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Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma

BACKGROUND: The aim of this research was to evaluate clinical and low-cost genetic determinants of treatment outcome in EGFR mutation positive advanced lung adenocarcinoma patients. MATERIAL AND METHODS: EGFR mutation testing and EGFR 181946C>T genotyping were performed in 101 advanced lung adeno...

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Autores principales: Jokic, Vera, Savic-Vujovic, Katarina, Spasic, Jelena, Bukumiric, Zoran, Marinkovic, Mladen, Radosavljevic, Davorin, Cavic, Milena
Formato: Online Artículo Texto
Lenguaje:English
Publicado: SAGE Publications 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358214/
https://www.ncbi.nlm.nih.gov/pubmed/35958274
http://dx.doi.org/10.1177/15593258221117354
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author Jokic, Vera
Savic-Vujovic, Katarina
Spasic, Jelena
Bukumiric, Zoran
Marinkovic, Mladen
Radosavljevic, Davorin
Cavic, Milena
author_facet Jokic, Vera
Savic-Vujovic, Katarina
Spasic, Jelena
Bukumiric, Zoran
Marinkovic, Mladen
Radosavljevic, Davorin
Cavic, Milena
author_sort Jokic, Vera
collection PubMed
description BACKGROUND: The aim of this research was to evaluate clinical and low-cost genetic determinants of treatment outcome in EGFR mutation positive advanced lung adenocarcinoma patients. MATERIAL AND METHODS: EGFR mutation testing and EGFR 181946C>T genotyping were performed in 101 advanced lung adenocarcinoma patients using qRT-PCR and PCR-RFLP, respectively. Progression-free survival was defined as the time from the start of TKI therapy to date of progression, and overall survival as the time from diagnosis to death from any cause. Pain level was evaluated using a Numerical Rating Scale and the Verbal Descriptor Scale. Statistical significance was considered for P < .05. RESULTS: Patients were treated with EGFR-TKIs for a period of 1–39months (median 9), with a median PFS of 12.0 months (10.4-13.6, CI 95%), and a median OS of 19.0 months (15.1-22.7, CI 95%). The presence of pain was significantly correlated with the existence of bone (P < .001) and adrenal glands metastases (P = .029). Genetic factors did not have a direct impact on pain management but had a significant effect on the response to TKIs leading to pain alleviation. CONCLUSIONS: EGFR mutation subtype and the EGFR 181946 C>T SNP had a significant effect on the response to TKI inducing an indirect anti-dolorous effect.
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spelling pubmed-93582142022-08-10 Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma Jokic, Vera Savic-Vujovic, Katarina Spasic, Jelena Bukumiric, Zoran Marinkovic, Mladen Radosavljevic, Davorin Cavic, Milena Dose Response Original Article BACKGROUND: The aim of this research was to evaluate clinical and low-cost genetic determinants of treatment outcome in EGFR mutation positive advanced lung adenocarcinoma patients. MATERIAL AND METHODS: EGFR mutation testing and EGFR 181946C>T genotyping were performed in 101 advanced lung adenocarcinoma patients using qRT-PCR and PCR-RFLP, respectively. Progression-free survival was defined as the time from the start of TKI therapy to date of progression, and overall survival as the time from diagnosis to death from any cause. Pain level was evaluated using a Numerical Rating Scale and the Verbal Descriptor Scale. Statistical significance was considered for P < .05. RESULTS: Patients were treated with EGFR-TKIs for a period of 1–39months (median 9), with a median PFS of 12.0 months (10.4-13.6, CI 95%), and a median OS of 19.0 months (15.1-22.7, CI 95%). The presence of pain was significantly correlated with the existence of bone (P < .001) and adrenal glands metastases (P = .029). Genetic factors did not have a direct impact on pain management but had a significant effect on the response to TKIs leading to pain alleviation. CONCLUSIONS: EGFR mutation subtype and the EGFR 181946 C>T SNP had a significant effect on the response to TKI inducing an indirect anti-dolorous effect. SAGE Publications 2022-08-04 /pmc/articles/PMC9358214/ /pubmed/35958274 http://dx.doi.org/10.1177/15593258221117354 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by-nc/4.0/This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage).
spellingShingle Original Article
Jokic, Vera
Savic-Vujovic, Katarina
Spasic, Jelena
Bukumiric, Zoran
Marinkovic, Mladen
Radosavljevic, Davorin
Cavic, Milena
Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma
title Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma
title_full Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma
title_fullStr Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma
title_full_unstemmed Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma
title_short Evaluation of Clinical and Genetic Determinants of Treatment OutCome In EGFR Mutation Positive Advanced Lung Adenocarcinoma
title_sort evaluation of clinical and genetic determinants of treatment outcome in egfr mutation positive advanced lung adenocarcinoma
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9358214/
https://www.ncbi.nlm.nih.gov/pubmed/35958274
http://dx.doi.org/10.1177/15593258221117354
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