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具有ROS1重排的肺腺癌对克唑替尼的疾病进展模式和分子耐药机制。

Disease progression patterns and molecular resistance mechanisms to crizotinib of lung adenocarcinoma harboring ROS1 rearrangements.

作者信息

Zhang Yongchang, Huang Zhe, Zeng Liang, Zhang Xiangyu, Li Yizhi, Xu Qinqin, Yang Haiyan, Lizaso Analyn, Xu Chunwei, Liu Jun, Wang Wenxian, Song Zhengbo, Ou Sai-Hong Ignatius, Yang Nong

机构信息

Department of Medical Oncology, Lung Cancer and Gastrointestinal Unit, Hunan Cancer Hospital/The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University, 410013, Changsha, China.

Graduate Collaborative Training Base of Hunan Cancer Hospital, Hengyang Medical School, University of South China, Hengyang, 421001, Hunan, China.

出版信息

NPJ Precis Oncol. 2022 Mar 31;6(1):20. doi: 10.1038/s41698-022-00264-w.

DOI:10.1038/s41698-022-00264-w
PMID:35361870
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8971474/
Abstract

This retrospective study investigated the association between the pattern of disease progression and molecular mechanism of acquired resistance in a large cohort of 49 patients with ROS1-rearranged advanced non-small-cell lung cancer treated with first-line crizotinib. We found that treatment-emergent ROS1 point mutations were the major molecular mechanism of crizotinib resistance, particularly for patients who developed extracranial-only disease progression. Our findings highlight the importance of rebiopsy and gene testing for subsequent-line therapeutic management.

摘要

这项回顾性研究调查了49例接受一线克唑替尼治疗的ROS1重排晚期非小细胞肺癌患者的疾病进展模式与获得性耐药分子机制之间的关联。我们发现,治疗中出现的ROS1点突变是克唑替尼耐药的主要分子机制,尤其是对于仅发生颅外疾病进展的患者。我们的研究结果突出了再次活检和基因检测对后续治疗管理的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8380/8971474/c6521685344c/41698_2022_264_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8380/8971474/1ca0ae29e0c0/41698_2022_264_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8380/8971474/c6521685344c/41698_2022_264_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8380/8971474/1ca0ae29e0c0/41698_2022_264_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8380/8971474/c6521685344c/41698_2022_264_Fig2_HTML.jpg

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本文引用的文献

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BMC Med. 2021 Sep 13;19(1):206. doi: 10.1186/s12916-021-02082-6.
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Spectrum of Mechanisms of Resistance to Crizotinib and Lorlatinib in Fusion-Positive Lung Cancer.克唑替尼和劳拉替尼耐药机制的研究进展:融合阳性肺癌。
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靶向治疗癌症受体酪氨酸激酶的治疗进展。
Signal Transduct Target Ther. 2024 Aug 14;9(1):201. doi: 10.1038/s41392-024-01899-w.
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Rutin attenuates ensartinib-induced hepatotoxicity by non-transcriptional regulation of TXNIP.芦丁通过非转录调控 TXNIP 减轻恩沙替尼所致肝毒性。
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Lorlatinib and capmatinib in a ROS1-rearranged NSCLC with MET-driven resistance: tumor response and evolution.劳拉替尼和卡马替尼用于治疗具有MET驱动耐药性的ROS1重排非小细胞肺癌:肿瘤反应与演变
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