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Oncogenic Gene Fusion Detection Using Anchored Multiplex Polymerase Chain Reaction Followed by Next Generation Sequencing
Published on: July 5, 2019
Presence of On-Target Resistant Mutation in Pre-Treatment Samples of ALK Fusion Gene Positive Lung Cancer Patients
Weiting Li1, Fenneke Zwierenga2, Katarina D Andini3
1Department of Pathology and Medical Biology, University of Groningen, University Medical Centre Groningen, 9713 GZ Groningen, The Netherlands.
Abstract:
A subset of ALK+ non-small cell lung cancer (NSCLC) patients relapse on ALK inhibitor (ALKi) treatment due to on-target resistance mutations affecting the tyrosine kinase domain.
Objective:
In this study, we investigated the presence of minor resistant clones in pre-treatment tissue samples and assessed their predictive value for subsequent resistance mechanisms.
Methods:
Using the highly sensitive digital droplet (dd)PCR technique, we analyzed 40 tissue samples obtained from 17 patients who had developed on-target resistance mutations after receiving ALKi between 2013 and 2022. We focused on 10 on-target ALKi resistant mutations identified in our patient cohort.
Results:
Fifteen ALKi resistance mutations were detected in 13 samples from 11/17 patients. Among these, four mutations were observed as resistance mutations in follow-up biopsies taken after first or subsequent lines of ALKi. Comparison of the test results from two subsequent biopsies, before and directly after therapy, revealed presence of the resistance mutation identified upon relapse in the pre-treatment sample of three cases that were all taken from the same tumor location. In six cases taken from different tumor locations, the resistant mutations were not found in the pre-treatment sample.
Conclusions:
By using the highly sensitive ddPCR approach, we detected minor clones with on-target resistant mutations in both treatment-naive and relapse biopsies from ALK-positive NSCLC patients. The predictive value of these mutations as the potential resistance-causing mechanism was limited to relapses occurring at the same tumor location as the pre-treatment sample.
Insights
Minor resistant clones with on-target mutations in ALK-positive NSCLC patients were detected using ddPCR. Their predictive value for resistance was limited to relapses at the same tumor location as pre-treatment samples.
Area of Science:
- Oncology
- Molecular Biology
- Genetics
Background:
- A subset of ALK-positive non-small cell lung cancer (NSCLC) patients develop resistance to ALK inhibitors (ALKi) due to on-target mutations.
- Understanding the mechanisms of resistance is crucial for improving patient outcomes.
Purpose of the Study:
- To investigate the presence of minor resistant clones in pre-treatment tissue samples of ALK+ NSCLC patients.
- To assess the predictive value of these minor clones for subsequent resistance mechanisms to ALKi treatment.
Main Methods:
- Utilized highly sensitive digital droplet PCR (ddPCR) technique.
- Analyzed 40 tissue samples from 17 ALK+ NSCLC patients treated with ALKi between 2013 and 2022.
- Focused on 10 known on-target ALKi resistance mutations.
Main Results:
- Detected 15 ALKi resistance mutations in 13 samples from 11 patients.
- Four mutations found in follow-up biopsies were also present in pre-treatment samples from the same tumor location in 3 cases.
- Resistant mutations were not found in pre-treatment samples from different tumor locations in 6 cases.
Conclusions:
- Highly sensitive ddPCR can detect minor clones with on-target resistant mutations in ALK+ NSCLC patients.
- The predictive value of these pre-treatment mutations for resistance is limited to relapses occurring at the same tumor site.
- Further research may explore spatial heterogeneity of resistance mechanisms in NSCLC.
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