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神经内分泌肿瘤中生长抑素类似物、肽受体放射性核素治疗和血清素途径靶点的预后和预测生物标志物。

Prognostic and predictive biomarkers for somatostatin analogs, peptide receptor radionuclide therapy and serotonin pathway targets in neuroendocrine tumours.

机构信息

Division of Cancer Sciences, School of Medical Sciences, Faculty of Biology, Medicine and Health, University of Manchester, The Christie ENETS Centre of Excellence, UK.

Medical Oncology Department, Hospital Universitario La Paz, CIBERONC CB16/12/00398, Madrid, Spain.

出版信息

Cancer Treat Rev. 2018 Nov;70:209-222. doi: 10.1016/j.ctrv.2018.09.008. Epub 2018 Sep 26.

Abstract

Neuroendocrine tumours (NETs) are a heterogeneous group of neoplasms regarding their molecular biology, clinical behaviour, prognosis and response to therapy. Several attempts to establish robust predictive biomarkers have failed. Neither tissue markers nor blood borne ones have proven to be successful yet. Circulating tumour cells (CTCs) as "liquid biopsies" could provide prognostic information at the time a therapeutic decision needs to be made and could be an attractive tool for tumour monitoring throughout the treatment period. However, "liquid biopsies" are far from becoming the standard biomarker in NETs. Promising results have been presented over the last few years using a novel biomarker candidate, a multianalyte algorithm analysis PCR-based test (NETest). New technologies will open the field to different ways of approaching the biomarker conundrum in NETs. However, the complications derived from being a heterogeneous group of malignancies will remain with us forever. In summary, there is an unmet need to incorporate new biomarker candidates into clinical research trials to obtain a robust prospective validation under the most demanding scenario.

摘要

神经内分泌肿瘤(NETs)在分子生物学、临床行为、预后和对治疗的反应方面存在异质性。尽管人们曾多次尝试建立可靠的预测性生物标志物,但都没有成功。组织标志物和血液标志物都尚未被证明是有效的。循环肿瘤细胞(CTC)作为“液体活检”,可以在需要做出治疗决策时提供预后信息,并可能成为治疗期间肿瘤监测的一种有吸引力的工具。然而,“液体活检”还远未成为 NETs 的标准生物标志物。在过去的几年中,使用一种新的生物标志物候选物,即基于多分析物算法分析的聚合酶链反应(NETest)检测,已经提出了有希望的结果。新技术将为 NETs 中的生物标志物难题开辟不同的方法。然而,作为一组异质性恶性肿瘤,其复杂性将永远伴随着我们。总之,需要将新的生物标志物候选物纳入临床研究试验中,以便在最苛刻的情况下进行强有力的前瞻性验证。

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