Pathological response in resectable non–small cell lung cancer: a systematic literature review and meta-analysis

Author:

Waser Nathalie A1ORCID,Quintana Melanie2,Schweikert Bernd3,Chaft Jamie E4,Berry Lindsay2,Adam Ahmed1,Vo Lien5,Penrod John R5,Fiore Joseph5,Berry Donald A2,Goring Sarah1

Affiliation:

1. Insights, Evidence and Value, ICON plc , Burlington, ON, Canada

2. Berry Consultants LCC , Houston, TX, USA

3. Insights, Evidence and Value, ICON plc , Munich, Germany

4. Department of Medicine, Memorial Sloan Kettering Cancer Center , New York, NY, USA

5. Health Economics and Outcomes Research, Bristol Myers Squibb , Lawrenceville, NJ, USA

Abstract

Abstract Background Surrogate endpoints for overall survival in patients with resectable non–small cell lung cancer receiving neoadjuvant therapy are needed to provide earlier treatment outcome indicators and accelerate drug approval. This study’s main objectives were to investigate the association among pathological complete response, major pathological response, event-free survival and overall survival and to determine whether treatment effects on pathological complete response and event-free survival correlate with treatment effects on overall survival. Methods A comprehensive systematic literature review was conducted to identify neoadjuvant studies in resectable non–small cell lung cancer. Analysis at the patient level using frequentist and Bayesian random effects (hazard ratio [HR] for overall survival or event-free survival by pathological complete response or major pathological response status, yes vs no) and at the trial level using weighted least squares regressions (hazard ratio for overall survival or event-free survival vs pathological complete response, by treatment arm) were performed. Results In both meta-analyses, pathological complete response yielded favorable overall survival compared with no pathological complete response (frequentist, 20 studies and 6530 patients: HR = 0.49, 95% confidence interval = 0.42 to 0.57; Bayesian, 19 studies and 5988 patients: HR = 0.48, 95% probability interval = 0.43 to 0.55) and similarly for major pathological response (frequentist, 12 studies and 1193 patients: HR = 0.36, 95% confidence interval = 0.29 to 0.44; Bayesian, 11 studies and 1018 patients: HR = 0.33, 95% probability interval = 0.26 to 0.42). Across subgroups, estimates consistently showed better overall survival or event-free survival in pathological complete response or major pathological response compared with no pathological complete response or no major pathological response. Trial-level analyses showed a moderate to strong correlation between event-free survival and overall survival hazard ratios (R2 = 0.7159) but did not show a correlation between treatment effects on pathological complete response and overall survival or event-free survival. Conclusion There was a strong and consistent association between pathological response and survival and a moderate to strong correlation between event-free survival and overall survival following neoadjuvant therapy for patients with resectable non–small cell lung cancer.

Funder

Bristol Myers Squibb

Publisher

Oxford University Press (OUP)

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