Tomaszewski Michal R, Gonzalez Isabel Quiros, O'Connor James Pb, Abeyakoon Oshaani, Parker Geoff Jm, Williams Kaye J, Gilbert Fiona J, Bohndiek Sarah E
Department of Physics, University of Cambridge, U.K.
Cancer Research UK Cambridge Institute, University of Cambridge, U.K.
Theranostics. 2017 Jul 8;7(11):2900-2913. doi: 10.7150/thno.19841. eCollection 2017.
Poor oxygenation of solid tumours has been linked with resistance to chemo- and radio-therapy and poor patient outcomes, hence non-invasive imaging of oxygen supply and demand in tumours could improve disease staging and therapeutic monitoring. Optoacoustic tomography (OT) is an emerging clinical imaging modality that provides static images of endogenous haemoglobin concentration and oxygenation. Here, we demonstrate oxygen enhanced (OE)-OT, exploiting an oxygen gas challenge to visualise the spatiotemporal heterogeneity of tumour vascular function. We show that tracking oxygenation dynamics using OE-OT reveals significant differences between two prostate cancer models in nude mice with markedly different vascular function (PC3 & LNCaP), which appear identical in static OT. LNCaP tumours showed a spatially heterogeneous response within and between tumours, with a substantial but slow response to the gas challenge, aligned with analysis, which revealed a generally perfused and viable tumour with marked areas of haemorrhage. PC3 tumours had a lower fraction of responding pixels compared to LNCaP with a high disparity between rim and core response. While the PC3 core showed little or no dynamic response, the rim showed a rapid change, consistent with our findings of hypoxic and necrotic core tissue surrounded by a rim of mature and perfused vasculature. OE-OT metrics are shown to be highly repeatable and correlate directly on a per-tumour basis to tumour vessel function assessed OE-OT provides a non-invasive approach to reveal the complex dynamics of tumour vessel perfusion, permeability and vasoactivity in real time. Our findings indicate that OE-OT holds potential for application in prostate cancer patients, to improve delineation of aggressive and indolent disease as well as in patient stratification for chemo- and radio-therapy.
实体肿瘤的低氧状态与化疗和放疗耐药以及患者预后不良有关,因此对肿瘤氧供需进行无创成像可改善疾病分期和治疗监测。光声断层扫描(OT)是一种新兴的临床成像方式,可提供内源性血红蛋白浓度和氧合的静态图像。在此,我们展示了氧增强(OE)-OT,利用氧气激发来可视化肿瘤血管功能的时空异质性。我们表明,使用OE-OT追踪氧合动力学可揭示裸鼠中两种具有明显不同血管功能的前列腺癌模型(PC3和LNCaP)之间的显著差异,而在静态OT中它们看起来是相同的。LNCaP肿瘤在肿瘤内部和之间表现出空间异质性反应,对气体激发的反应强烈但缓慢,这与分析结果一致,分析显示该肿瘤总体灌注良好且存活,但有明显出血区域。与LNCaP相比,PC3肿瘤的反应像素比例较低,边缘和核心反应之间存在很大差异。虽然PC3肿瘤核心几乎没有或没有动态反应,但边缘显示出快速变化,这与我们发现的缺氧和坏死核心组织被成熟且灌注良好的血管边缘包围的结果一致。结果表明,OE-OT指标具有高度可重复性,并且在每个肿瘤基础上与通过[未提及的评估方法]评估的肿瘤血管功能直接相关。OE-OT提供了一种无创方法来实时揭示肿瘤血管灌注、通透性和血管活性的复杂动态。我们的研究结果表明,OE-OT在前列腺癌患者中具有应用潜力,可改善侵袭性和惰性疾病的 delineation 以及化疗和放疗的患者分层。 (注:原文中“aligned with analysis”和“assessed ”部分信息缺失,翻译时保留原文形式)