Table 1.
Overview of data from trials exploring approved antiangiogenic mAbs plus EGFR-TKI combinations for the treatment of aNSCLC with activating EGFR mutations
Name of the trial
(number of patients) |
Phase of the trial | Experimental arm | Control arm | Efficacy data in months |
BELIEF (n = 109) |
II | Erlotinib + bevacizumab | / | mPFS: 13.2 |
JO25567 (n = 154) |
II | Erlotinib + bevacizumab | Erlotinib | mPFS: 16.4 vs. 9.8 (HR: 0.54) mOS: 47.0 vs. 47.4 (HR: 0.81; P = 0.3267) |
NEJ026 (n = 228) |
III | Erlotinib + bevacizumab | Erlotinib | mPFS: 16.9 vs. 13.3 (HR: 0.60) mOS: 50.7 vs. 46.2 (HR: 1.007; P = 0.97) |
BEVERLY (n = 160) |
III | Erlotinib + bevacizumab | Erlotinib | mPFS: 15.4 vs. 9.7 (HR: 0.60) mOS: 28.4 vs. 23.0 (HR: 0.70; P = 0.12) |
ARTEMIS-CTONG1509 (n = 311) |
III | Erlotinib + bevacizumab | Erlotinib | mPFS: 17.9 vs. 11.2 (HR: 0.55) mOS: 36.2 vs. 31.6 (HR: 0.92; P = 0.581) |
RELAY (n = 449) |
III | Erlotinib + ramucirumab | Erlotinib | mPFS: 19.4 vs. 12.4 (HR: 0.59) |
EGFR-TKI: Epidermal growth factor receptor-tyrosine kinase inhibitor; NSCLC: non-small cell lung cancer; HR: hazard ratio.