Five-year survival outcomes from the PACIFIC trial: Durvalumab after chemoradiotherapy in stage III non-small-cell lung cancer Journal Article


Authors: Spigel, D. R.; Faivre-Finn, C.; Gray, J. E.; Vicente, D.; Planchard, D.; Paz-Ares, L.; Vansteenkiste, J. F.; Garassino, M. C.; Hui, R.; Quantin, X.; Rimner, A.; Wu, Y. L.; Özgüroğlu, M.; Lee, K. H.; Kato, T.; de Wit, M.; Kurata, T.; Reck, M.; Cho, B. C.; Senan, S.; Naidoo, J.; Mann, H.; Newton, M.; Thiyagarajah, P.; Antonia, S. J.; on behalf of the PACIFIC Investigators
Article Title: Five-year survival outcomes from the PACIFIC trial: Durvalumab after chemoradiotherapy in stage III non-small-cell lung cancer
Abstract: PURPOSE The phase III PACIFIC trial compared durvalumab with placebo in patients with unresectable, stage III non-small-cell lung cancer and no disease progression after concurrent chemoradiotherapy. Consolidation durvalumab was associated with significant improvements in the primary end points of overall survival (OS; stratified hazard ratio [HR], 0.68; 95% CI, 0.53 to 0.87; P=.00251) and progression-free survival (PFS [blinded independent central review; RECIST v1.1]; stratified HR, 0.52; 95% CI, 0.42 to 0.65; P<.0001), with manageable safety. We report updated, exploratory analyses of survival, approximately 5 years after the last patient was randomly assigned. METHODS Patients with WHO performance status 0 or 1 (any tumor programmed cell death-ligand 1 status) were randomly assigned (2:1) to durvalumab (10 mg/kg intravenously; administered once every 2 weeks for 12 months) or placebo, stratified by age, sex, and smoking history. Time-to-event end point analyses were performed using stratified log-rank tests. Medians and landmark survival rates were estimated using the Kaplan-Meier method. RESULTS Seven hundred and nine of 713 randomly assigned patients received durvalumab (473 of 476) or placebo (236 of 237). As of January 11, 2021 (median follow-up, 34.2 months [all patients]; 61.6 months [censored patients]), updated OS (stratified HR, 0.72; 95% CI, 0.59 to 0.89; median, 47.5 v 29.1 months) and PFS (stratified HR, 0.55; 95% CI, 0.45 to 0.68; median, 16.9 v 5.6 months) remained consistent with the primary analyses. Estimated 5-year rates (95% CI) for durvalumab and placebo were 42.9% (38.2 to 47.4) versus 33.4% (27.3 to 39.6) for OS and 33.1% (28.0 to 38.2) versus 19.0% (13.6 to 25.2) for PFS. CONCLUSION These updated analyses demonstrate robust and sustained OS and durable PFS benefit with durvalumab after chemoradiotherapy. An estimated 42.9% of patients randomly assigned to durvalumab remain alive at 5 years and 33.1% of patients randomly assigned to durvalumab remain alive and free of disease progression, establishing a new benchmark for standard of care in this setting. (C) 2022 by American Society of Clinical Oncology
Keywords: cisplatin; radiation; etoposide; docetaxel; phase-iii; concurrent; nsclc; consolidation chemotherapy; real-world data
Journal Title: Journal of Clinical Oncology
Volume: 40
Issue: 12
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2022-04-20
Start Page: 1301
End Page: 1311
Language: English
ACCESSION: WOS:000799692000006
DOI: 10.1200/jco.21.01308
PROVIDER: wos
PMCID: PMC9015199
PUBMED: 35108059
Notes: Article -- Source: Wos
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Andreas Rimner
    524 Rimner