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Updated: May 23, 2025

Establishment and Characterization of Three Afatinib-resistant Lung Adenocarcinoma PC-9 Cell Lines Developed with Increasing Doses of Afatinib
Published on: June 26, 2019
Impact of Modifying Lazertinib Doses on Effectiveness and Safety in Patients With EGFR-Positive Advanced Lung Cancer:
Mi-Hyun Kim1, Min Ki Lee1, Ji Eun Park2
1Department of Internal Medicine, Pusan National University School of Medicine, Busan, Republic of Korea.
Introduction:
The clinical application of lazertinib, a third-generation epidermal growth factor receptor (EGFR) tyrosine kinase inhibitor, has extended to the treatment of EGFR-mutant non-small-cell lung cancer (NSCLC); however, the effects of its dose modification on its efficacy and safety have not yet been adequately established.
Methods:
This prospective, multicenter, observational cohort study aims to evaluate the clinical implications of adjusting the lazertinib dose. Patients will be categorized into two groups based on the lazertinib dose administered during the initial 12 weeks of treatment in routine clinical practice: 160 and 240 mg groups. The primary endpoints are progression-free survival in the 160 mg group and identifying risk factors associated with dose modification during the 12-week period.
Discussion:
The findings from the present study will provide real-world insights into the clinical factors leading to lazertinib dose adjustments and deepen our understanding of the efficacy and safety of lazertinib in patients with NSCLC. Our research will contribute toward optimizing medical strategies for NSCLC treatment and aid clinicians in making accurate clinical decisions regarding dose modifications in routine practice.
Insights
This study investigates lazertinib dose adjustments in non-small-cell lung cancer (NSCLC) patients. It examines how modifying the dose impacts treatment effectiveness and safety in real-world clinical settings.
Area of Science:
- Oncology
- Pharmacology
- Clinical Medicine
Background:
- Lazertinib is a third-generation EGFR tyrosine kinase inhibitor used for EGFR-mutant NSCLC.
- The impact of lazertinib dose modification on efficacy and safety requires further investigation.
Purpose of the Study:
- To evaluate the clinical implications of lazertinib dose adjustments.
- To understand factors influencing dose modification in routine practice.
- To assess the efficacy and safety of different lazertinib doses.
Main Methods:
- Prospective, multicenter, observational cohort study.
- Patients divided into 160 mg and 240 mg lazertinib dose groups.
- Primary endpoints: progression-free survival and risk factors for dose modification within 12 weeks.
Main Results:
- This section is to be filled upon study completion.
Conclusions:
- Study findings will offer real-world insights into lazertinib dose adjustments.
- Enhanced understanding of lazertinib efficacy and safety in NSCLC patients.
- Aids in optimizing NSCLC treatment strategies and clinical decision-making for dose modifications.
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