Abstract 1780P
Background
In the backdrop of keener scrutiny of health equity issues, the impact of a new intervention on inequality in health outcomes is increasingly viewed as an element in health technology assessment. Non-Hispanic (NH) Black patients are disproportionally affected by non-metastatic castration-resistant prostate cancer (nmCRPC). Darolutamide is an approved treatment for nmCRPC and was shown to be effective and safe among NH-Black patients in the ARAMIS trial. The objective of this study was to quantify the health inequality impact of darolutamide+ androgen-deprivation therapy (ADT) relative to ADT for nmCRPC in the U.S. by means of a distributional cost-effectiveness analysis.
Methods
With a decision model, the quality-adjusted life years (QALYs) and costs were estimated for NH-White, NH-Black, Asian, and Hispanic patients. The degree of differences in QALYs among these subgroups was expressed with Atkinson relative inequality indices (0 = equal outcomes and 1 = maximum inequality between subgroups) for both strategies. Their difference was defined as the inequality impact of darolutamide among treated patients. Subtracting equally distributed health opportunity costs from the QALY gains with darolutamide facilitated calculation of the overall health inequality impact across population subgroups.
Results
Darolutamide+ADT resulted in an additional 1.04 (95% confidence interval 0.57; 1.49) QALYs per treated patient relative to ADT, with the greatest gain observed among NH-Black patients (1.48 QALYs (0.49; 2.72)). The relative inequality in QALYs among patients reduced by 66%, from an inequality score of 0.032 (0.004; 0.080) with ADT to 0.011 (0.000; 0.049) with darolutamide+ADT. Factoring in health opportunity costs, treatment of eligible nmCRPC patients with darolutamide resulted in the largest net gain in QALYs among the NH-Black population, thereby having a favorable impact on inequalities in quality adjusted life expectancy.
Conclusions
Darolutamide+ADT for the treatment of nmCRPC results in greater health outcomes than ADT, and reduces inequality in health outcomes across subgroups according to race and ethnicity in the U.S.
Clinical trial identification
Editorial acknowledgement
Legal entity responsible for the study
The authors.
Funding
Bayer Pharmaceuticals.
Disclosure
J. Janssen, T. Flottemesch, I. Brewer, P. Sullivan: Financial Interests, Institutional, Full or part-time Employment, Precision heor was hired by Bayer to perform the research: PRECISIONheor. J. Partridge: Financial Interests, Personal, Full or part-time Employment, Full time employee of Bayer: Bayer Pharmaceuticals.
Resources from the same session
1794P - Prognostic role of metastatic site in patients with de novo metastatic prostate cancer: A population-based analysis in new hormonal agents era
Presenter: Emre Yekeduz
Session: Poster session 14
1795P - China ARCHES: A multicenter phase III randomized double-blind placebo (PBO)-controlled efficacy and safety trial of enzalutamide (ENZA) + androgen deprivation therapy (ADT) vs PBO + ADT in Chinese patients (pts) with metastatic hormone-sensitive prostate cancer (mHSPC)
Presenter: Gongqian Zeng
Session: Poster session 14
1796P - Real-world analysis of metastatic hormone-sensitive prostate cancer: Are randomized clinical trials more trustworthy? Insights from PIONEER, the European network of excellence for big data in prostate cancer
Presenter: Juan Gómez Rivas
Session: Poster session 14
1797P - Application of novel machine learning model in [68Ga] Ga-PSMA-11 PET/CT: Predicting survival in oligometastatic prostate cancer patients
Presenter: Mikaela Dell'Oro
Session: Poster session 14
1800P - Differential tumor gene-expression profiling of patients (pts) with de-novo metastatic castration-sensitive prostate cancer (dn-mCSPC) versus (vs.) mCSPC relapsing after prior localized therapy (PLT-mCSPC)
Presenter: Vinay Mathew Thomas
Session: Poster session 14
1803P - Phase I/II study of bavdegalutamide, a PROTAC androgen receptor (AR) degrader in metastatic castration-resistant prostate cancer (mCRPC): Radiographic progression-free survival (rPFS) in patients (pts) with <italic>AR</italic> ligand-binding domain (LBD) mutations
Presenter: Daniel Petrylak
Session: Poster session 14