Schelhaas Sonja, Heinzmann Kathrin, Bollineni Vikram R, Kramer Gerbrand M, Liu Yan, Waterton John C, Aboagye Eric O, Shields Anthony F, Soloviev Dmitry, Jacobs Andreas H
European Institute for Molecular Imaging (EIMI), Westfälische Wilhelms-Universität (WWU) Münster, Münster, Germany.
Comprehensive Cancer Imaging Centre, Imperial College London, UK.
Theranostics. 2017 Jan 1;7(1):40-50. doi: 10.7150/thno.16676. eCollection 2017.
The positron emission tomography (PET) tracer 3'-deoxy-3'-[F]fluorothymidine ([F]FLT) has been proposed to measure cell proliferation non-invasively . Hence, it should provide valuable information for response assessment to tumor therapies. To date, [F]FLT uptake has found limited use as a response biomarker in clinical trials in part because a better understanding is needed of the determinants of [F]FLT uptake and therapy-induced changes of its retention in the tumor. In this systematic review of preclinical [F]FLT studies, comprising 174 reports, we identify the factors governing [F]FLT uptake in tumors, among which thymidine kinase 1 plays a primary role. The majority of publications (83 %) report that decreased [F]FLT uptake reflects the effects of anticancer therapies. 144 times [F]FLT uptake was related to changes in proliferation as determined by analyses. Of these approaches, 77 % describe a positive relation, implying a good concordance of tracer accumulation and tumor biology. These preclinical data indicate that [F]FLT uptake holds promise as an imaging biomarker for response assessment in clinical studies. Understanding of the parameters which influence cellular [F]FLT uptake and retention as well as the mechanism of changes induced by therapy is essential for successful implementation of this PET tracer. Hence, our systematic review provides the background for the use of [F]FLT in future clinical studies.
正电子发射断层扫描(PET)示踪剂3'-脱氧-3'-[F]氟胸苷([F]FLT)已被提议用于非侵入性地测量细胞增殖。因此,它应为肿瘤治疗的疗效评估提供有价值的信息。迄今为止,[F]FLT摄取在临床试验中作为疗效生物标志物的应用有限,部分原因是需要更好地了解[F]FLT摄取的决定因素以及治疗引起的其在肿瘤中滞留的变化。在这项对174篇报告的临床前[F]FLT研究的系统评价中,我们确定了肿瘤中[F]FLT摄取的影响因素,其中胸苷激酶1起主要作用。大多数出版物(83%)报告称,[F]FLT摄取减少反映了抗癌治疗的效果。通过分析确定,[F]FLT摄取144次与增殖变化有关。在这些方法中,77%描述为正相关,这意味着示踪剂积聚与肿瘤生物学之间具有良好的一致性。这些临床前数据表明,[F]FLT摄取有望作为临床研究中疗效评估的成像生物标志物。了解影响细胞[F]FLT摄取和滞留的参数以及治疗引起的变化机制对于成功应用这种PET示踪剂至关重要。因此,我们 的系统评价为[F]FLT在未来临床研究中的应用提供了背景。