Cost–effectiveness of pembrolizumab plus chemotherapy as first-line treatment in PD-L1-positive metastatic triple-negative breast cancer

Author:

Huang Min1,Fasching Peter2,Haiderali Amin1ORCID,Pan Wilbur1,Gray Emma3,Zhou Zheng-Yi3,Hu Peter1,Chaudhuri Mitashri4,Bailly De Tilleghem Celine Le5,Cappoen Nicolas5,O’Shaughnessy Joyce6

Affiliation:

1. Merck & Co., Inc., Kenilworth, NJ, USA

2. Comprehensive Cancer Center Erlangen-EMN, University Hospital Erlangen, Department of Gynecology & Obstetrics, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany

3. Analysis Group Inc., London, UK

4. Complete HEOR Solutions (CHEORS), North Wales, PA, USA

5. MSD, HTA Statistics Europe, Brussels, Belgium

6. Baylor University Medical Center, Texas Oncology & US Oncology, Dallas, TX, USA

Abstract

Objective: This study evaluated the cost–effectiveness of pembrolizumab/chemotherapy combinations for previously untreated metastatic triple-negative breast cancer patients in the USA with PD-L1 combined positive score ≥10. Methods: A partitioned-survival model was developed to project health outcomes and direct medical costs over a 20-year time horizon. Efficacy and safety data were from randomized clinical trials. Comparative effectiveness of indirect comparators was assessed using network meta-analyses. A series of sensitivity analyses were performed to test the robustness of the results. Results: Pembrolizumab/chemotherapy resulted in total quality-adjusted life-year (QALY) gains of 0.70 years and incremental cost–effectiveness ratio of US$182,732/QALY compared with chemotherapy alone. The incremental cost–effectiveness ratio for pembrolizumab/nab-paclitaxel versus atezolizumab/nab-paclitaxel was US$44,157/QALY. Sensitivity analyses showed the results were robust over plausible values of model inputs. Conclusion: Pembrolizumab/chemotherapy is cost effective compared with chemotherapy as well as atezolizumab/nab-paclitaxel as first-line treatment for PD-L1-positive metastatic triple-negative breast cancer from a US payer perspective.

Funder

This study was funded by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.

Publisher

Future Medicine Ltd

Subject

Oncology,Immunology,Immunology and Allergy

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