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Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring EGFR L858R and L747V mutations
Epidermal growth factor receptor (EGFR)‐tyrosine kinase inhibitors are standard therapeutic agents for non‐small cell lung cancer (NSCLC) patients with major EGFR mutations such as exon 19 deletions and a L858R mutation, whereas treatment strategies for cases with uncommon EGFR mutations remain to b...
Autores principales: | , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons Australia, Ltd
2022
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663673/ https://www.ncbi.nlm.nih.gov/pubmed/36193787 http://dx.doi.org/10.1111/1759-7714.14678 |
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author | Kanbe, Mio Sunaga, Noriaki Hara, Kenichiro Sawada, Hiiru Wakamatsu, Ikuo Hara, Kentaro Muto, Sohei Sawada, Yuri Masubuchi, Hiroaki Sato, Mari Miura, Yosuke Tsurumaki, Hiroaki Yatomi, Masakiyo Sakurai, Reiko Koga, Yasuhiko Ohtaki, Yoichi Nagashima, Toshiteru Okano, Naoko Kubo, Nobuteru Maeno, Toshitaka Hisada, Takeshi |
author_facet | Kanbe, Mio Sunaga, Noriaki Hara, Kenichiro Sawada, Hiiru Wakamatsu, Ikuo Hara, Kentaro Muto, Sohei Sawada, Yuri Masubuchi, Hiroaki Sato, Mari Miura, Yosuke Tsurumaki, Hiroaki Yatomi, Masakiyo Sakurai, Reiko Koga, Yasuhiko Ohtaki, Yoichi Nagashima, Toshiteru Okano, Naoko Kubo, Nobuteru Maeno, Toshitaka Hisada, Takeshi |
author_sort | Kanbe, Mio |
collection | PubMed |
description | Epidermal growth factor receptor (EGFR)‐tyrosine kinase inhibitors are standard therapeutic agents for non‐small cell lung cancer (NSCLC) patients with major EGFR mutations such as exon 19 deletions and a L858R mutation, whereas treatment strategies for cases with uncommon EGFR mutations remain to be fully established. Here, we report a long‐term (≥20 years from initial diagnosis) NSCLC survivor carrying EGFR L858R and L747V mutations. The patient received gefitinib monotherapy, systemic chemotherapy/chemoimmunotherapy, and local consolidative therapies for oligometastatic lesions, and responded to afatinib rechallenge with a progression‐free survival of 12 months. The current case suggests that afatinib is effective in NSCLC patients with EGFR L858R and L747V mutations and that a therapeutic approach combining appropriately timed systemic therapies with local consolidative therapies for oligometastatic lesions improves long‐term survival. |
format | Online Article Text |
id | pubmed-9663673 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley & Sons Australia, Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-96636732022-11-16 Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring EGFR L858R and L747V mutations Kanbe, Mio Sunaga, Noriaki Hara, Kenichiro Sawada, Hiiru Wakamatsu, Ikuo Hara, Kentaro Muto, Sohei Sawada, Yuri Masubuchi, Hiroaki Sato, Mari Miura, Yosuke Tsurumaki, Hiroaki Yatomi, Masakiyo Sakurai, Reiko Koga, Yasuhiko Ohtaki, Yoichi Nagashima, Toshiteru Okano, Naoko Kubo, Nobuteru Maeno, Toshitaka Hisada, Takeshi Thorac Cancer Case Reports Epidermal growth factor receptor (EGFR)‐tyrosine kinase inhibitors are standard therapeutic agents for non‐small cell lung cancer (NSCLC) patients with major EGFR mutations such as exon 19 deletions and a L858R mutation, whereas treatment strategies for cases with uncommon EGFR mutations remain to be fully established. Here, we report a long‐term (≥20 years from initial diagnosis) NSCLC survivor carrying EGFR L858R and L747V mutations. The patient received gefitinib monotherapy, systemic chemotherapy/chemoimmunotherapy, and local consolidative therapies for oligometastatic lesions, and responded to afatinib rechallenge with a progression‐free survival of 12 months. The current case suggests that afatinib is effective in NSCLC patients with EGFR L858R and L747V mutations and that a therapeutic approach combining appropriately timed systemic therapies with local consolidative therapies for oligometastatic lesions improves long‐term survival. John Wiley & Sons Australia, Ltd 2022-10-04 2022-11 /pmc/articles/PMC9663673/ /pubmed/36193787 http://dx.doi.org/10.1111/1759-7714.14678 Text en © 2022 The Authors. Thoracic Cancer published by China Lung Oncology Group and John Wiley & Sons Australia, Ltd. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://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 Kanbe, Mio Sunaga, Noriaki Hara, Kenichiro Sawada, Hiiru Wakamatsu, Ikuo Hara, Kentaro Muto, Sohei Sawada, Yuri Masubuchi, Hiroaki Sato, Mari Miura, Yosuke Tsurumaki, Hiroaki Yatomi, Masakiyo Sakurai, Reiko Koga, Yasuhiko Ohtaki, Yoichi Nagashima, Toshiteru Okano, Naoko Kubo, Nobuteru Maeno, Toshitaka Hisada, Takeshi Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring EGFR L858R and L747V mutations |
title | Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring
EGFR L858R and L747V mutations |
title_full | Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring
EGFR L858R and L747V mutations |
title_fullStr | Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring
EGFR L858R and L747V mutations |
title_full_unstemmed | Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring
EGFR L858R and L747V mutations |
title_short | Durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring
EGFR L858R and L747V mutations |
title_sort | durable response to afatinib rechallenge in a long‐term survivor of non‐small cell lung cancer harboring
egfr l858r and l747v mutations |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9663673/ https://www.ncbi.nlm.nih.gov/pubmed/36193787 http://dx.doi.org/10.1111/1759-7714.14678 |
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