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Transformation of non-small cell lung cancer into small cell lung cancer in a patient with advanced lung cancer: a case report
Targeted therapy in patients with epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC) often fails because of drug resistance. Here, we report a 57-year-old male patient with stage IV small cell lung cancer (SCLC) transformation during targeted therapy. Chest computeriz...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371742/ https://www.ncbi.nlm.nih.gov/pubmed/34396834 http://dx.doi.org/10.1177/03000605211035005 |
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author | Yang, Zhengyuan Lin, Yingcheng Wang, Hongbiao |
author_facet | Yang, Zhengyuan Lin, Yingcheng Wang, Hongbiao |
author_sort | Yang, Zhengyuan |
collection | PubMed |
description | Targeted therapy in patients with epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC) often fails because of drug resistance. Here, we report a 57-year-old male patient with stage IV small cell lung cancer (SCLC) transformation during targeted therapy. Chest computerized tomography (CT), hematoxylin and eosin histological examination, immunohistochemistry, allele refractory mutation system‐based quantitative polymerase chain reaction analysis of EGFR point mutations, and next-generation sequencing were performed for diagnosis and therapeutic efficacy evaluation. A combination of chest CT, histological examination, and immunohistochemistry confirmed the initial NSCLC diagnosis. Next-generation sequencing detected only EGFR exon 19 deletion (ex19del) before treatment and later identified EGFR exon20p.T790M point mutation, EGFR amplification, myc proto-oncogene (MYC) amplification, retinoblastoma 1 (RB1) mutation, and tumor protein 53 (TP53) mutation. Histology and immunohistochemistry revealed transformation from NSCLC to SCLC during treatment, which eventually returned to NSCLC. Drug resistance to targeted therapy for patients with NSCLC frequently occurs because of EGFR exon20p.T790M point mutation, TP53 mutation, RB1 mutation, and MYC amplification. These mutations are also the major determining factors of NSCLC outcomes. Therefore, next-generation sequencing should be performed to confirm drug efficacy during targeted therapy for NSCLC. |
format | Online Article Text |
id | pubmed-8371742 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-83717422021-08-19 Transformation of non-small cell lung cancer into small cell lung cancer in a patient with advanced lung cancer: a case report Yang, Zhengyuan Lin, Yingcheng Wang, Hongbiao J Int Med Res Case Reports Targeted therapy in patients with epidermal growth factor receptor (EGFR)-mutated non-small cell lung cancer (NSCLC) often fails because of drug resistance. Here, we report a 57-year-old male patient with stage IV small cell lung cancer (SCLC) transformation during targeted therapy. Chest computerized tomography (CT), hematoxylin and eosin histological examination, immunohistochemistry, allele refractory mutation system‐based quantitative polymerase chain reaction analysis of EGFR point mutations, and next-generation sequencing were performed for diagnosis and therapeutic efficacy evaluation. A combination of chest CT, histological examination, and immunohistochemistry confirmed the initial NSCLC diagnosis. Next-generation sequencing detected only EGFR exon 19 deletion (ex19del) before treatment and later identified EGFR exon20p.T790M point mutation, EGFR amplification, myc proto-oncogene (MYC) amplification, retinoblastoma 1 (RB1) mutation, and tumor protein 53 (TP53) mutation. Histology and immunohistochemistry revealed transformation from NSCLC to SCLC during treatment, which eventually returned to NSCLC. Drug resistance to targeted therapy for patients with NSCLC frequently occurs because of EGFR exon20p.T790M point mutation, TP53 mutation, RB1 mutation, and MYC amplification. These mutations are also the major determining factors of NSCLC outcomes. Therefore, next-generation sequencing should be performed to confirm drug efficacy during targeted therapy for NSCLC. SAGE Publications 2021-08-16 /pmc/articles/PMC8371742/ /pubmed/34396834 http://dx.doi.org/10.1177/03000605211035005 Text en © The Author(s) 2021 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 | Case Reports Yang, Zhengyuan Lin, Yingcheng Wang, Hongbiao Transformation of non-small cell lung cancer into small cell lung cancer in a patient with advanced lung cancer: a case report |
title | Transformation of non-small cell lung cancer into small cell lung
cancer in a patient with advanced lung cancer: a case report |
title_full | Transformation of non-small cell lung cancer into small cell lung
cancer in a patient with advanced lung cancer: a case report |
title_fullStr | Transformation of non-small cell lung cancer into small cell lung
cancer in a patient with advanced lung cancer: a case report |
title_full_unstemmed | Transformation of non-small cell lung cancer into small cell lung
cancer in a patient with advanced lung cancer: a case report |
title_short | Transformation of non-small cell lung cancer into small cell lung
cancer in a patient with advanced lung cancer: a case report |
title_sort | transformation of non-small cell lung cancer into small cell lung
cancer in a patient with advanced lung cancer: a case report |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8371742/ https://www.ncbi.nlm.nih.gov/pubmed/34396834 http://dx.doi.org/10.1177/03000605211035005 |
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