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Successful treatment of refractory brain metastases from ALK‐positive lung cancer with lorlatinib

A 44‐year‐old woman with ALK‐positive advanced adenocarcinoma of the lung was treated with crizotinib, and the lung lesions disappeared. The patient was treated with alectinib and chemotherapy, but brain metastases worsened; therefore, we performed an ALK resistance gene mutation test using plasma s...

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Detalles Bibliográficos
Autores principales: Nakagawa, Yoshiko, Shimizu, Tetsuo, Hiranuma, Hisato, Gon, Yasuhiro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley & Sons Australia, Ltd 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058295/
https://www.ncbi.nlm.nih.gov/pubmed/35373538
http://dx.doi.org/10.1111/1759-7714.14406
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author Nakagawa, Yoshiko
Shimizu, Tetsuo
Hiranuma, Hisato
Gon, Yasuhiro
author_facet Nakagawa, Yoshiko
Shimizu, Tetsuo
Hiranuma, Hisato
Gon, Yasuhiro
author_sort Nakagawa, Yoshiko
collection PubMed
description A 44‐year‐old woman with ALK‐positive advanced adenocarcinoma of the lung was treated with crizotinib, and the lung lesions disappeared. The patient was treated with alectinib and chemotherapy, but brain metastases worsened; therefore, we performed an ALK resistance gene mutation test using plasma samples. Since no ALK resistance gene mutations were detected, we speculated that ALK inhibitors failed to achieve therapeutic effects due to poor transport to the central nervous system. Therefore, we switched to lorlatinib, and found a reduction in brain metastases. In ALK‐positive advanced lung cancer, plasma‐based resistance gene testing may be useful for treatment decisions.
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spelling pubmed-90582952022-05-03 Successful treatment of refractory brain metastases from ALK‐positive lung cancer with lorlatinib Nakagawa, Yoshiko Shimizu, Tetsuo Hiranuma, Hisato Gon, Yasuhiro Thorac Cancer Case Reports A 44‐year‐old woman with ALK‐positive advanced adenocarcinoma of the lung was treated with crizotinib, and the lung lesions disappeared. The patient was treated with alectinib and chemotherapy, but brain metastases worsened; therefore, we performed an ALK resistance gene mutation test using plasma samples. Since no ALK resistance gene mutations were detected, we speculated that ALK inhibitors failed to achieve therapeutic effects due to poor transport to the central nervous system. Therefore, we switched to lorlatinib, and found a reduction in brain metastases. In ALK‐positive advanced lung cancer, plasma‐based resistance gene testing may be useful for treatment decisions. John Wiley & Sons Australia, Ltd 2022-04-04 2022-05 /pmc/articles/PMC9058295/ /pubmed/35373538 http://dx.doi.org/10.1111/1759-7714.14406 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-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Case Reports
Nakagawa, Yoshiko
Shimizu, Tetsuo
Hiranuma, Hisato
Gon, Yasuhiro
Successful treatment of refractory brain metastases from ALK‐positive lung cancer with lorlatinib
title Successful treatment of refractory brain metastases from ALK‐positive lung cancer with lorlatinib
title_full Successful treatment of refractory brain metastases from ALK‐positive lung cancer with lorlatinib
title_fullStr Successful treatment of refractory brain metastases from ALK‐positive lung cancer with lorlatinib
title_full_unstemmed Successful treatment of refractory brain metastases from ALK‐positive lung cancer with lorlatinib
title_short Successful treatment of refractory brain metastases from ALK‐positive lung cancer with lorlatinib
title_sort successful treatment of refractory brain metastases from alk‐positive lung cancer with lorlatinib
topic Case Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9058295/
https://www.ncbi.nlm.nih.gov/pubmed/35373538
http://dx.doi.org/10.1111/1759-7714.14406
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