hazard ratios were used to fit OS and PFS curves for COB + VEM and DAB + TRA. Costs, life-year gains, and quality-adjusted life years (QALYs) associated with the 3 treatment combinations were estimated. A base case analysis and probabilistic sensitivity analysis (PSA) were conducted to estimate the incremental cost-utility ratio (ICUR). A discount rate of 3.5% was applied on cost and outcomes. Results: The ENC + BIN versus COB + VEM comparison was associated with an ICUR of $656 233 per QALY gained. The ENC + BIN versus DAB + TRA comparison was associated with an ICUR of $3 135 269 per QALY gained. The DAB + TRA combination dominated COB + VEM. The base case analysis estimates were confirmed by the PSA estimates. ENC + BIN was the most cost-effective combination at a high willingness-to-pay (WTP) threshold of $573 000 per QALY and $1.5 million/QALY when compared to COB + VEM and DAB + TRA, respectively. Conclusion and Relevance: Given current prices and acceptable WTP thresholds, our study suggests that DAB + TRA is the optimum treatment. In this study, ENC + BIN was cost-effective only at a very high WTP per QALY threshold.

Publisher

SAGE Publications

Subject

Pharmacology (medical)

Reference22 articles.

1. Cost-Effectiveness of Treatment Strategies for BRAF-Mutated Metastatic Melanoma

2. National Comprehensive Cancer Network. NCCN guidelines: melanoma: cutaneous. Version 3.2022. Date unknown. Accessed on December 10, 2022. https://www.nccn.org/guidelines/category_1

3. IBM. Micromedex REDBOOK. Date unknown. Accessed on September 4, 2022. https://www.ibm.com/products/micromedex-red-book

4. Systemic Therapy for Melanoma: ASCO Guideline

5. Network indirect comparison of 3 BRAF + MEK inhibitors for the treatment of advanced BRAF mutated melanoma

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