TY - JOUR
T1 - Two-year survival with nivolumab in previously treated advanced non–small-cell lung cancer
T2 - A real-world pooled analysis of patients from France, Germany, and Canada
AU - Debieuvre, Didier
AU - Juergens, Rosalyn A.
AU - Asselain, Bernard
AU - Audigier-Valette, Clarisse
AU - Auliac, Jean Bernard
AU - Barlesi, Fabrice
AU - Benoit, Nicolas
AU - Bombaron, Pierre
AU - Butts, Charles A.
AU - Dixmier, Adrien
AU - Gröschel, Andreas
AU - Gutz, Sylvia
AU - Labbé, Catherine
AU - Moro-Sibilot, Denis
AU - Pérol, Maurice
AU - Raspaud, Christophe
AU - Schumann, Christian
AU - Juarez-Garcia, Ariadna
AU - Lakhdari, Khalid
AU - Pettersson, Filippa
AU - Penrod, John R.
AU - Reynaud, Dorothee
AU - Waldenberger, Daniela
AU - Allan, Victoria
AU - Sebastian, Martin
N1 - Publisher Copyright:
© 2021 Bristol Myers Squibb
PY - 2021/7/1
Y1 - 2021/7/1
N2 - Objectives: Immune checkpoint inhibitors have become the standard of care for metastatic non–small-cell lung cancer (NSCLC) progressing during or after platinum-based chemotherapy. Real-world clinical practice tends to represent more diverse patient characteristics than randomized clinical trials. We sought to evaluate overall survival (OS) outcomes in the total study population and in key subsets of patients who received nivolumab for previously treated advanced NSCLC in real-world settings in France, Germany, or Canada. Materials and methods: Data were pooled from two prospective observational cohort studies, EVIDENS and ENLARGE, and a retrospective registry in Canada. Patients included in this analysis were aged ≥18 years, had stage IIIB/IV NSCLC, and received nivolumab after at least one prior line of systemic therapy. OS was estimated in the pooled population and in various subgroups using the Kaplan-Meier method. Timing of data collection varied across cohorts (2015–2019). Results: Of the 2585 patients included in this analyses, 1235 (47.8 %) were treated in France, 881 (34.1 %) in Germany, and 469 (18.1 %) in Canada. Median OS for the total study population was 11.3 months (95 % CI: 10.5–12.2); this was similar across France, Germany, and Canada. The OS rate was 49 % at 1 year and 28 % at 2 years for the total study population. In univariable Cox analyses, the presence of epidermal growth factor receptor mutations in nonsquamous disease, liver, or bone metastases were associated with significantly shorter OS, whereas tumor programmed death ligand 1 expression and Eastern Cooperative Oncology Group performance status 0–1 were associated with significantly prolonged OS. Similar OS was noted across subgroups of age and prior lines of therapy. Conclusion: OS rates in patients receiving nivolumab for previously treated advanced NSCLC in real-world clinical practice closely mirrored those in phase 3 studies, suggesting similar effectiveness of nivolumab in clinical trials and clinical practice.
AB - Objectives: Immune checkpoint inhibitors have become the standard of care for metastatic non–small-cell lung cancer (NSCLC) progressing during or after platinum-based chemotherapy. Real-world clinical practice tends to represent more diverse patient characteristics than randomized clinical trials. We sought to evaluate overall survival (OS) outcomes in the total study population and in key subsets of patients who received nivolumab for previously treated advanced NSCLC in real-world settings in France, Germany, or Canada. Materials and methods: Data were pooled from two prospective observational cohort studies, EVIDENS and ENLARGE, and a retrospective registry in Canada. Patients included in this analysis were aged ≥18 years, had stage IIIB/IV NSCLC, and received nivolumab after at least one prior line of systemic therapy. OS was estimated in the pooled population and in various subgroups using the Kaplan-Meier method. Timing of data collection varied across cohorts (2015–2019). Results: Of the 2585 patients included in this analyses, 1235 (47.8 %) were treated in France, 881 (34.1 %) in Germany, and 469 (18.1 %) in Canada. Median OS for the total study population was 11.3 months (95 % CI: 10.5–12.2); this was similar across France, Germany, and Canada. The OS rate was 49 % at 1 year and 28 % at 2 years for the total study population. In univariable Cox analyses, the presence of epidermal growth factor receptor mutations in nonsquamous disease, liver, or bone metastases were associated with significantly shorter OS, whereas tumor programmed death ligand 1 expression and Eastern Cooperative Oncology Group performance status 0–1 were associated with significantly prolonged OS. Similar OS was noted across subgroups of age and prior lines of therapy. Conclusion: OS rates in patients receiving nivolumab for previously treated advanced NSCLC in real-world clinical practice closely mirrored those in phase 3 studies, suggesting similar effectiveness of nivolumab in clinical trials and clinical practice.
KW - Nivolumab
KW - Non–small-cell lung cancer
KW - Observational study
KW - Overall survival
KW - Real-world data
UR - http://www.scopus.com/inward/record.url?scp=85105570062&partnerID=8YFLogxK
U2 - 10.1016/j.lungcan.2021.04.022
DO - 10.1016/j.lungcan.2021.04.022
M3 - Article
C2 - 33980420
AN - SCOPUS:85105570062
SN - 0169-5002
VL - 157
SP - 40
EP - 47
JO - Lung Cancer
JF - Lung Cancer
ER -