Efficacy of Immune Checkpoint Inhibitors vs. Tyrosine Kinase Inhibitors/Everolimus in Adjuvant Renal Cell Carcinoma: Indirect Comparison of Disease-Free Survival

Author:

Ossato Andrea1ORCID,Gasperoni Lorenzo2ORCID,Del Bono Luna3,Messori Andrea4ORCID,Damuzzo Vera56

Affiliation:

1. Department of Pharmaceutical and Pharmacological Sciences, University of Padua, 35131 Padova, Italy

2. Oncological Pharmacy Unit, IRCCS Istituto Romagnolo per lo Studio dei Tumori (IRST) “Dino Amadori”, 47014 Meldola, Italy

3. Azienda Ospedaliera Universitaria Pisana, 56100 Pisa, Italy

4. HTA Unit, Regional Health Service, 50139 Florence, Italy

5. Hospital Pharmacy, Vittorio Veneto Hospital, 31029 Vittorio Veneto, Italy

6. Italian Society of Clinical Pharmacy and Therapeutics (SIFaCT), 10123 Turin, Italy

Abstract

Background: The proven efficacy of mTOR inhibitors (mTORIs), tyrosine kinase inhibitors (TKIs) or immune checkpoint inhibitors (ICIs) in metastatic renal cell carcinoma (RCC) suggests that these agents should be investigated as adjuvant therapy with the aim of eliminating undetectable microscopic residual disease after curative resection. The aim of our study was to compare the efficacy of these treatments using an innovative method of reconstructing individual patient data. Methods: Nine phase III trials describing adjuvant RCC treatments were selected. The IPDfromKM method was used to reconstruct individual patient data from Kaplan–Meier (KM) curves. The combination treatments were compared with the control arm (placebo) for disease-free survival (DFS). Multi-treatment KM curves were used to summarize the results. Standard statistical tests were performed. These included hazard ratio and likelihood ratio tests for heterogeneity. Results: In the overall population, the study showed that two ICIs (nivolumab plus ipilimumab and pembrolizumab) and one TKI (sunitinib) were superior to the placebo, whereas both TKIs and mTORIs were inferior. As we assessed DFS as the primary endpoint for the adjuvant comparison, the overall survival benefit remains unknown. Conclusions: This novel approach to investigating survival has allowed us to conduct all indirect head-to-head comparisons between these agents in a context where no “real” comparative trials have been conducted.

Publisher

MDPI AG

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