Tackling Osimertinib Resistance in EGFR-Mutant Non-Small Cell Lung Cancer
Juan Bautista Blaquier1, Sandra Ortiz-Cuaran2, Biagio Ricciuti3
1Thoracic Oncology Unit, Medical Oncology, Center for Medical Education and Clinical Research (CEMIC), Buenos Aires, Argentina.
Abstract:
The current landscape of targeted therapies directed against oncogenic driver alterations in non-small cell lung cancer (NSCLC) is expanding. Patients with EGFR-mutant NSCLC can derive significant benefit from EGFR tyrosine kinase inhibitor (TKI) therapy, including the third-generation EGFR TKI osimertinib. However, invariably, all patients will experience disease progression with this therapy mainly due to the adaptation of cancer cells through primary or secondary molecular mechanisms of resistance. The comprehension and access to tissue and cell-free DNA next-generation sequencing have fueled the development of innovative therapeutic strategies to prevent and overcome resistance to osimertinib in the clinical setting. Herein, we review the biological and clinical implications of molecular mechanisms of osimertinib resistance and the ongoing development of therapeutic strategies to overcome or prevent resistance.
Insights
Osimertinib is effective for EGFR-mutant non-small cell lung cancer (NSCLC), but resistance develops. New strategies are emerging to overcome or prevent this resistance, improving patient outcomes.
Area of Science:
- Oncology
- Molecular Biology
- Pharmacology
Background:
- Targeted therapies for non-small cell lung cancer (NSCLC) are advancing, with EGFR tyrosine kinase inhibitors (TKIs) like osimertinib showing efficacy in EGFR-mutant NSCLC.
- Despite initial benefits, acquired resistance to osimertinib inevitably leads to disease progression in patients with EGFR-mutant NSCLC.
Conclusions:
- Understanding osimertinib resistance mechanisms is crucial for developing effective treatment strategies.
- Next-generation sequencing plays a vital role in identifying resistance and guiding therapeutic decisions.
- Innovative combination therapies and novel agents are under development to combat osimertinib resistance in NSCLC.
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