Table 2.
Study | Treatment | Patients (n) | Clinical outcome (months) | p valuea |
---|---|---|---|---|
Subgroup with uncommon EGFR mutationsb | ||||
South Korea | ||||
Kim et al. [30] | Afatinib | 14 | PFS: not reached | 0.06 |
Gefitinib | 12 | PFS: 5.0 | ||
Erlotinib | 5 | PFS: 6.1 | ||
Taiwan | ||||
Lin et al. [32] | Afatinib | 17 | OS: 38.6 | 0.81 |
Gefitinib | 10 | OS: not reached | ||
Erlotinib | 4 | OS: 33.6 | ||
Shen et al. [44] | Afatinib | 24 | PFS: 11.0c | 0.03 |
Gefitinib | 32 (combined) | PFS: 3.6 (combined) | ||
Erlotinib | ||||
Tu et al. [34] | Afatinib | 23 | PFS: 19.7 | 0.506 |
Gefitinib | 14 | PFS: 7.0 | ||
Erlotinib | 12 | PFS: 7.0 | ||
Yang et al. [74] | Afatinib | 17 | PFS: 5.5 | 0.3025 |
Gefitinib | 31 | PFS: 6.2 | ||
Erlotinib | 9 | PFS: 9.0 | ||
Subgroup with brain metastases at baseline | ||||
South Korea | ||||
Kim et al.d [30] | Afatinib only | 71 (combined) | PFS: 15.7 | 0.21 |
Afatinib + WBRT | PFS: 11.5 | |||
Afatinib + GKS | PFS: 15.6 | |||
Taiwan | ||||
Kuan et al. [31] | Afatinib | 17 | PFS | HR: 0.42 (95% CI 0.16–1.05)e |
Gefitinib | 60 | |||
Erlotinib | 11 | |||
Su et al. [54] | Afatinib | NRf | PFS: 8.2 | 0.34 |
Gefitinib | PFS: 10.5 | |||
Erlotinib | PFS: 10.4 | |||
Tu et al. [34] | Afatinib | 22 | PFS: 9.9 | 0.367 |
Gefitinib | 34 | PFS: 8.9 | ||
Erlotinib | 17 | PFS: 7.2 |
CI confidence interval, EGFR epidermal growth factor receptor, GKS gamma knife surgery, HR hazard ratio, NR not reported, NSCLC non-small cell lung cancer, OS overall survival, PFS progression-free survival, TKIs tyrosine kinase inhibitors, WBRT whole brain radiotherapy
aAfatinib versus comparator(s)
bEGFR mutations other than Del19 or L858R
cExcluded patients with EGFR exon 20 insertions
dData for gefitinib and erlotinib not reported
eHR for afatinib versus gefitinib
fOverall, 115, 116, and 75 patients received afatinib, gefitinib, and erlotinib, respectively; however, the number of patients with brain metastases at baseline was not reported