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Updated: Jan 27, 2026

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Published on: September 28, 2009
Abstract:
Patients with EGFR-mutant non-small cell lung cancer who develop MET-driven resistance to an EGFR inhibitor-be it a first-, second-, or third-generation drug-stand to benefit from follow-up treatment with a combination of EGFR-targeted osimertinib and MET-blocking savolitinib, according to an interim analysis of two expansion cohorts from the multiarm TATTON trial.
Insights
Patients with EGFR-mutant non-small cell lung cancer resistant to EGFR inhibitors may benefit from a combination of osimertinib and savolitinib. This combination targets both EGFR and MET pathways, offering a new treatment strategy.
Area of Science:
- Oncology
- Pharmacology
Background:
- Non-small cell lung cancer (NSCLC) with EGFR mutations is often treated with EGFR inhibitors.
- Acquired resistance to EGFR inhibitors, particularly MET-driven resistance, is a significant clinical challenge.
Discussion:
- The TATTON trial's interim analysis suggests a potential benefit of combining osimertinib (EGFR inhibitor) with savolitinib (MET inhibitor).
- This combination therapy addresses MET-driven resistance mechanisms that emerge after treatment with various generations of EGFR inhibitors.
Key Insights:
- Patients with EGFR-mutant NSCLC developing MET-driven resistance can respond to sequential treatment with osimertinib and savolitinib.
- The combination targets both the primary EGFR mutation and secondary MET alterations driving resistance.
Outlook:
- This combination strategy may represent a new therapeutic option for NSCLC patients who have progressed on prior EGFR-targeted therapies.
- Further investigation and long-term data from the TATTON trial are warranted to confirm efficacy and safety.
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