Related Experiment Video
Updated: Apr 22, 2026

Author Spotlight: Advancements in Molecular Biomarker Testing for Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
Treatment Patterns Across Lines of Therapy for Advanced Non-Small Cell Lung Cancer in the United States
Do H Lee1, Yimeng Li2, Szu-Chun Yang2,3
1Cancer Outcomes, Cancer Outcomes, Public Policy, and Effectiveness Research (COPPER) Center, Yale School of Medicine, New Haven, Connecticut, USA.
Introduction:
Treatment strategies for advanced non-small cell lung cancer (aNSCLC) have evolved, but little is known about real-world approaches by biomarker groups across different lines of therapy (LOTs), particularly regarding discontinuation rates as a measure of effectiveness and tolerability.
Methods:
Using deidentified patient data from the Flatiron Health electronic health record-derived database, we constructed a retrospective cohort study of aNSCLC patients diagnosed between January 2016 and June 2020, with follow-up through August 2023. Patients had either anaplastic lymphoma kinase (ALK) rearrangements or epidermal growth factor receptor (EGFR) mutations or had programmed cell death-ligand 1 (PD-L1) biomarker results (PD-L1 < 1%, 1%-49%, or ≥ 50%). For each biomarker group, we summarized treatments received across up to the sixth LOT, calculating the overall discontinuation rate and the rate due to death.
Results:
There were 13,369 patients in our sample (427 patients with ALK rearrangements, 2283 with EGFR mutations, 3663 PD-L1 < 1%, 3281 PD-L1 1%-49%, and 3715 PD-L1 ≥ 50%). Treatment patterns varied across biomarker groups. The overall discontinuation rate after first-line therapy was 31.9% for ALK-rearrangement, 39.5% for EGFR-mutation, and ranged from 50.6% to 57.5% for the PD-L1 groups. The discontinuation rate due to death after first-line therapy was 8% (ALK-rearrangement), 14.8% (EGFR-mutation), and approximately 21% for the three PD-L1 groups. Patients with gene alterations had lower overall discontinuation rates across second through fifth LOTs than those without.
Conclusions:
Patients with driver alterations had lower overall discontinuation rates in subsequent therapy lines, highlighting the need for effective, tolerable treatments for those without driver alterations. Notably, a substantial proportion of patients with targetable driver alterations did not receive the corresponding TKI, underscoring real-world gaps in biomarker-directed treatment implementation.
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
04:04Endobronchial Ultrasound-guided Intratumoral Injection of Cisplatin for the Treatment of Isolated Mediastinal Recurrence of Lung Cancer
Published on: February 12, 2017
Related Concept Videos
Treatment Resistent Cancers
Targeted Cancer Therapies
There are several types of targeted therapies against...
Targeted Cancer Therapies
Treatment Resistant Cancers
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 Therapies