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Pitfalls in diagnosis with the use of circulating tumor‐derived epidermal growth factor receptor mutations in lung cancer harboring pretreatment T790M
The circulating tumor DNA (ctDNA) assay has recently been approved for the selection of EGFR‐tyrosine kinase inhibitors as first‐line treatment in lung cancer. However, it remains to be determined whether this assay can detect all complex EGFR mutations within a single tumor. We report a case of an...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754312/ https://www.ncbi.nlm.nih.gov/pubmed/29063709 http://dx.doi.org/10.1111/1759-7714.12538 |
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author | Ogawara, Daiki Soda, Hiroshi Suyama, Takayuki Yoshida, Masataka Harada, Tatsuhiko Fukuda, Yuichi Mukae, Hiroshi |
author_facet | Ogawara, Daiki Soda, Hiroshi Suyama, Takayuki Yoshida, Masataka Harada, Tatsuhiko Fukuda, Yuichi Mukae, Hiroshi |
author_sort | Ogawara, Daiki |
collection | PubMed |
description | The circulating tumor DNA (ctDNA) assay has recently been approved for the selection of EGFR‐tyrosine kinase inhibitors as first‐line treatment in lung cancer. However, it remains to be determined whether this assay can detect all complex EGFR mutations within a single tumor. We report a case of an elderly woman with stage IV lung adenocarcinoma, in which EGFR mutation assays detected L858R and pretreatment T790M from a tissue biopsy. In contrast, the circulating tumor DNA assay detected L858R, but not pretreatment T790M in the plasma, regardless of the fact that similar amounts of each mutation were present in the biopsy specimen. Treatment with afatinib was not effective, but subsequent treatment with osimertinib remarkably regressed the tumor. Our findings indicate that physicians should accurately evaluate EGFR‐tyrosine kinase inhibitor‐insensitive mutations using tissue samples in the first‐line setting, even when L858R and exon 19 deletions are detected in the plasma. |
format | Online Article Text |
id | pubmed-5754312 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-57543122018-01-09 Pitfalls in diagnosis with the use of circulating tumor‐derived epidermal growth factor receptor mutations in lung cancer harboring pretreatment T790M Ogawara, Daiki Soda, Hiroshi Suyama, Takayuki Yoshida, Masataka Harada, Tatsuhiko Fukuda, Yuichi Mukae, Hiroshi Thorac Cancer Case Reports The circulating tumor DNA (ctDNA) assay has recently been approved for the selection of EGFR‐tyrosine kinase inhibitors as first‐line treatment in lung cancer. However, it remains to be determined whether this assay can detect all complex EGFR mutations within a single tumor. We report a case of an elderly woman with stage IV lung adenocarcinoma, in which EGFR mutation assays detected L858R and pretreatment T790M from a tissue biopsy. In contrast, the circulating tumor DNA assay detected L858R, but not pretreatment T790M in the plasma, regardless of the fact that similar amounts of each mutation were present in the biopsy specimen. Treatment with afatinib was not effective, but subsequent treatment with osimertinib remarkably regressed the tumor. Our findings indicate that physicians should accurately evaluate EGFR‐tyrosine kinase inhibitor‐insensitive mutations using tissue samples in the first‐line setting, even when L858R and exon 19 deletions are detected in the plasma. John Wiley & Sons Australia, Ltd 2017-10-24 2018-01 /pmc/articles/PMC5754312/ /pubmed/29063709 http://dx.doi.org/10.1111/1759-7714.12538 Text en © 2017 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial (http://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes. |
spellingShingle | Case Reports Ogawara, Daiki Soda, Hiroshi Suyama, Takayuki Yoshida, Masataka Harada, Tatsuhiko Fukuda, Yuichi Mukae, Hiroshi Pitfalls in diagnosis with the use of circulating tumor‐derived epidermal growth factor receptor mutations in lung cancer harboring pretreatment T790M |
title | Pitfalls in diagnosis with the use of circulating tumor‐derived epidermal growth factor receptor mutations in lung cancer harboring pretreatment T790M |
title_full | Pitfalls in diagnosis with the use of circulating tumor‐derived epidermal growth factor receptor mutations in lung cancer harboring pretreatment T790M |
title_fullStr | Pitfalls in diagnosis with the use of circulating tumor‐derived epidermal growth factor receptor mutations in lung cancer harboring pretreatment T790M |
title_full_unstemmed | Pitfalls in diagnosis with the use of circulating tumor‐derived epidermal growth factor receptor mutations in lung cancer harboring pretreatment T790M |
title_short | Pitfalls in diagnosis with the use of circulating tumor‐derived epidermal growth factor receptor mutations in lung cancer harboring pretreatment T790M |
title_sort | pitfalls in diagnosis with the use of circulating tumor‐derived epidermal growth factor receptor mutations in lung cancer harboring pretreatment t790m |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5754312/ https://www.ncbi.nlm.nih.gov/pubmed/29063709 http://dx.doi.org/10.1111/1759-7714.12538 |
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