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癌基因依赖型非小细胞肺癌的形态-分子转化。

Morphologic-Molecular Transformation of Oncogene Addicted Non-Small Cell Lung Cancer.

机构信息

Department of Cardiac, Thoracic, Vascular Sciences, and Public Health, University of Padova, 35128 Padova, Italy.

Department of Pathology, Aristotle University of Thessaloniki, 541 24 Thessaloniki, Greece.

出版信息

Int J Mol Sci. 2022 Apr 9;23(8):4164. doi: 10.3390/ijms23084164.

Abstract

Patients with non-small cell lung cancer, especially adenocarcinomas, harbour at least one oncogenic driver mutation that can potentially be a target for therapy. Treatments of these oncogene-addicted tumours, such as the use of tyrosine kinase inhibitors (TKIs) of mutated epidermal growth factor receptor, have dramatically improved the outcome of patients. However, some patients may acquire resistance to treatment early on after starting a targeted therapy. Transformations to other histotypes-small cell lung carcinoma, large cell neuroendocrine carcinoma, squamous cell carcinoma, and sarcomatoid carcinoma-have been increasingly recognised as important mechanisms of resistance and are increasingly becoming a topic of interest for all specialists involved in the diagnosis, management, and care of these patients. This article, after examining the most used TKI agents and their main biological activities, discusses histological and molecular transformations with an up-to-date review of all previous cases published in the field. Liquid biopsy and future research directions are also briefly discussed to offer the reader a complete and up-to-date overview of the topic.

摘要

非小细胞肺癌患者,尤其是腺癌,至少存在一种可能成为治疗靶点的致癌驱动突变。针对这些对致癌基因上瘾的肿瘤的治疗方法,如使用表皮生长因子受体突变的酪氨酸激酶抑制剂(TKI),已显著改善了患者的预后。然而,一些患者在开始靶向治疗后可能会很快产生耐药性。向其他组织类型的转化——小细胞肺癌、大细胞神经内分泌癌、鳞状细胞癌和肉瘤样癌——已被越来越多地认为是耐药的重要机制,并且越来越成为参与这些患者的诊断、管理和护理的所有专家关注的话题。本文在研究了最常用的 TKI 药物及其主要生物学活性后,讨论了组织学和分子转化,并对该领域发表的所有先前病例进行了最新回顾。还简要讨论了液体活检和未来的研究方向,为读者提供了该主题的全面最新概述。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9474/9031930/8a0ac7b19753/ijms-23-04164-g001.jpg

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