» Articles » PMID: 39797932

The Cost-Effectiveness of CDK4/6 Inhibitors in Treating HR+/HER2- Metastatic Breast Cancer Patients in the USA: When Non-medication Expenses Are Considered

Overview
Date 2025 Jan 11
PMID 39797932
Authors
Affiliations
Soon will be listed here.
Abstract

Background And Objective: Cyclin-dependent kinase (CDK)4/6 inhibitors in combination with endocrine therapy (ET) significantly enhance progression-free survival and overall survival in patients diagnosed with HR+/HER2- metastatic breast cancer (MBC). However, they are highly expensive, and their economic impact has not been fully evaluated. This is a retrospective secondary analysis evaluating the cost effectiveness of these drugs, differentiating between medication-related and non-medication costs from a healthcare perspective.

Methods: We identified 3879 patients diagnosed with MBC who received either CDK4/6i+ET (N = 2137) or ET alone (N = 1742) as first-line treatment between February 2015 and November 2021 using a USA-wide electronic health record-derived de-identified database. SEER-Medicare claims spending data were used to quantify monthly costs as a supplement to the database. Relevant costs included prescribed medications (ET and/or CDK4/6i) and overall other costs. The effectiveness was measured as progression-free duration in months. The incremental cost effectiveness ratio (ICER) analysis was conducted to examine the cost effectiveness of first-line CDK4/6i as compared with first-line ET alone.

Results: For medication costs, CDK4/6i+ET (mean cost: $240,723.7; mean effect: 19.2 months of delayed progression) compared with ET alone (mean cost: $5159.7; mean effect: 16 months without progression) resulted in an ICER of $73,098 per month of delayed progression. For non-medication costs, CDK4/6i+ET (mean cost: $43,656.6) compared with ET alone (mean cost: $66,083.5) resulted in an ICER of - $7178 per month of delayed progression.

Conclusion: The cost of treating HR+/HER2- MBC is driven by the cost of CDK4/6i. Using CDK4/6i+ET reduces non-medication costs compared to ET alone, but these savings are offset by high CDK4/6i medication costs. Lowering the market cost of CDK4/6i or targeting those who can benefit the most could improve the cost effectiveness of CDK4/6i from Medicare perspective.

References
1.
Redig A, McAllister S . Breast cancer as a systemic disease: a view of metastasis. J Intern Med. 2013; 274(2):113-26. PMC: 3711134. DOI: 10.1111/joim.12084. View

2.
Grinda T, Antoine A, Jacot W, Blaye C, Cottu P, Dieras V . Evolution of overall survival and receipt of new therapies by subtype among 20 446 metastatic breast cancer patients in the 2008-2017 ESME cohort. ESMO Open. 2021; 6(3):100114. PMC: 8095121. DOI: 10.1016/j.esmoop.2021.100114. View

3.
Welt A, Bogner S, Arendt M, Kossow J, Huffziger A, Pohlkamp C . Improved survival in metastatic breast cancer: results from a 20-year study involving 1033 women treated at a single comprehensive cancer center. J Cancer Res Clin Oncol. 2020; 146(6):1559-1566. PMC: 7230039. DOI: 10.1007/s00432-020-03184-z. View

4.
Le D, Speers C, Thompson L, Gondara L, Nichol A, Lohrisch C . The impact of new systemic therapies on survival and time on hormonal treatment in hormone receptor-positive, human epidermal growth factor receptor 2-negative metastatic breast cancer: A population-based study in British Columbia from 2003 to 2013. Cancer. 2019; 126(5):971-977. DOI: 10.1002/cncr.32631. View

5.
Gogate A, Wheeler S, Reeder-Hayes K, Ekwueme D, Fairley T, Drier S . Projecting the Prevalence and Costs of Metastatic Breast Cancer From 2015 through 2030. JNCI Cancer Spectr. 2021; 5(4). PMC: 8364673. DOI: 10.1093/jncics/pkab063. View