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Ultra-Fast Amplicon-Based Next-Generation Sequencing in Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
[Advances in neoadjuvant therapy for EGFR-mutant non-small cell lung cancer]
1Department of Respiratory and Critical Care Medicine, Shanghai Chest Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai 200030, China.
Abstract:
Epidermal growth factor receptor (EGFR) mutation is the most common driver mutation in non-small cell lung cancer (NSCLC) among Asian populations. For patients with resectable EGFR-mutant NSCLC, the high risk of postoperative recurrence remains a major clinical challenge. The neoadjuvant treatment paradigm has shifted from conventional chemotherapy to precision therapies centered on EGFR-tyrosine kinase inhibitors (TKIs), aiming to downstage tumor and eradicate micrometastases before surgery, thereby improving surgical outcomes and long-term survival. This article systematically reviews the evolution and recent advances in neoadjuvant therapy for EGFR-mutant NSCLC. As of December 2025, osimertinib-based regimens, whether used as monotherapy or in combination with chemotherapy, have emerged as potential options in this field and are supported by high-level evidence-based medicine. The article also discusses the limitations of immunotherapy in the EGFR-mutant NSCLC population and the future development trends of combination strategies, emphasizing that biomarker-guided individualized therapy represents the corner direction moving forward.
Insights
Neoadjuvant EGFR-tyrosine kinase inhibitors (TKIs) are revolutionizing treatment for non-small cell lung cancer (NSCLC) with EGFR mutations. Osimertinib-based therapies show promise in preventing recurrence after surgery.
Area of Science:
- Oncology
- Medical Research
Background:
- Epidermal growth factor receptor (EGFR) mutations are prevalent in non-small cell lung cancer (NSCLC), particularly in Asian populations.
- High recurrence rates post-surgery for resectable EGFR-mutant NSCLC present a significant clinical challenge.
- Neoadjuvant therapy has evolved from chemotherapy to targeted EGFR-tyrosine kinase inhibitors (TKIs) to improve outcomes.
Purpose of the Study:
- To systematically review the evolution and recent advancements in neoadjuvant therapy for EGFR-mutant NSCLC.
- To highlight the role of precision therapies in the neoadjuvant setting.
- To discuss future directions in treatment strategies.
Main Methods:
- Systematic literature review of neoadjuvant therapies for EGFR-mutant NSCLC.
- Analysis of clinical trial data and evidence-based medicine regarding TKI efficacy.
- Evaluation of current and emerging treatment paradigms.
Main Results:
- Osimertinib-based regimens (monotherapy or combination) are emerging as promising neoadjuvant options for EGFR-mutant NSCLC.
- These regimens are supported by high-level evidence and aim to improve surgical outcomes and survival.
- Immunotherapy shows limitations in this specific patient population.
Conclusions:
- Neoadjuvant osimertinib-based therapies represent a significant advancement for EGFR-mutant NSCLC.
- Future strategies will likely focus on combination therapies and biomarker-guided individualized treatment.
- Personalized medicine is the future direction for managing EGFR-mutant NSCLC.
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