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A Detouring Experience Not Recommended: Lessons Learned from PF00299804
Molly Li1,2, Kevin Mok3, Tony Mok1,2
1Department of Clinical Oncology, The Chinese University of Hong Kong, Hong Kong.
Abstract:
Patients with mutant EGFR positive non-small cell lung cancer (NSCLC) benefit from tyrosine kinase inhibitor (TKI) treatment. However, all patients ultimately develop acquired resistance, half of which are attributed to the EGFR exon 20 T790M mutation. A landmark publication in Cancer Research in 2007 demonstrated improved drug potency and pan-human EGFR (HER) inhibition with PF00299804, a second-generation EGFR TKI. Compared with first-generation EGFR TKI, PF00299804 showed the ability to overcome T790M mutation in vitro and had the potential to improve treatment outcomes of patients with mutant EGFR-positive NSCLC. Here we review the preclinical and clinical development of PF00299804 and reflect on the lessons learned from this detouring experience. See related article by Engelman and colleagues, Cancer Res 2007;67:11924-32.
Insights
Second-generation EGFR TKI PF00299804 demonstrated potent inhibition and ability to overcome T790M resistance mutations in preclinical models. This review examines its development and lessons learned for non-small cell lung cancer (NSCLC) treatment.
Area of Science:
- Oncology
- Pharmacology
- Molecular Biology
Background:
- Non-small cell lung cancer (NSCLC) patients with mutant EGFR benefit from tyrosine kinase inhibitors (TKIs).
- Acquired resistance, often due to the EGFR exon 20 T790M mutation, limits TKI efficacy.
- Second-generation EGFR TKIs aim to overcome resistance mechanisms.
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