Cost-effectiveness of talazoparib plus enzalutamide as first-line therapy in metastatic castration-resistant prostate cancer

Read the full article See related articles

Listed in

This article is not in any list yet, why not save it to one of your lists.
Log in to save this article

Abstract

Background The TALAPRO-2 trial demonstrated that the combination of talazoparib and enzalutamide significantly improved both progression-free survival (PFS) and overall survival in patients with metastatic castration-resistant prostate cancer (mCRPC). However, the cost-effectiveness of this regimen remains unclear due to its high cost. This study aims to evaluate the cost-effectiveness of this combination compared to enzalutamide monotherapy as a first-line treatment for mCRPC. Methods Based on data from the TALAPRO-2 trial, a dynamic Markov model was constructed to simulate disease progression in mCRPC patients. From the perspectives of US and Chinese payers, total costs, quality-adjusted life years (QALYs), and incremental cost-effectiveness ratios (ICER) were considered as the primary outputs in the model. One-way sensitivity analysis and probabilistic sensitivity analysis were used to validate the robustness of the model. Price reduction analysis provides an evidence-based basis for drug pricing and health insurance negotiations by quantifying the impact of price adjustments on economics. Results In the baseline analysis, the ICERs for talazoparib plus enzalutamide were $646,743.72/QALY and $57,635.76/QALY from the U.S. and China perspectives, respectively, which were above the willingness-to-pay thresholds ($150,000 in the U.S. and $40,334 in China). Sensitivity analyses showed that PFS utility values and drug prices impacted the results most. Price adjustment scenarios showed that China needed a 34.5% price reduction to achieve affordability, whereas the U.S. remained unaffordable even with an 80% price reduction. Conclusion At current pricing, talazoparib plus enzalutamide is not cost-effective for mCRPC patients. Optimizing its economic viability may be possible through genetic testing to screen for HRR mutation-positive populations or price negotiations to reduce drug costs. The study supports differentiated pricing strategies to balance clinical benefits with the rational allocation of healthcare resources.

Article activity feed