Abstract

Background: Recent randomized controlled trials have demonstrated that immune checkpoint inhibitors (ICIs) improve patient outcomes, but whether these novel agents are cost-effective for untreated advanced renal cell carcinoma (aRCC) remains unclear.Materials and Methods: A microsimulation model was created to project the healthcare costs and outcomes of six strategies (lenvatinib-plus-pembrolizumab, nivolumab-plus-cabozantinib, nivolumab-plus-ipilimumab, pembrolizumab-plus-axitinib, avelumab-plus-axitinib, and sunitinib monotherapy) for patients with aRCC. Transition probability of patients was estimated from CLEAR, CheckMate 9ER, CheckMate 214, KEYNOTE-426, JAVELIN Renal 101, and other data sets by using parametric survival modeling. Lifetime direct medical costs, life years (LYs), quality-adjusted LYs (QALYs), and incremental cost-effectiveness ratios (ICERs) were estimated from a United States payer perspective. One-way and probabilistic sensitivity analyses were performed, along with multiple scenario analyses, to evaluate model uncertainty.Results: Of the six competing strategies, nivolumab-plus-cabozantinib yielded the most significant health outcomes, and the sunitinib strategy was the least expensive option. The cost-effective frontier consisted of the nivolumab-plus-cabozantinib, pembrolizumab-plus-axitinib, and sunitinib strategies, which displayed the ordered ICERs of $81282/QALY for pembrolizumab-plus-axitinib vs sunitinib and $453391/QALY for nivolumab-plus-cabozantinib vs pembrolizumab-plus-axitinib. The rest of the strategies, such as lenvatinib-plus-pembrolizumab, nivolumab-plus-ipilimumab, and avelumab-plus-axitinib, were dominated. The cost of sunitinib drove the model most influentially.Conclusions: For aRCC, the pembrolizumab-plus-axitinib strategy is likely to be the most cost-effective alternative at the willingness-to-pay threshold of $100,000.

Highlights

  • Renal cell carcinoma (RCC) is the most common type of kidney cancer, with more than 73,000 cases diagnosed and 14,000 deaths in 2020 in the United States (Choueiri et al, 2015; National Cancer Institute, 2021)

  • The cost-effective frontier consisted of the nivolumab-plus-cabozantinib, pembrolizumabplus-axitinib, and sunitinib strategies, which displayed the ordered incremental cost-effectiveness ratios (ICERs) of $81282/ quality-adjusted LYs (QALYs) for pembrolizumab-plus-axitinib vs sunitinib and $453391/QALY for nivolumabplus-cabozantinib vs pembrolizumab-plus-axitinib

  • We developed the final scenario analysis accommodating indicationspecific pricing, where the cost of nivolumab used in combination with cabozantinib in the first-line treatment varied from the price of nivolumab monotherapy used at second-line setting

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Summary

Introduction

Renal cell carcinoma (RCC) is the most common type of kidney cancer, with more than 73,000 cases diagnosed and 14,000 deaths in 2020 in the United States (Choueiri et al, 2015; National Cancer Institute, 2021). Once the mainstay target drug for the treatment of aRCC, has been substituted by novel immune checkpoint inhibitor (ICI) agents on the basis of survival data reported in multiple previous studies. The proportion of patients with 12-month OS was 85.7% with the nivolumab-plus-cabozantinib strategy vs 75.6% with sunitinib strategy (Choueiri et al, 2021) Another randomized phase three trial (CLEAR) revealed that lenvatinibplus-pembrolizumab showed significant improvement when compared with sunitinib with respect to OS (median, 14.7 vs 9.2 months; HR, 0.65; 95% CI, 0.53–0.80) and PFS (median, 23.9 vs 9.2 months; HR, 0.39; 95% CI, 0.32–0.49) (Motzer et al, 2021). Recent randomized controlled trials have demonstrated that immune checkpoint inhibitors (ICIs) improve patient outcomes, but whether these novel agents are cost-effective for untreated advanced renal cell carcinoma (aRCC) remains unclear

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