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RET融合型非小细胞肺癌的研究进展

In the past 20 years, with the development of molecular biology, the treatment of non-small cell lung cancer (NSCLC) has been developing. Targeted therapy has improved the survival period of patients with positive mutation of tumor driver gene. More and more targets have been found gradually. Drugs...

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Detalles Bibliográficos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 中国肺癌杂志编辑部 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387645/
https://www.ncbi.nlm.nih.gov/pubmed/34120433
http://dx.doi.org/10.3779/j.issn.1009-3419.2021.102.22
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description In the past 20 years, with the development of molecular biology, the treatment of non-small cell lung cancer (NSCLC) has been developing. Targeted therapy has improved the survival period of patients with positive mutation of tumor driver gene. More and more targets have been found gradually. Drugs targeting different driving genes have brought the treatment of NSCLC into a promising target era. Among the many driving genes of NSCLC, the fusion of transfection proto oncogene (RET) is the addition of the epidermal growth factor receptor (EGFR), analytic lymphama kinase (ALK) and c-ros oncogene 1-receptor tyrosine kinase (ROS1) are emerging targets. Targeted drugs for RET gene fusion have been constantly updated. Recently, new high selective RET inhibitors blu-667 and loxo-292 have made important breakthroughs. This paper will review the review of the fusion mutation of RET gene in NSCLC, the detection methods, clinicopathological characteristics, targeted treatment and the research progress after drug resistance.
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spelling pubmed-83876452021-09-14 RET融合型非小细胞肺癌的研究进展 Zhongguo Fei Ai Za Zhi 综述 In the past 20 years, with the development of molecular biology, the treatment of non-small cell lung cancer (NSCLC) has been developing. Targeted therapy has improved the survival period of patients with positive mutation of tumor driver gene. More and more targets have been found gradually. Drugs targeting different driving genes have brought the treatment of NSCLC into a promising target era. Among the many driving genes of NSCLC, the fusion of transfection proto oncogene (RET) is the addition of the epidermal growth factor receptor (EGFR), analytic lymphama kinase (ALK) and c-ros oncogene 1-receptor tyrosine kinase (ROS1) are emerging targets. Targeted drugs for RET gene fusion have been constantly updated. Recently, new high selective RET inhibitors blu-667 and loxo-292 have made important breakthroughs. This paper will review the review of the fusion mutation of RET gene in NSCLC, the detection methods, clinicopathological characteristics, targeted treatment and the research progress after drug resistance. 中国肺癌杂志编辑部 2021-08-20 /pmc/articles/PMC8387645/ /pubmed/34120433 http://dx.doi.org/10.3779/j.issn.1009-3419.2021.102.22 Text en 版权所有©《中国肺癌杂志》编辑部2021 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
RET融合型非小细胞肺癌的研究进展
title RET融合型非小细胞肺癌的研究进展
title_full RET融合型非小细胞肺癌的研究进展
title_fullStr RET融合型非小细胞肺癌的研究进展
title_full_unstemmed RET融合型非小细胞肺癌的研究进展
title_short RET融合型非小细胞肺癌的研究进展
title_sort ret融合型非小细胞肺癌的研究进展
topic 综述
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8387645/
https://www.ncbi.nlm.nih.gov/pubmed/34120433
http://dx.doi.org/10.3779/j.issn.1009-3419.2021.102.22
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