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ALK抑制剂在治疗NSCLC脑转移中的疗效及安全性研究进展

Lung cancer is one of the most lethal malignancies in the world, with non-small cell lung cancer (NSCLC) accounting for approximately 80%-85% of all pathological types. Approximately 30%-55% of NSCLC patients develop brain metastases. It has been reported that 5%-6% of patients with brain metastases...

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Autores principales: Yuchen, CHEN, Han, HAN, Jinpan, WEI, Qianyu, DU, Xiyong, WANG
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial board of Chinese Journal of Lung Cancer 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273149/
https://www.ncbi.nlm.nih.gov/pubmed/37316450
http://dx.doi.org/10.3779/j.issn.1009-3419.2023.101.10
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author Yuchen, CHEN
Han, HAN
Jinpan, WEI
Qianyu, DU
Xiyong, WANG
author_facet Yuchen, CHEN
Han, HAN
Jinpan, WEI
Qianyu, DU
Xiyong, WANG
author_sort Yuchen, CHEN
collection PubMed
description Lung cancer is one of the most lethal malignancies in the world, with non-small cell lung cancer (NSCLC) accounting for approximately 80%-85% of all pathological types. Approximately 30%-55% of NSCLC patients develop brain metastases. It has been reported that 5%-6% of patients with brain metastases harbor anaplastic lymphoma kinase (ALK) fusion. ALK-positive NSCLC patients have shown significant therapeutic benefits after treatment with ALK inhibitors. Over the past decade, ALK inhibitors have rapidly evolved and now exist in three generations: first-generation drugs such as Crizotinib; second-generation drugs including Alectinib, Brigatinib, Ceritinib, and Ensartinib; and third-generation drugs like Lorlatinib. These drugs have exhibited varying efficacy in treating brain metastases in ALK-positive NSCLC patients. However, the numerous options available for ALK inhibition present a challenge for clinical decision-making. Therefore, this review aims to provide clinical guidance by summarizing the efficacy and safety of ALK inhibitors in treating NSCLC brain metastases.
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spelling pubmed-102731492023-06-17 ALK抑制剂在治疗NSCLC脑转移中的疗效及安全性研究进展 Yuchen, CHEN Han, HAN Jinpan, WEI Qianyu, DU Xiyong, WANG Zhongguo Fei Ai Za Zhi Review Lung cancer is one of the most lethal malignancies in the world, with non-small cell lung cancer (NSCLC) accounting for approximately 80%-85% of all pathological types. Approximately 30%-55% of NSCLC patients develop brain metastases. It has been reported that 5%-6% of patients with brain metastases harbor anaplastic lymphoma kinase (ALK) fusion. ALK-positive NSCLC patients have shown significant therapeutic benefits after treatment with ALK inhibitors. Over the past decade, ALK inhibitors have rapidly evolved and now exist in three generations: first-generation drugs such as Crizotinib; second-generation drugs including Alectinib, Brigatinib, Ceritinib, and Ensartinib; and third-generation drugs like Lorlatinib. These drugs have exhibited varying efficacy in treating brain metastases in ALK-positive NSCLC patients. However, the numerous options available for ALK inhibition present a challenge for clinical decision-making. Therefore, this review aims to provide clinical guidance by summarizing the efficacy and safety of ALK inhibitors in treating NSCLC brain metastases. Editorial board of Chinese Journal of Lung Cancer 2023-05-20 /pmc/articles/PMC10273149/ /pubmed/37316450 http://dx.doi.org/10.3779/j.issn.1009-3419.2023.101.10 Text en Copyright © 2023《中国肺癌杂志》编辑部 https://creativecommons.org/licenses/by/3.0/This is an open access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 3.0) License. See: https://creativecommons.org/licenses/by/3.0/.
spellingShingle Review
Yuchen, CHEN
Han, HAN
Jinpan, WEI
Qianyu, DU
Xiyong, WANG
ALK抑制剂在治疗NSCLC脑转移中的疗效及安全性研究进展
title ALK抑制剂在治疗NSCLC脑转移中的疗效及安全性研究进展
title_full ALK抑制剂在治疗NSCLC脑转移中的疗效及安全性研究进展
title_fullStr ALK抑制剂在治疗NSCLC脑转移中的疗效及安全性研究进展
title_full_unstemmed ALK抑制剂在治疗NSCLC脑转移中的疗效及安全性研究进展
title_short ALK抑制剂在治疗NSCLC脑转移中的疗效及安全性研究进展
title_sort alk抑制剂在治疗nsclc脑转移中的疗效及安全性研究进展
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10273149/
https://www.ncbi.nlm.nih.gov/pubmed/37316450
http://dx.doi.org/10.3779/j.issn.1009-3419.2023.101.10
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