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Clinical Characteristics and Molecular Patterns of RET-Rearranged Lung Cancer in Chinese Patients
RET rearrangement has been proven as an oncogenic driver in patients with lung cancer. However, the prevalence, clinical characteristics, molecular features, and therapeutic options in RET-rearranged patients remain unclear, especially in Chinese lung cancer patients. We retrospectively collected 6,...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cognizant Communication Corporation
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848427/ https://www.ncbi.nlm.nih.gov/pubmed/30131091 http://dx.doi.org/10.3727/096504018X15344979253618 |
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author | Zhang, Kai Chen, Huajun Wang, Ye Yang, Lin Zhou, Chengzhi Yin, Weiqiang Wang, Guangsuo Mao, Xinru Xiang, Jianxing Li, Bing Zhang, Tengfei Fei, Shihong |
author_facet | Zhang, Kai Chen, Huajun Wang, Ye Yang, Lin Zhou, Chengzhi Yin, Weiqiang Wang, Guangsuo Mao, Xinru Xiang, Jianxing Li, Bing Zhang, Tengfei Fei, Shihong |
author_sort | Zhang, Kai |
collection | PubMed |
description | RET rearrangement has been proven as an oncogenic driver in patients with lung cancer. However, the prevalence, clinical characteristics, molecular features, and therapeutic options in RET-rearranged patients remain unclear, especially in Chinese lung cancer patients. We retrospectively collected 6,125 Chinese lung cancer patients who have been profiled using next-generation sequencing (NGS). The clinical demographics and molecular features of RET rearrangement-positive patients were analyzed. RET rearrangements were identified in 84 patients with a proportion of 1.4% in our cohort. The median age at diagnosis was 58 years, and it mainly occurred in females with adenocarcinoma histology. KIF5B-RET was the most frequent fusion type and accounted for 53.8% (57/106) of all RET fusions identified, with K15-R12 as the most frequent variant (71.9%). Among 47 RET (+) patients profiled with larger panels, 72.3% (34/47) harbored concurrent alterations. TP53 ranked as the most common concurrent alteration, and concomitant EGFR oncogenic alterations were identified in seven patients. Moreover, an adenocarcinoma patient harboring concurrent RET fusion and EGFR L858R responded to combinatorial treatment of cabozantinib and osimertinib, with a progression-free survival of 5 months. Our study improved knowledge of clinical characteristics and molecular features of RET-rearranged lung cancers in China. It might be helpful to guide clinicians for more effective personalized diagnostic and therapeutic approaches. |
format | Online Article Text |
id | pubmed-7848427 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Cognizant Communication Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-78484272021-02-16 Clinical Characteristics and Molecular Patterns of RET-Rearranged Lung Cancer in Chinese Patients Zhang, Kai Chen, Huajun Wang, Ye Yang, Lin Zhou, Chengzhi Yin, Weiqiang Wang, Guangsuo Mao, Xinru Xiang, Jianxing Li, Bing Zhang, Tengfei Fei, Shihong Oncol Res Article RET rearrangement has been proven as an oncogenic driver in patients with lung cancer. However, the prevalence, clinical characteristics, molecular features, and therapeutic options in RET-rearranged patients remain unclear, especially in Chinese lung cancer patients. We retrospectively collected 6,125 Chinese lung cancer patients who have been profiled using next-generation sequencing (NGS). The clinical demographics and molecular features of RET rearrangement-positive patients were analyzed. RET rearrangements were identified in 84 patients with a proportion of 1.4% in our cohort. The median age at diagnosis was 58 years, and it mainly occurred in females with adenocarcinoma histology. KIF5B-RET was the most frequent fusion type and accounted for 53.8% (57/106) of all RET fusions identified, with K15-R12 as the most frequent variant (71.9%). Among 47 RET (+) patients profiled with larger panels, 72.3% (34/47) harbored concurrent alterations. TP53 ranked as the most common concurrent alteration, and concomitant EGFR oncogenic alterations were identified in seven patients. Moreover, an adenocarcinoma patient harboring concurrent RET fusion and EGFR L858R responded to combinatorial treatment of cabozantinib and osimertinib, with a progression-free survival of 5 months. Our study improved knowledge of clinical characteristics and molecular features of RET-rearranged lung cancers in China. It might be helpful to guide clinicians for more effective personalized diagnostic and therapeutic approaches. Cognizant Communication Corporation 2019-05-07 /pmc/articles/PMC7848427/ /pubmed/30131091 http://dx.doi.org/10.3727/096504018X15344979253618 Text en Copyright © 2019 Cognizant, LLC. http://creativecommons.org/licenses/by-nc-nd/4.0/ This article is licensed under a Creative Commons Attribution-NonCommercial NoDerivatives 4.0 International License. |
spellingShingle | Article Zhang, Kai Chen, Huajun Wang, Ye Yang, Lin Zhou, Chengzhi Yin, Weiqiang Wang, Guangsuo Mao, Xinru Xiang, Jianxing Li, Bing Zhang, Tengfei Fei, Shihong Clinical Characteristics and Molecular Patterns of RET-Rearranged Lung Cancer in Chinese Patients |
title | Clinical Characteristics and Molecular Patterns of RET-Rearranged Lung Cancer in Chinese Patients |
title_full | Clinical Characteristics and Molecular Patterns of RET-Rearranged Lung Cancer in Chinese Patients |
title_fullStr | Clinical Characteristics and Molecular Patterns of RET-Rearranged Lung Cancer in Chinese Patients |
title_full_unstemmed | Clinical Characteristics and Molecular Patterns of RET-Rearranged Lung Cancer in Chinese Patients |
title_short | Clinical Characteristics and Molecular Patterns of RET-Rearranged Lung Cancer in Chinese Patients |
title_sort | clinical characteristics and molecular patterns of ret-rearranged lung cancer in chinese patients |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7848427/ https://www.ncbi.nlm.nih.gov/pubmed/30131091 http://dx.doi.org/10.3727/096504018X15344979253618 |
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