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Updated: May 5, 2026

Next Generation Sequencing for the Detection of Actionable Mutations in Solid and Liquid Tumors
Published on: September 20, 2016
[Molecular pathology of lung adenocarcinomas, EGFR T790M resistance mutation study]
Andrea Kohánka1, László Báthory-Fülöp1, Eszter Tanács-Bencze1
1Sebészeti és Molekuláris Patológiai Osztály, Országos Onkológiai Intézet, Budapest, Hungary. dr.toth.erika@oncol.hu.
Aim:
In our institute, we have been testing EGFR T790M resistance mutations since 2019, which is the most common resistance mutation that develops during first-line, second- line EGFR TKI treatment of EGFR mutant lung adenocarcinomas. The importance of this study is that the identification of this mutation will allow the use of an effective third-generation TKI. In this article, we report on studies from January 2022 to August 2024, compared with our results from the 2019-2021 period.
Methods:
380, predominantly blood samples from 222 patients were tested during the present period using Super- ARMS EGFR Mutation Detection Kit (AmoyDx).
Results:
EGFR mutations were identified in 57% of all samples in the primary tumours, with a 38.3% frequency of T790M mutation.
Conclusions:
Our results were similar to the previous period. The number of rebiopsies was essentially unchanged compared to the 2019-2021 period, which may be the main reason why we were able to identify the mutation in a lower percentage compared to the T790M hit rate described in the literature.
Insights
Testing for the EGFR T790M resistance mutation in lung cancer patients is crucial for effective treatment. Our study found a 38.3% T790M mutation frequency, similar to previous findings.
Area of Science:
- Oncology
- Molecular Diagnostics
- Genetics
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