Table 1. summary of the rate of patients who received post-progression systemic treatments in clinical trials with EGFR-TKIs.
Study | EGFR-TKI | Post-progression treatment*, % |
---|---|---|
IPASS, Fukuoka et al., J Clin Oncol 2011 | Gefitinib | 76 |
NEJ002, Inoue et al., Ann Oncol 2013 | Gefitinib | 72 |
WJTOG 3405, Yoshioka et al., Ann Oncol 2019 | Gefitinib | 86 |
EURTAC, Rosell et al., Lancet Oncol 2012 | Erlotinib | 68 |
OPTIMAL, Zhou et al., Ann Oncol 2015 | Erlotinib | 63 |
LUX-LUNG 3, Yang et al., Lancet Oncol 2015 | Afatinib | 71 |
LUX-LUNG 6, Yang et al., Lancet Oncol 2015 | Afatinib | 57 |
LUX-LUNG 7, Paz-Ares et al., Ann Oncol 2017 | Afatinib | 73 |
Gefitinib | 77 | |
FLAURA, Ramalingam et al., N Engl J Med 2020 | Osimertinib | 60 |
Erlotinib/gefitinib | 68 |
*, After discontinuation of study treatment, excludes patients remaining on assigned treatment at data cut-off, pre-progression treatment and death. EGFR-TKI, epidermal growth factor receptor-tyrosine kinase inhibitor.