본문으로 건너뛰기
← 뒤로

The Health Inequality Impact of Darolutamide for Nonmetastatic Castration-Resistant Prostate Cancer in the United States: A Distributional Cost-Effectiveness Analysis.

Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research 2025 Vol.28(6) p. 866-874

Jansen JP, Brewer I, Flottemesch T, Grossman JP

📝 환자 설명용 한 줄

[OBJECTIVES] Non-Hispanic (NH) Black patients are disproportionally affected by nonmetastatic castration-resistant prostate cancer (nmCRPC).

이 논문을 인용하기

BibTeX ↓ RIS ↓
APA Jansen JP, Brewer I, et al. (2025). The Health Inequality Impact of Darolutamide for Nonmetastatic Castration-Resistant Prostate Cancer in the United States: A Distributional Cost-Effectiveness Analysis.. Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research, 28(6), 866-874. https://doi.org/10.1016/j.jval.2025.03.007
MLA Jansen JP, et al.. "The Health Inequality Impact of Darolutamide for Nonmetastatic Castration-Resistant Prostate Cancer in the United States: A Distributional Cost-Effectiveness Analysis.." Value in health : the journal of the International Society for Pharmacoeconomics and Outcomes Research, vol. 28, no. 6, 2025, pp. 866-874.
PMID 40204257

Abstract

[OBJECTIVES] Non-Hispanic (NH) Black patients are disproportionally affected by nonmetastatic castration-resistant prostate cancer (nmCRPC). The objective was to quantify the health inequality impact of darolutamide + androgen deprivation therapy (ADT) relative to ADT for nmCRPC in the United States using a distributional cost-effectiveness analysis.

[METHODS] With a health economic model, quality-adjusted life years (QALYs) and costs were estimated for NH-White, NH-Black, NH-Asian, and Hispanic patients. Given the lifetime risk of nmCRPC and assuming equally distributed opportunity costs, the incremental net health benefits of darolutamide were calculated, which were used to estimate general population quality-adjusted life expectancy at birth (QALE) by race and ethnicity with and without darolutamide. The extent of QALYs and QALE differences between race and ethnicity subgroups with each strategy was quantified with an inequality index, and their difference defined as the inequality impact of darolutamide.

[RESULTS] Darolutamide + ADT resulted in an additional 1.04 (95% uncertainty interval 0.56-1.51) QALYs per treated patient relative to ADT, with the greatest gain observed among NH-Black patients (1.48 [0.48-2.71]). The relative inequality in QALYs among patients reduced by 66%, from an inequality score of 0.033 (0.004-0.082) with ADT to 0.011 (0.000-0.051) with darolutamide + ADT. Factoring in disease risk and health opportunity costs, nmCRPC treatment with darolutamide resulted in the largest net gain in QALYs among the NH-Black population, thereby having a favorable impact on inequalities in QALE.

[CONCLUSIONS] Darolutamide + ADT results in greater and a more even distribution of QALYs than ADT for nmCRPC. The greatest gains among NH-Black individuals implies a favorable health inequality impact with darolutamide.

MeSH Terms

Humans; Male; Cost-Benefit Analysis; United States; Quality-Adjusted Life Years; Prostatic Neoplasms, Castration-Resistant; Pyrazoles; Androgen Antagonists; Aged; Black or African American; Models, Economic; Healthcare Disparities; Middle Aged; Health Status Disparities; Cost-Effectiveness Analysis; White

같은 제1저자의 인용 많은 논문 (2)