Beyond Osimertinib: The Development of Third-Generation EGFR Tyrosine Kinase Inhibitors For Advanced EGFR+ NSCLC
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Single-agent osimertinib is the standard of care for the first-line treatment of advanced EGFR + NSCLC and remained the only marketed third-generation EGFR tyrosine kinase inhibitor (TKI) until March 2020 when almonertinib (HS-10296) was approved in the People's Republic of China for the treatment of advanced EGFR T790M+ NSCLC based on a phase 2 expansion study of a phase 1/2 trial. In this review, we profiled many of the third-generation EGFR TKIs in late-stage clinical development (e.g., almonertinib, lazertinib, alflutinib 1 1The name of ‘Alflutinib' was changed as per the requirements of the National Pharmacopoeia Committee of China and the "China drug generic naming principle", and the name of the drug has been changed from ‘Alflutinib' to ‘Furmonertinib'., rezivertinib, ASK120069, SH-1028, D-0316, and abivertinib) based on their interim results from phase 1 and phase 2 trials, and included the designs of the phase 3 trials and their chemical structures when publicly available. We also listed other third-generation EGFR TKIs in pipeline development based on the search of clinical trial registration websites. In addition, we summarized the results of clinical trials that previously reported third-generation EGFR TKIs (rociletinib, olmutinib, nazartinib, mavelertinib), including phase 3 results of rociletinib and naquotinib. We further profiled combination clinical trial design of the third-generation EGFR TKIs including FLAURA2 (NCT04035486), MARIPOSA (NCT04487080), ACROSS1 (NCT04500704), and ACROSS2 (NCT04500717) that if positive can potentially usher in the next standard of care for advanced EGFR+ NSCLC.
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A positive correlation between drug exposure and dose was observed for lazertinib, and no dose-limiting toxicity.
“A positive correlation between drug exposure and dose was observed, and no dose-limiting toxicity.142–145”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [142]
Oritinib overcomes T790M-mediated drug resistance in NSCLC and inhibits WT-EGFR, EGFRL858R, EGFRL861Q, EGFRL858R/T790M, EGFRd746-750, and EGFRd746-750/T790M kinases, with IC50 values of 18, 0.7, 4, 0.1, 1.4, and 0.89 nM, respectively.
“Oritinib overcomes T790M-mediated drug resistance in NSCLC and inhibits WT-EGFR, EGFRL858R, EGFRL861Q, EGFRL858R/T790M, EGFRd746-750, and EGFRd746-750/T790M kinases. IC50 were 18, 0.7, 4, 0.1, 1.4 and 0.89 nM, respectively.”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [142]
Oritinib binds irreversibly to EGFR kinase by covalently bonding to Cys797 residues targeting ATP binding sites.
“Oritinib binds irreversibly to EGFR kinase by covalently bonding to form Cys797 residues targeting ATP binding sites.”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [142]
Oritinib effectively and selectively targets mutated EGFR cell lines in vitro.
“Oritinib effectively and selectively targets mutated EGFR cell lines in vitro.142,163–165”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [142]
Rezivertinib selectively inhibits the proliferation of EGFR mutated cells in cell lines.
“Rezivertinib selectively inhibits the proliferation of EGFR mutated cells in cell lines.142,169–171”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [142]
MK-8242 (SCH900242) is a potent inhibitor of MDM2 that prevents the interaction between HDM2 and p53, thereby rescuing p53 function.
“MK-8242 (SCH900242) (142), developed by Merck, is a potent inhibitor of MDM2 that prevents the interaction between HDM2 and p53, thereby rescuing p53 function.”
From Recent advances in targeting the “undruggable” proteins: from drug discovery to clinical trials (2023) · cites this paper as [142]
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References 82 · Cited by 219
- Authors
- Nagasaka, M., Zhu, V. W., Lim, S. M., Greco, M., Wu, F., & Ou, S.-H. I.
- Affiliations
- St. Marianna University School of Medicine (JP)
- University of California, Irvine (US)
- Yonsei University (KR)
- Tongji University (CN)
- Corresponding author
- Ou, Sai-Hong Ignatius
- Venue
- Journal of Thoracic Oncology
- Publisher
- Elsevier BV
- Published
- 2021-05
- Volume
- 16
- Issue
- 5
- Pages
- 740-763
- ISSN
- 1556-0864 (ISSN-L)
- OpenAlex
- W3112025484
- Cited by
- 219
- References
- 82
- Citations by year
- 2026: 22 · 2025: 41 · 2024: 37 · 2023: 38 · 2022: 63 · 2021: 18
- FWCI
- 4.31
- Type
- journal article
- Language
- en
- Open access
- hybrid
- doi.org
- Licence
- Locations
- Journal of Thoracic Oncology (publishedVersion, cc-by-nc-nd)
- PubMed (publishedVersion)
- YUHSpace (Yonsei University Medical Library) (submittedVersion, cc-by-nc-nd)
- Topics
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Treatments and Mutations
- Health Sciences › Medicine › Oncology › HER2/EGFR in Cancer Research
- Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Lung Cancer Diagnosis and Treatment
- Keywords
- third-generation EGFR tyrosine kinase inhibitors, EGFR-mutant non-small cell lung cancer, osimertinib, almonertinib, lazertinib, furmonertinib, T790M mutation, rociletinib, combination therapy, phase 3 trial design, drug development pipeline
- MeSH terms
- Acrylamides, Aniline Compounds, China, Humans, Indoles, Lung Neoplasms, Morpholines, Mutation, Pyrazoles, Pyrimidines, Clinical Trials, Phase I as Topic, Clinical Trials, Phase II as Topic, Protein Kinase Inhibitors, ErbB Receptors
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