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获得性表皮生长因子酪氨酸激酶抑制剂耐药后的组织学转化。

Histological transformation after acquired resistance to epidermal growth factor tyrosine kinase inhibitors.

机构信息

Department of Medical Oncology, Tianjin Medical University General Hospital, No154 Anshan Road, Heping Dist, Tianjin, 300052, China.

出版信息

Int J Clin Oncol. 2018 Apr;23(2):235-242. doi: 10.1007/s10147-017-1211-1. Epub 2017 Nov 7.

DOI:10.1007/s10147-017-1211-1
PMID:29110101
Abstract

Non-small-cell lung cancer patients with sensitive epidermal growth factor receptor mutations generally respond well to tyrosine kinase inhibitors (TKIs). However, acquired resistance will eventually develop place after 8-16 months. Several mechanisms contribute to the resistance including T790M mutation, c-Met amplification, epithelial mesenchymal transformation and PIK3CA mutation; however, histological transformation is a rare mechanism. The patterns and mechanisms underlying histological transformation need to be explored. We searched PubMed, EMBASE and search engines Google Scholar, Medical Matrix for literature related to histological transformation. Case reports, cases series, and clinical and basic medical research articles were reviewed. Sixty-one articles were included in this review. Cases of transformation to small-cell lung cancer, squamous cell carcinoma, large-cell neuroendocrine carcinoma and sarcoma after TKI resistance have all been reported. As the clinical course differed dramatically between cases, a new treatment scheme needs to be recruited. The mechanisms underlying histological transformation have not been fully elucidated and probably relate to cancer stem cells, driver genetic alterations under selective pressure or the heterogeneity of the tumor. When TKI resistance develops, we recommend that patients undergo a second biopsy to determine the reason, guide the next treatment and predict the prognosis.

摘要

具有敏感表皮生长因子受体突变的非小细胞肺癌患者通常对酪氨酸激酶抑制剂 (TKI) 反应良好。然而,在 8-16 个月后,获得性耐药最终会发生。几种机制导致耐药,包括 T790M 突变、c-Met 扩增、上皮间质转化和 PIK3CA 突变;然而,组织学转化是一种罕见的机制。需要探索组织学转化的模式和机制。我们在 PubMed、EMBASE 和搜索引擎 Google Scholar、Medical Matrix 中搜索了与组织学转化相关的文献。综述了病例报告、病例系列和临床及基础医学研究文章。本综述共纳入 61 篇文章。报道了 TKI 耐药后转化为小细胞肺癌、鳞状细胞癌、大细胞神经内分泌癌和肉瘤的病例。由于病例之间的临床过程差异很大,需要招募新的治疗方案。组织学转化的机制尚未完全阐明,可能与癌症干细胞、选择性压力下的驱动基因突变或肿瘤的异质性有关。当 TKI 耐药发生时,我们建议患者进行第二次活检以确定原因,指导下一步治疗并预测预后。

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免疫检查点阻断治疗后肺腺癌患者发生组织学肉瘤样转化。
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