Stumpo Vittorio, Guida Lelio, Bellomo Jacopo, Van Niftrik Christiaan Hendrik Bas, Sebök Martina, Berhouma Moncef, Bink Andrea, Weller Michael, Kulcsar Zsolt, Regli Luca, Fierstra Jorn
Department of Neurosurgery, University Hospital Zurich, 8091 Zurich, Switzerland.
Clinical Neuroscience Center, University Hospital Zurich, University of Zurich, 8057 Zurich, Switzerland.
Cancers (Basel). 2022 Mar 5;14(5):1342. doi: 10.3390/cancers14051342.
Gliomas, and glioblastoma in particular, exhibit an extensive intra- and inter-tumoral molecular heterogeneity which represents complex biological features correlating to the efficacy of treatment response and survival. From a neuroimaging point of view, these specific molecular and histopathological features may be used to yield imaging biomarkers as surrogates for distinct tumor genotypes and phenotypes. The development of comprehensive glioma imaging markers has potential for improved glioma characterization that would assist in the clinical work-up of preoperative treatment planning and treatment effect monitoring. In particular, the differentiation of tumor recurrence or true progression from pseudoprogression, pseudoresponse, and radiation-induced necrosis can still not reliably be made through standard neuroimaging only. Given the abundant vascular and hemodynamic alterations present in diffuse glioma, advanced hemodynamic imaging approaches constitute an attractive area of clinical imaging development. In this context, the inclusion of objective measurable glioma imaging features may have the potential to enhance the individualized care of diffuse glioma patients, better informing of standard-of-care treatment efficacy and of novel therapies, such as the immunotherapies that are currently increasingly investigated. In Part B of this two-review series, we assess the available evidence pertaining to hemodynamic imaging for molecular feature prediction, in particular focusing on isocitrate dehydrogenase (IDH) mutation status, MGMT promoter methylation, 1p19q codeletion, and EGFR alterations. The results for the differentiation of tumor progression/recurrence from treatment effects have also been the focus of active research and are presented together with the prognostic correlations identified by advanced hemodynamic imaging studies. Finally, the state-of-the-art concepts and advancements of hemodynamic imaging modalities are reviewed together with the advantages derived from the implementation of radiomics and machine learning analyses pipelines.
胶质瘤,尤其是胶质母细胞瘤,表现出广泛的肿瘤内和肿瘤间分子异质性,这代表了与治疗反应疗效和生存相关的复杂生物学特征。从神经影像学角度来看,这些特定的分子和组织病理学特征可用于产生成像生物标志物,作为不同肿瘤基因型和表型的替代指标。全面的胶质瘤成像标志物的开发具有改善胶质瘤特征描述的潜力,这将有助于术前治疗规划和治疗效果监测的临床检查。特别是,仅通过标准神经影像学仍无法可靠地区分肿瘤复发或真正进展与假性进展、假性反应和放射性坏死。鉴于弥漫性胶质瘤中存在丰富的血管和血流动力学改变,先进的血流动力学成像方法构成了临床成像发展的一个有吸引力的领域。在这种情况下,纳入客观可测量的胶质瘤成像特征可能有潜力加强弥漫性胶质瘤患者的个体化护理,更好地了解标准治疗疗效和新疗法,如目前越来越受研究的免疫疗法。在这个两篇综述系列的B部分中,我们评估了有关血流动力学成像用于分子特征预测的现有证据,特别关注异柠檬酸脱氢酶(IDH)突变状态、MGMT启动子甲基化、1p19q共缺失和表皮生长因子受体(EGFR)改变。区分肿瘤进展/复发与治疗效果的结果也是积极研究的重点,并与先进血流动力学成像研究确定的预后相关性一起呈现。最后,回顾了血流动力学成像模式的最新概念和进展,以及从实施放射组学和机器学习分析管道中获得的优势。