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. 2025 Nov 17;19:2037. doi: 10.3332/ecancer.2025.2037

Table 3. Efficacy, safety and development status of targeted therapies for EGFR exon20ins–mutant NSCLC [12, 36, 41, 42].

Drug (Trial identifier) Type ORR (%) Median PFS (months) CNS Activity Route Key AEs (≥ Grade 3) Development Status
Amivantamab (NCT02609776) Bispecific EGFR-MET monoclonal antibody 40 8.3 Limited IV infusion Rash (4%), IRR (3%), Paronychia (1%) FDA-approved; ongoing phase III trials
Mobocertinib (NCT02716116) Oral EGFR TKI 28 7.3 Limited Oral Diarrhea (16%), QTc prolongation (3%) Withdrawn from market (2023)
Sunvozertinib (NCT05712902) Oral EGFR TKI (3rd-gen, irreversible) 61 7.6 Promising Oral Blood creatine Phosphokinase increased (17%), Diarrhea (8%), Anemia(6%) In development; ongoing trials
Poziotinib (NCT03318939) Oral EGFR/HER2 TKI 27.8 5.5 Limited Oral Rash (48%), Diarrhea (25%), Stomatitis (24%) Development discontinued

EGFR = Epidermal Growth Factor Receptor; NSCLC = Non–Small Cell Lung Cancer; ORR = Objective Response Rate; PFS = Progression-Free Survival; CNS = Central Nervous System; IV = Intravenous; IRR = Infusion-Related Reaction; TKI = Tyrosine Kinase Inhibitor

Adverse events (AEs) reported are grade ≥3 where available. Data are derived from single-arm clinical trials unless otherwise specified. Trial identifiers (NCT numbers) correspond to ClinicalTrials.gov registry entries.

Note: Mobocertinib data are based on the original EXCLAIM trial (NCT02716116) in previously treated patients; data from EXCLAIM-2 are not included in this table. Original table