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循环肿瘤细胞在ALK阳性非小细胞肺癌中的临床应用

Clinical Utility of Circulating Tumor Cells in ALK-Positive Non-Small-Cell Lung Cancer.

作者信息

Faugeroux Vincent, Pailler Emma, Auger Nathalie, Taylor Melissa, Farace Françoise

机构信息

INSERM U981 "Identification of Molecular Predictors and New Targets for Cancer Treatment," Institut Gustave Roussy, University of Paris-Sud , Paris , France ; Translational Research Laboratory, Institut Gustave Roussy , Paris , France.

Department of Biopathology, Institut Gustave Roussy , Paris , France.

出版信息

Front Oncol. 2014 Nov 5;4:281. doi: 10.3389/fonc.2014.00281. eCollection 2014.

Abstract

The advent of rationally targeted therapies such as small-molecule tyrosine kinase inhibitors (TKIs) has considerably transformed the therapeutic management of a subset of patients with non-small-cell lung cancer (NSCLC) harboring defined molecular abnormalities. When such genetic molecular alterations are detected the use of specific TKI has demonstrated better results (overall response rate, progression free survival) compared to systemic therapy. However, the detection of such molecular abnormalities is complicated by the difficulty in obtaining sufficient tumor material, in terms of quantity and quality, from a biopsy. Here, we described how circulating tumor cells (CTCs) can have a clinical utility in anaplastic lymphoma kinase (ALK) positive NSCLC patients to diagnose ALK-EML4 gene rearrangement and to guide therapeutic management of these patients. The ability to detect genetic abnormalities such ALK rearrangement in CTCs shows that these cells could offer new perspectives both for the diagnosis and the monitoring of ALK-positive patients eligible for treatment with ALK inhibitors.

摘要

诸如小分子酪氨酸激酶抑制剂(TKIs)等合理靶向疗法的出现,极大地改变了一部分患有特定分子异常的非小细胞肺癌(NSCLC)患者的治疗管理方式。当检测到此类基因分子改变时,与全身治疗相比,使用特定的TKI已显示出更好的效果(总体缓解率、无进展生存期)。然而,由于难以从活检中获取足够数量和质量的肿瘤材料,此类分子异常的检测变得复杂。在此,我们描述了循环肿瘤细胞(CTC)在间变性淋巴瘤激酶(ALK)阳性NSCLC患者中如何具有临床应用价值,以诊断ALK-EML4基因重排并指导这些患者的治疗管理。在CTC中检测到诸如ALK重排等基因异常的能力表明,这些细胞可为诊断和监测适合用ALK抑制剂治疗的ALK阳性患者提供新的视角。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/31ea/4220657/1978003b53bd/fonc-04-00281-g001.jpg

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