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Comprehensive analysis of aneuploidy status and its effect on the efficacy of EGFR-TKIs in lung cancer

BACKGROUND: Lung cancer has the highest mortality rate among cancers worldwide, and most patients are diagnosed with non-small-cell lung cancer (NSCLC), and evaluating the clinical efficacy of molecularly targeted cancer therapy remains a major challenge. METHODS: This paper retrospectively investig...

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Autores principales: Wei, Bing, Zhao, Chengzhi, Yang, Ke, Yan, Chi, Chang, Yuxi, Gao, Huijie, Guo, Yongjun, Ma, Jie
Formato: Online Artículo Texto
Lenguaje:English
Publicado: AME Publishing Company 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987823/
https://www.ncbi.nlm.nih.gov/pubmed/35399233
http://dx.doi.org/10.21037/jtd-22-73
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author Wei, Bing
Zhao, Chengzhi
Yang, Ke
Yan, Chi
Chang, Yuxi
Gao, Huijie
Guo, Yongjun
Ma, Jie
author_facet Wei, Bing
Zhao, Chengzhi
Yang, Ke
Yan, Chi
Chang, Yuxi
Gao, Huijie
Guo, Yongjun
Ma, Jie
author_sort Wei, Bing
collection PubMed
description BACKGROUND: Lung cancer has the highest mortality rate among cancers worldwide, and most patients are diagnosed with non-small-cell lung cancer (NSCLC), and evaluating the clinical efficacy of molecularly targeted cancer therapy remains a major challenge. METHODS: This paper retrospectively investigated the outcome information of 291 lung cancer patients detected by next-generation sequencing (NGS) analysis and fluorescence in situ hybridization (FISH), including 63 patients with lung cancer who were followed up. We analyzed epidermal growth factor receptor (EGFR) mutation abundance and aneuploidy status to evaluate clinical efficacy. RESULTS: The progress free survival (PFS) of patients diagnosed as euploidy was actually higher than that of patients diagnosed with aneuploidy, and was related to both the objective response rate (ORR) and disease control rate (DCR). Patients with an epidermal growth factor receptor (EGFR) mutation abundance ≥28.86% had slightly higher ORR and similar DCR. Two-way analysis of variance was used to assess the effects of EGFR mutation abundance and tumor aneuploidy status on patients’ PFS. The results indicated a strong correlation between aneuploidy status and clinical efficacy, with euploid patients having a higher ORR and DCR. CONCLUSIONS: Aneuploidy status could effectively evaluate the clinical efficacy of patients with lung cancer. However, EGFR mutations abundance could not predict the extent of benefit from tyrosine kinase inhibitors (EGFR-TKI) treatment.
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spelling pubmed-89878232022-04-08 Comprehensive analysis of aneuploidy status and its effect on the efficacy of EGFR-TKIs in lung cancer Wei, Bing Zhao, Chengzhi Yang, Ke Yan, Chi Chang, Yuxi Gao, Huijie Guo, Yongjun Ma, Jie J Thorac Dis Original Article BACKGROUND: Lung cancer has the highest mortality rate among cancers worldwide, and most patients are diagnosed with non-small-cell lung cancer (NSCLC), and evaluating the clinical efficacy of molecularly targeted cancer therapy remains a major challenge. METHODS: This paper retrospectively investigated the outcome information of 291 lung cancer patients detected by next-generation sequencing (NGS) analysis and fluorescence in situ hybridization (FISH), including 63 patients with lung cancer who were followed up. We analyzed epidermal growth factor receptor (EGFR) mutation abundance and aneuploidy status to evaluate clinical efficacy. RESULTS: The progress free survival (PFS) of patients diagnosed as euploidy was actually higher than that of patients diagnosed with aneuploidy, and was related to both the objective response rate (ORR) and disease control rate (DCR). Patients with an epidermal growth factor receptor (EGFR) mutation abundance ≥28.86% had slightly higher ORR and similar DCR. Two-way analysis of variance was used to assess the effects of EGFR mutation abundance and tumor aneuploidy status on patients’ PFS. The results indicated a strong correlation between aneuploidy status and clinical efficacy, with euploid patients having a higher ORR and DCR. CONCLUSIONS: Aneuploidy status could effectively evaluate the clinical efficacy of patients with lung cancer. However, EGFR mutations abundance could not predict the extent of benefit from tyrosine kinase inhibitors (EGFR-TKI) treatment. AME Publishing Company 2022-03 /pmc/articles/PMC8987823/ /pubmed/35399233 http://dx.doi.org/10.21037/jtd-22-73 Text en 2022 Journal of Thoracic Disease. All rights reserved. https://creativecommons.org/licenses/by-nc-nd/4.0/Open Access Statement: This is an Open Access article distributed in accordance with the Creative Commons Attribution-NonCommercial-NoDerivs 4.0 International License (CC BY-NC-ND 4.0), which permits the non-commercial replication and distribution of the article with the strict proviso that no changes or edits are made and the original work is properly cited (including links to both the formal publication through the relevant DOI and the license). See: https://creativecommons.org/licenses/by-nc-nd/4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) .
spellingShingle Original Article
Wei, Bing
Zhao, Chengzhi
Yang, Ke
Yan, Chi
Chang, Yuxi
Gao, Huijie
Guo, Yongjun
Ma, Jie
Comprehensive analysis of aneuploidy status and its effect on the efficacy of EGFR-TKIs in lung cancer
title Comprehensive analysis of aneuploidy status and its effect on the efficacy of EGFR-TKIs in lung cancer
title_full Comprehensive analysis of aneuploidy status and its effect on the efficacy of EGFR-TKIs in lung cancer
title_fullStr Comprehensive analysis of aneuploidy status and its effect on the efficacy of EGFR-TKIs in lung cancer
title_full_unstemmed Comprehensive analysis of aneuploidy status and its effect on the efficacy of EGFR-TKIs in lung cancer
title_short Comprehensive analysis of aneuploidy status and its effect on the efficacy of EGFR-TKIs in lung cancer
title_sort comprehensive analysis of aneuploidy status and its effect on the efficacy of egfr-tkis in lung cancer
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8987823/
https://www.ncbi.nlm.nih.gov/pubmed/35399233
http://dx.doi.org/10.21037/jtd-22-73
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