Sandro Pitigliani Medical Oncology Department, Prato Hospital, Istituto Toscano Tumori, Via Ugo Foscolo, Prato, PO 59100, Italy.
Translational Research Laboratory, Prato Hospital, Via Ugo Foscolo, Prato, PO 59100, Italy.
Cancers (Basel). 2014 Mar 25;6(2):684-707. doi: 10.3390/cancers6020684.
Circulating tumor cell (CTC) count has prognostic significance in metastatic breast cancer, but the predictive utility of CTCs is uncertain. Molecular studies on CTCs have often been limited by a low number of CTCs isolated from a high background of leukocytes. Improved enrichment techniques are now allowing molecular characterisation of single CTCs, whereby molecular markers on single CTCs may provide a real-time assessment of tumor biomarker status from a blood test or "liquid biopsy", potentially negating the need for a more invasive tissue biopsy. The predictive ability of CTC biomarker analysis has predominantly been assessed in relation to HER2, with variable and inconclusive results. Limited data exist for other biomarkers, such as the estrogen receptor. In addition to the need to define and validate the most accurate and reproducible method for CTC molecular analysis, the clinical relevance of biomarkers, including gain of HER2 on CTC after HER2 negative primary breast cancer, remains uncertain. This review summarises the currently available data relating to biomarker evaluation on CTCs and its role in directing management in metastatic breast cancer, discusses limitations, and outlines measures that may enable future development of this approach.
循环肿瘤细胞 (CTC) 计数在转移性乳腺癌中有预后意义,但 CTC 的预测效用尚不确定。由于白细胞背景中的 CTC 数量较少,对 CTC 的分子研究常常受到限制。改进的富集技术现在允许对单个 CTC 进行分子特征分析,从而单个 CTC 上的分子标记物可能提供来自血液检测或“液体活检”的肿瘤生物标志物状态的实时评估,从而可能无需进行更具侵袭性的组织活检。CTC 生物标志物分析的预测能力主要是在与 HER2 相关的情况下进行评估的,结果存在差异且不确定。其他生物标志物(如雌激素受体)的数据有限。除了需要定义和验证最准确和可重复的 CTC 分子分析方法外,生物标志物的临床相关性,包括 HER2 阴性原发性乳腺癌后 CTC 上 HER2 的获得,仍然不确定。这篇综述总结了目前关于 CTC 上的生物标志物评估及其在指导转移性乳腺癌管理中的作用的可用数据,讨论了局限性,并概述了可能使该方法得以进一步发展的措施。