Evaluation of Major Pathologic Response and Pathologic Complete Response as Surrogate End Points for Survival in Randomized Controlled Trials of Neoadjuvant Immune Checkpoint Blockade in Resectable in NSCLC

Authors

Jacobi B Hines
Robert B Cameron
Alessandra Esposito
Leeseul Kim
Luca Porcu
Antonio Nuccio
Giuseppe Viscardi
Roberto Ferrara
Giulia Veronesi
Patrick M Forde
Janis Taube
Everett Vokes
Christine M Bestvina
James M Dolezal
Matteo Sacco
Marta Monteforte
Tina Cascone
Marina C Garassino
Valter Torri

Publication Date

7-1-2024

Journal

Journal of Thoracic Oncology

DOI

10.1016/j.jtho.2024.03.010

PMID

38461929

Abstract

Introduction: Controversy remains as to whether pathologic complete response (pCR) and major pathologic response (MPR) represent surrogate end points for event-free survival (EFS) and overall survival (OS) in neoadjuvant trials for resectable NSCLC.

Methods: A search of PubMed and archives of international conference abstracts was performed from June 2017 through October 31, 2023. Studies incorporating a neoadjuvant arm with immune checkpoint blockade alone or in combination with chemotherapy were included. Those not providing information regarding pCR, MPR, EFS, or OS were excluded. For trial-level surrogacy, log ORs for pCR and MPR and log hazard ratios for EFS and OS were analyzed using a linear regression model weighted by sample size. The regression coefficient and R2 with 95% confidence interval were calculated by the bootstrapping approach.

Results: Seven randomized clinical trials were identified for a total of 2385 patients. At the patient level, the R2 of pCR and MPR with 2-year EFS were 0.82 (0.66-0.94) and 0.81 (0.63-0.93), respectively. The OR of 2-year EFS rates by response status was 0.12 (0.07-0.19) and 0.11 (0.05-0.22), respectively. For the 2-year OS, the R2 of pCR and MPR were 0.55 (0.09-0.98) and 0.52 (0.10-0.96), respectively. At the trial level, the R2 for the association of OR for response and HR for EFS was 0.58 (0.00-0.97) and 0.61 (0.00-0.97), respectively.

Conclusions: Our analyses reveal a robust correlation between pCR and MPR with 2-year EFS but not OS. Trial-level surrogacy was moderate but imprecise. More mature follow-up and data to assess the impact of study crossover are needed.

Keywords

Humans, Carcinoma, Non-Small-Cell Lung, Immune Checkpoint Inhibitors, Lung Neoplasms, Neoadjuvant Therapy, Pathologic Complete Response, Randomized Controlled Trials as Topic, Survival Rate, Chemoimmunotherapy, Immunotherapy, NSCLC, Neoadjuvant, Pathologic response, Surrogate end points

Published Open-Access

yes

Recommended Citation

Hines, Jacobi B; Cameron, Robert B; Esposito, Alessandra; et al., "Evaluation of Major Pathologic Response and Pathologic Complete Response as Surrogate End Points for Survival in Randomized Controlled Trials of Neoadjuvant Immune Checkpoint Blockade in Resectable in NSCLC" (2024). Faculty, Staff and Student Publications. 4282.
https://digitalcommons.library.tmc.edu/uthgsbs_docs/4282