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非小细胞肺癌中ROS1基因重排及其临床意义

Chromosomal rearrangements involving the ROS1 receptor tyrosine kinase gene have recently been described in multiple malignancies, including non-small cell lung cancer (NSCLC). ROS1 rearrangement defines a new molecular subset of NSCLC with the prevalence of ROS1 rearrangements around 1%-2%. ROS1-po...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000642/
https://www.ncbi.nlm.nih.gov/pubmed/24345493
http://dx.doi.org/10.3779/j.issn.1009-3419.2013.12.09
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description Chromosomal rearrangements involving the ROS1 receptor tyrosine kinase gene have recently been described in multiple malignancies, including non-small cell lung cancer (NSCLC). ROS1 rearrangement defines a new molecular subset of NSCLC with the prevalence of ROS1 rearrangements around 1%-2%. ROS1-positive NSCLCs arise in young never-smokers with adenocarcinoma that are similar to those observed in patients with ALK-rearranged NSCLC. Crizotinib demonstrates in vitro activity and early clinical trial shows marked antitumor activity in ROS1-rearranged patients. The overall response rate is around 56% and the disease control rate at 8 weeks is about 76%. Further understanding the ROS1 fusions in the pathogenesis of NSCLC, methods to detect ROS1 rearrangements, and targeting ROS1-rearranged NSCLC patients with specific kinase inhibitors would lead to an era of personalized medicine.
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spelling pubmed-60006422018-07-06 非小细胞肺癌中ROS1基因重排及其临床意义 Zhongguo Fei Ai Za Zhi 综述 Chromosomal rearrangements involving the ROS1 receptor tyrosine kinase gene have recently been described in multiple malignancies, including non-small cell lung cancer (NSCLC). ROS1 rearrangement defines a new molecular subset of NSCLC with the prevalence of ROS1 rearrangements around 1%-2%. ROS1-positive NSCLCs arise in young never-smokers with adenocarcinoma that are similar to those observed in patients with ALK-rearranged NSCLC. Crizotinib demonstrates in vitro activity and early clinical trial shows marked antitumor activity in ROS1-rearranged patients. The overall response rate is around 56% and the disease control rate at 8 weeks is about 76%. Further understanding the ROS1 fusions in the pathogenesis of NSCLC, methods to detect ROS1 rearrangements, and targeting ROS1-rearranged NSCLC patients with specific kinase inhibitors would lead to an era of personalized medicine. 中国肺癌杂志编辑部 2013-12-20 /pmc/articles/PMC6000642/ /pubmed/24345493 http://dx.doi.org/10.3779/j.issn.1009-3419.2013.12.09 Text en 版权所有©《中国肺癌杂志》编辑部2013 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 综述
非小细胞肺癌中ROS1基因重排及其临床意义
title 非小细胞肺癌中ROS1基因重排及其临床意义
title_full 非小细胞肺癌中ROS1基因重排及其临床意义
title_fullStr 非小细胞肺癌中ROS1基因重排及其临床意义
title_full_unstemmed 非小细胞肺癌中ROS1基因重排及其临床意义
title_short 非小细胞肺癌中ROS1基因重排及其临床意义
title_sort 非小细胞肺癌中ros1基因重排及其临床意义
topic 综述
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6000642/
https://www.ncbi.nlm.nih.gov/pubmed/24345493
http://dx.doi.org/10.3779/j.issn.1009-3419.2013.12.09
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