Related Experiment Video
Updated: Jun 18, 2025

Profiling Sensitivity to Targeted Therapies in EGFR-Mutant NSCLC Patient-Derived Organoids
Published on: November 22, 2021
Treatment Patterns and Resource Use After Osimertinib Discontinuation in Patients with EGFR + Metastatic NSCLC
Elizabeth Marrett1, Winghan Jacqueline Kwong2, Jinlin Song3
1Health Economic and Outcomes Research, Daiichi Sankyo, Inc., 211 Mount Airy Road, Basking Ridge, NJ, 07920, USA. elizabeth.marrett@daiichisankyo.com.
Introduction:
Current treatment guidelines for patients with epidermal growth factor receptor (EGFR)-mutated metastatic non-small cell lung cancer (mNSCLC) recommend EGFR tyrosine kinase inhibitors (TKIs) as the standard of care for first-line treatment, with third-generation osimertinib the preferred choice. However, most patients develop resistance to targeted therapy, and subsequent systemic chemotherapy is recommended. The aim of this study was to characterize the subsequent line of therapy (LOT) following osimertinib in patients with EGFR-mNSCLC.
Methods:
Medical and pharmacy claims of adults who initiated a subsequent LOT (index) after initial osimertinib discontinuation between November 2015 and September 2019 were analyzed retrospectively.
Results:
A total of 135 patients met the inclusion criteria. After metastatic diagnosis, 22.2% and 49.6% of patients were treated with osimertinib in the first and second line, respectively. After osimertinib discontinuation, most patients were treated with a platinum-based chemotherapy regimen (57%), of which 40.3% included immuno-oncology therapy. Reuse or continuation of EGFR TKIs was also common (24%). Overall, the median time to treatment discontinuation for the index LOT was 2.4 months. Proportions of patients with ≥ 1 inpatient or emergency department visit were 31.9% and 35.6%, respectively.
Conclusions:
The duration of the LOT following osimertinib was short and associated with tolerability issues underscoring a high unmet need for new therapies to address EGFR TKI resistance.
Insights
Subsequent therapies for EGFR-mutated non-small cell lung cancer after osimertinib are often short-lived. Most patients receive platinum-based chemotherapy, highlighting an unmet need for more effective treatments against EGFR tyrosine kinase inhibitor resistance.
Area of Science:
- Oncology
- Pharmacology
- Clinical Research
Background:
- Current guidelines recommend EGFR tyrosine kinase inhibitors (TKIs), particularly osimertinib, for first-line treatment of EGFR-mutated metastatic non-small cell lung cancer (mNSCLC).
- Acquired resistance to targeted therapies like osimertinib is common, necessitating subsequent treatment lines.
- Systemic chemotherapy is typically recommended after progression on targeted therapy.
Purpose of the Study:
- To characterize the subsequent line of therapy (LOT) following osimertinib discontinuation in patients with EGFR-mutated mNSCLC.
- To evaluate treatment patterns and duration of subsequent therapies.
- To identify unmet needs in managing EGFR TKI resistance.
Main Methods:
- Retrospective analysis of medical and pharmacy claims data.
- Inclusion of adult patients who initiated a subsequent LOT after discontinuing osimertinib between November 2015 and September 2019.
- Characterization of treatment regimens, duration, and healthcare utilization.
Main Results:
- 135 patients met the inclusion criteria.
- Most patients (57%) received platinum-based chemotherapy in the subsequent LOT, with 40.3% including immuno-oncology therapy.
- EGFR TKI reuse or continuation was observed in 24% of patients.
- The median time to treatment discontinuation for the subsequent LOT was short (2.4 months).
- Significant proportions of patients experienced inpatient (31.9%) or emergency department (35.6%) visits.
Conclusions:
- The subsequent line of therapy following osimertinib in EGFR-mNSCLC is often of short duration.
- Tolerability issues appear to be a significant factor contributing to treatment discontinuation.
- There is a high unmet need for novel therapeutic strategies to overcome EGFR TKI resistance.
More Related Videos
09:38Establishment and Characterization of Three Afatinib-resistant Lung Adenocarcinoma PC-9 Cell Lines Developed with Increasing Doses of Afatinib
Published on: June 26, 2019
09:38Establishing Dual Resistance to EGFR-TKI and MET-TKI in Lung Adenocarcinoma Cells In Vitro with a 2-step Dose-escalation Procedure
Published on: August 11, 2017
Related Concept Videos
Targeted Cancer Therapies
There are several types of targeted therapies against...
Cancer Therapies
However, cancer treatments can pose several challenges, as therapies used to kill cancer cells are generally also toxic to normal cells. Moreover, cancer cells mutate rapidly and can develop resistance to chemical agents or radiation therapy. Besides, all types of cancer cells may not respond to the same therapy. Some cancer cells respond to one...
Cancer Survival Analysis