Andrea Kohánka, László Báthory-Fülöp, Eszter Tanács-Bencze, Helga Engi, Krisztina Bogos, Judit Moldvay, Zsolt Székely Pápai, Zsuzsanna Szalai, János Szőke, Erika Tóth
{"title":"[肺腺癌分子病理学,表皮生长因子受体 T790M 抗性突变研究]。","authors":"Andrea Kohánka, László Báthory-Fülöp, Eszter Tanács-Bencze, Helga Engi, Krisztina Bogos, Judit Moldvay, Zsolt Székely Pápai, Zsuzsanna Szalai, János Szőke, Erika Tóth","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Aim: </strong>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.</p><p><strong>Methods: </strong>380, predominantly blood samples from 222 patients were tested during the present period using Super- ARMS EGFR Mutation Detection Kit (AmoyDx).</p><p><strong>Results: </strong>EGFR mutations were identified in 57% of all samples in the primary tumours, with a 38.3% frequency of T790M mutation.</p><p><strong>Conclusions: </strong>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.</p>","PeriodicalId":94127,"journal":{"name":"Magyar onkologia","volume":"68 4","pages":"334"},"PeriodicalIF":0.0000,"publicationDate":"2024-12-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"[Molecular pathology of lung adenocarcinomas, EGFR T790M resistance mutation study].\",\"authors\":\"Andrea Kohánka, László Báthory-Fülöp, Eszter Tanács-Bencze, Helga Engi, Krisztina Bogos, Judit Moldvay, Zsolt Székely Pápai, Zsuzsanna Szalai, János Szőke, Erika Tóth\",\"doi\":\"\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Aim: </strong>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.</p><p><strong>Methods: </strong>380, predominantly blood samples from 222 patients were tested during the present period using Super- ARMS EGFR Mutation Detection Kit (AmoyDx).</p><p><strong>Results: </strong>EGFR mutations were identified in 57% of all samples in the primary tumours, with a 38.3% frequency of T790M mutation.</p><p><strong>Conclusions: </strong>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.</p>\",\"PeriodicalId\":94127,\"journal\":{\"name\":\"Magyar onkologia\",\"volume\":\"68 4\",\"pages\":\"334\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-12-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Magyar onkologia\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/11/20 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Magyar onkologia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/20 0:00:00","PubModel":"Epub","JCR":"","JCRName":"","Score":null,"Total":0}
[Molecular pathology of lung adenocarcinomas, EGFR T790M resistance mutation study].
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.