寡转移性 NSCLC 的预后和预测生物标志物:新见解和临床应用

IF 3 Q2 ONCOLOGY
Mandy Jongbloed MD , Martina Bortolot MD , Leonard Wee PhD , Jarno W.J. Huijs MD , Murillo Bellezo PhD , Rianne D.W. Vaes PhD , Frank Aboubakar Nana MD, PhD , Koen J. Hartemink MD, PhD , Dirk K.M. De Ruysscher MD, PhD , Lizza E.L. Hendriks MD, PhD
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引用次数: 0

摘要

这篇综述讨论了寡转移 NSCLC 预测和预后生物标志物的现有数据,并讨论了在其他阶段和广泛转移性疾病中发现的生物标志物能否推断出寡转移疾病 (OMD) 的情况。目前正在开展研究,探索肿瘤组织、循环细胞、肿瘤微环境的生物属性以及成像结果作为寡转移 NSCLC 生物标志物的预后和预测价值。需要有助于定义真正的寡转移性NSCLC并预测预后的生物标志物来选择接受寡转移治疗的患者,并避免对无法从局部治疗中获益的患者进行徒劳无益的治疗。然而,这些生物标志物仍处于早期开发阶段,缺乏临床试验的前瞻性验证。此外,由于缺乏对 OMD 的明确定义,不同类型的 OMD 混杂在一起,治疗策略也不尽相同,这就造成了研究人群的异质性。基于组织、循环和成像的多种特征有望在 NSCLC 中发挥预后和预测作用,但数据仍然有限,而且由于纳入了异质性患者群体,可能会出现偏差。要评估这些生物标志物的预后和预测作用,需要更大规模的同质前瞻性系列研究。由于获取组织可能比较困难,而且是侵入性的,因此最有希望进一步评估的工具是液体活检和基于成像的生物标志物,因为它们也可用于纵向随访。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Prognostic and Predictive Biomarkers of Oligometastatic NSCLC: New Insights and Clinical Applications
This review discusses the current data on predictive and prognostic biomarkers in oligometastatic NSCLC and discusses whether biomarkers identified in other stages and widespread metastatic disease can be extrapolated to the oligometastatic disease (OMD) setting. Research is underway to explore the prognostic and predictive value of biological attributes of tumor tissue, circulating cells, the tumor microenvironment, and imaging findings as biomarkers of oligometastatic NSCLC. Biomarkers that help define true OMD and predict outcomes are needed for patient selection for oligometastatic treatment, and to avoid futile treatments in patients that will not benefit from locoregional treatment. Nevertheless, these biomarkers are still in the early stages of development and lack prospective validation in clinical trials. Furthermore, the absence of a clear definition of OMD contributes to a heterogeneous study population in which different types of OMD are mixed and treatment strategies are different. Multiple tissue-based, circulating, and imaging features are promising regarding their prognostic and predictive role in NSCLC, but data is still limited and might be biased owing to the inclusion of heterogeneous patient populations. Larger homogeneous and prospective series are needed to assess the prognostic and predictive role of these biomarkers. As obtaining tissue can be difficult and is invasive, the most promising tools for further evaluation are liquid biopsies and imaging-based biomarkers as these can also be used for longitudinal follow-up.
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来源期刊
CiteScore
4.20
自引率
0.00%
发文量
145
审稿时长
19 weeks
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