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ALK 阳性非小细胞肺癌中谱系可塑性的生物学特性及影响:一篇综述

Biology and impact of lineage plasticity in ALK-positive NSCLC: a narrative review.

作者信息

Meador Catherine B, Piotrowska Zofia

机构信息

Division of Hematology/Oncology, Department of Medicine, Massachusetts General Hospital/Harvard Medical School, Boston, MA, USA.

出版信息

Transl Lung Cancer Res. 2023 Apr 28;12(4):837-856. doi: 10.21037/tlcr-22-867. Epub 2023 Mar 22.

Abstract

BACKGROUND AND OBJECTIVE

Lineage transformation is a known mechanism of acquired resistance to targeted therapies in non-small cell lung cancer (NSCLC). Transformation to small cell and squamous carcinoma and epithelial-to-mesenchymal transition (EMT) have all been identified as recurrent but rare events in ALK-positive NSCLC. However, centralized data informing our understanding of the biology and clinical implications of lineage transformation in ALK-positive NSCLC are lacking.

METHODS

We performed a narrative review by searching the PubMed and clinicaltrials.gov databases for articles published in English from August, 2007 until October, 2022 and reviewing the bibliographies of key references to identify important literature related to lineage transformation in ALK-positive NSCLC.

KEY CONTENT AND FINDINGS

In this review, we aimed to synthesize the published literature describing the incidence, mechanism(s), and clinical outcomes of lineage transformation in ALK-positive NSCLC. Lineage transformation as a mechanism of resistance to ALK TKIs in ALK-positive NSCLC is reported at a frequency of <5%. Available data across molecular subtypes of NSCLC suggest that the process of lineage transformation is likely to be driven by transcriptional reprogramming rather than acquired genomic mutations. Retrospective cohorts including tissue-based translational studies together with clinical outcomes make up the highest level of evidence that exists to inform treatment approach for patients with transfomed ALK-positive NSCLC.

CONCLUSIONS

The clinicopathologic features of transformed ALK-positive NSCLC as well as the biologic mechanisms underling lineage transformation remain incompletely understood. Prospective data are needed to develop improved diagnostic and treatment algorithms for patients with ALK-positive NSCLC that undergo lineage transformation.

摘要

背景与目的

谱系转化是已知的非小细胞肺癌(NSCLC)获得性靶向治疗耐药机制。向小细胞癌和鳞状细胞癌的转化以及上皮-间质转化(EMT)均已被确定为ALK阳性NSCLC中反复出现但罕见的事件。然而,目前缺乏集中数据来帮助我们理解ALK阳性NSCLC谱系转化的生物学特性和临床意义。

方法

我们通过检索PubMed和clinicaltrials.gov数据库,查找2007年8月至2022年10月期间发表的英文文章,并查阅关键参考文献的书目,以识别与ALK阳性NSCLC谱系转化相关的重要文献,进行了一项叙述性综述。

关键内容与发现

在本综述中,我们旨在综合已发表的文献,描述ALK阳性NSCLC谱系转化的发生率、机制及临床结局。ALK阳性NSCLC中,谱系转化作为对ALK酪氨酸激酶抑制剂(TKI)耐药的一种机制,报告频率<5%。NSCLC各分子亚型的现有数据表明,谱系转化过程可能由转录重编程驱动,而非获得性基因组突变。包括基于组织的转化研究及临床结局的回顾性队列构成了为转化型ALK阳性NSCLC患者治疗方案提供依据的现有最高级别证据。

结论

转化型ALK阳性NSCLC的临床病理特征以及谱系转化的生物学机制仍未完全明确。需要前瞻性数据来为发生谱系转化的ALK阳性NSCLC患者开发改进的诊断和治疗算法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/eed1/10183401/c3030eaf5812/tlcr-12-04-837-f1.jpg

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