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Successful salvage surgery followed by second ALK–TKI after alectinib failure in a patient with ALK-positive NSCLC
BACKGROUND: Anaplastic lymphoma kinase (ALK)–tyrosine kinase inhibitors (TKIs) have been approved for the therapy of locally advanced non-small cell lung cancer (NSCLC) caused by ALK rearrangement. However, its treatment after failure of initial ALK–TKI therapy remains controversial. CASE PRESENTATI...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976869/ https://www.ncbi.nlm.nih.gov/pubmed/35366157 http://dx.doi.org/10.1186/s40792-022-01408-7 |
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author | Hashimoto, Hiroshi Komori, Kazuyuki Kameda, Koji Taguchi, Shinichi Ozeki, Yuichi |
author_facet | Hashimoto, Hiroshi Komori, Kazuyuki Kameda, Koji Taguchi, Shinichi Ozeki, Yuichi |
author_sort | Hashimoto, Hiroshi |
collection | PubMed |
description | BACKGROUND: Anaplastic lymphoma kinase (ALK)–tyrosine kinase inhibitors (TKIs) have been approved for the therapy of locally advanced non-small cell lung cancer (NSCLC) caused by ALK rearrangement. However, its treatment after failure of initial ALK–TKI therapy remains controversial. CASE PRESENTATION: A 47-year-old woman with a hemosputum was diagnosed with adenocarcinoma of the left lung (cT2bN3M0, stage IIIB). Gene mutation analysis indicated positive ALK translocation. Alectinib was selected as the first-line treatment. Although the treatment effect was determined as a partial response, the main tumor regrew. Alectinib was discontinued, and salvage surgery was performed without causing morbidity. The pathological diagnosis was pleomorphic carcinoma without lymph node metastasis (yp-T2bN0). After surgery, lorlatinib was administered as the second-line treatment for 8 months until the patient could not tolerate continuation. Computed tomography scan revealed no lung cancer recurrence 14 months after discontinuation. CONCLUSIONS: Our experience with this case suggests that salvage surgery after alectinib treatment followed by lorlatinib therapy may be effective for initially unresectable ALK-positive NSCLC. |
format | Online Article Text |
id | pubmed-8976869 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-89768692022-04-20 Successful salvage surgery followed by second ALK–TKI after alectinib failure in a patient with ALK-positive NSCLC Hashimoto, Hiroshi Komori, Kazuyuki Kameda, Koji Taguchi, Shinichi Ozeki, Yuichi Surg Case Rep Case Report BACKGROUND: Anaplastic lymphoma kinase (ALK)–tyrosine kinase inhibitors (TKIs) have been approved for the therapy of locally advanced non-small cell lung cancer (NSCLC) caused by ALK rearrangement. However, its treatment after failure of initial ALK–TKI therapy remains controversial. CASE PRESENTATION: A 47-year-old woman with a hemosputum was diagnosed with adenocarcinoma of the left lung (cT2bN3M0, stage IIIB). Gene mutation analysis indicated positive ALK translocation. Alectinib was selected as the first-line treatment. Although the treatment effect was determined as a partial response, the main tumor regrew. Alectinib was discontinued, and salvage surgery was performed without causing morbidity. The pathological diagnosis was pleomorphic carcinoma without lymph node metastasis (yp-T2bN0). After surgery, lorlatinib was administered as the second-line treatment for 8 months until the patient could not tolerate continuation. Computed tomography scan revealed no lung cancer recurrence 14 months after discontinuation. CONCLUSIONS: Our experience with this case suggests that salvage surgery after alectinib treatment followed by lorlatinib therapy may be effective for initially unresectable ALK-positive NSCLC. Springer Berlin Heidelberg 2022-04-02 /pmc/articles/PMC8976869/ /pubmed/35366157 http://dx.doi.org/10.1186/s40792-022-01408-7 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Case Report Hashimoto, Hiroshi Komori, Kazuyuki Kameda, Koji Taguchi, Shinichi Ozeki, Yuichi Successful salvage surgery followed by second ALK–TKI after alectinib failure in a patient with ALK-positive NSCLC |
title | Successful salvage surgery followed by second ALK–TKI after alectinib failure in a patient with ALK-positive NSCLC |
title_full | Successful salvage surgery followed by second ALK–TKI after alectinib failure in a patient with ALK-positive NSCLC |
title_fullStr | Successful salvage surgery followed by second ALK–TKI after alectinib failure in a patient with ALK-positive NSCLC |
title_full_unstemmed | Successful salvage surgery followed by second ALK–TKI after alectinib failure in a patient with ALK-positive NSCLC |
title_short | Successful salvage surgery followed by second ALK–TKI after alectinib failure in a patient with ALK-positive NSCLC |
title_sort | successful salvage surgery followed by second alk–tki after alectinib failure in a patient with alk-positive nsclc |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8976869/ https://www.ncbi.nlm.nih.gov/pubmed/35366157 http://dx.doi.org/10.1186/s40792-022-01408-7 |
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