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Personalized drug testing in a patient with non-small-cell lung cancer using cultured cancer cells from pleural effusion
OBJECTIVE: Patients with non-small-cell lung cancer (NSCLC) and primary or acquired resistance do not respond to targeted drugs. We explored whether cancer cells can be cultured from liquid biopsies from patients with primary resistance to tyrosine kinase inhibitors (TKIs). We aimed to predict patie...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509736/ https://www.ncbi.nlm.nih.gov/pubmed/32954884 http://dx.doi.org/10.1177/0300060520955058 |
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author | Wu, Ming Hong, Guodai Chen, Yu Ye, Lina Zhang, Kang Cai, Kaihong Yang, Huadong Long, Xiang Gao, Wenbin Li, Hui |
author_facet | Wu, Ming Hong, Guodai Chen, Yu Ye, Lina Zhang, Kang Cai, Kaihong Yang, Huadong Long, Xiang Gao, Wenbin Li, Hui |
author_sort | Wu, Ming |
collection | PubMed |
description | OBJECTIVE: Patients with non-small-cell lung cancer (NSCLC) and primary or acquired resistance do not respond to targeted drugs. We explored whether cancer cells can be cultured from liquid biopsies from patients with primary resistance to tyrosine kinase inhibitors (TKIs). We aimed to predict patients’ responses to drugs according to in vitro drug testing results. METHODS: Cancer cell cultures were established from the pleural effusion of a patient with TKI-resistant NSCLC using a conditional reprogramming technique. Phenotypic drug sensitivity tests were performed using the Cell Counting Kit-8 assay. We tested individual drugs and compared the synergistic and inhibitory effects of drug combinations. RESULTS: The results of our in vitro sensitivity test using the combination of cisplatin and pemetrexed were correlated with the patient’s response. CONCLUSION: This represents the first successful report of predictive testing for combination therapy in patients with epidermal growth factor receptor-mutant NSCLC and primary TKI resistance. This strategy should be applicable to both chemotherapies and targeted therapies, and it will significantly improve the clinical treatment and management of patients with NSCLC and primary or acquired resistance to targeted therapies, as well as patients lacking targetable mutations. |
format | Online Article Text |
id | pubmed-7509736 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-75097362020-10-01 Personalized drug testing in a patient with non-small-cell lung cancer using cultured cancer cells from pleural effusion Wu, Ming Hong, Guodai Chen, Yu Ye, Lina Zhang, Kang Cai, Kaihong Yang, Huadong Long, Xiang Gao, Wenbin Li, Hui J Int Med Res Prospective Clinical Research Report OBJECTIVE: Patients with non-small-cell lung cancer (NSCLC) and primary or acquired resistance do not respond to targeted drugs. We explored whether cancer cells can be cultured from liquid biopsies from patients with primary resistance to tyrosine kinase inhibitors (TKIs). We aimed to predict patients’ responses to drugs according to in vitro drug testing results. METHODS: Cancer cell cultures were established from the pleural effusion of a patient with TKI-resistant NSCLC using a conditional reprogramming technique. Phenotypic drug sensitivity tests were performed using the Cell Counting Kit-8 assay. We tested individual drugs and compared the synergistic and inhibitory effects of drug combinations. RESULTS: The results of our in vitro sensitivity test using the combination of cisplatin and pemetrexed were correlated with the patient’s response. CONCLUSION: This represents the first successful report of predictive testing for combination therapy in patients with epidermal growth factor receptor-mutant NSCLC and primary TKI resistance. This strategy should be applicable to both chemotherapies and targeted therapies, and it will significantly improve the clinical treatment and management of patients with NSCLC and primary or acquired resistance to targeted therapies, as well as patients lacking targetable mutations. SAGE Publications 2020-09-21 /pmc/articles/PMC7509736/ /pubmed/32954884 http://dx.doi.org/10.1177/0300060520955058 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ Creative Commons Non Commercial CC BY-NC: 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 | Prospective Clinical Research Report Wu, Ming Hong, Guodai Chen, Yu Ye, Lina Zhang, Kang Cai, Kaihong Yang, Huadong Long, Xiang Gao, Wenbin Li, Hui Personalized drug testing in a patient with non-small-cell lung cancer using cultured cancer cells from pleural effusion |
title | Personalized drug testing in a patient with non-small-cell lung cancer using cultured cancer cells from pleural effusion |
title_full | Personalized drug testing in a patient with non-small-cell lung cancer using cultured cancer cells from pleural effusion |
title_fullStr | Personalized drug testing in a patient with non-small-cell lung cancer using cultured cancer cells from pleural effusion |
title_full_unstemmed | Personalized drug testing in a patient with non-small-cell lung cancer using cultured cancer cells from pleural effusion |
title_short | Personalized drug testing in a patient with non-small-cell lung cancer using cultured cancer cells from pleural effusion |
title_sort | personalized drug testing in a patient with non-small-cell lung cancer using cultured cancer cells from pleural effusion |
topic | Prospective Clinical Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7509736/ https://www.ncbi.nlm.nih.gov/pubmed/32954884 http://dx.doi.org/10.1177/0300060520955058 |
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