Wu Minghao, Zhang Yanyan, Zhang Yuwei, Liu Ying, Wu Mingjie, Ye Zhaoxiang
Department of Radiology, Tianjin Medical University Cancer Institute and Hospital, National Clinical Research Center for Cancer, Tianjin's Clinical Research Center for Cancer Key Laboratory of Cancer Prevention and Therapy, Huanhuxi Road, Hexi District, Tianjin 300060, PR China (M.W., Y.Z., Y. Z., Y.L., Z.Y.); and Institut National de la Recherche Scientifique-Énergie Matériaux et Télécommunications, Varennes, Quebec, Canada (Mingjie Wu).
Radiol Imaging Cancer. 2019 Nov 29;1(2):e190031. doi: 10.1148/rycan.2019190031. eCollection 2019 Nov.
Proper patient selection for immunotherapy is critical, as certain tumor microenvironments are more permissible to therapy than others. Currently, the use of programmed cell death ligand-1 (PD-L1) and microsatellite instability high and/or mismatch repair deficiency are used as biomarkers for immunotherapy response. To improve tumor characterization, methodologies are being developed to combine imaging with tumor immune environment characterization. Imaging of tumors from immunotherapy responders and nonresponders with various imaging modalities has led to the development of criteria that could predict patient response to immunotherapy. Additionally, radiomics-based artificial intelligence methods are being used to characterize tumor microenvironments to predict and evaluate immunotherapy responses, as well as to predict risk of immune-related adverse events. Molecular imaging techniques are also being developed for various modalities to observe tumor expression of immunotherapy targets, such as PD-L1 and, to confirm the target is being expressed on resident tumors. In all, the advancements of imaging techniques to define tumor immunologic characteristics will help to stratify patients who are more likely to respond to immunotherapies. Computer Aided Diagnosis (CAD), Computer Applications-Virtual Imaging, Efficacy Studies, MR-Imaging, Molecular Imaging-Cancer, Molecular Imaging-Immunotherapy, Molecular Imaging-Nanoparticles, Molecular Imaging-Probe Development, Molecular Imaging-Target Development, SPECT/CT © RSNA, 2019.
正确选择免疫治疗的患者至关重要,因为某些肿瘤微环境比其他微环境更适合进行治疗。目前,程序性细胞死亡配体1(PD-L1)以及微卫星高度不稳定和/或错配修复缺陷被用作免疫治疗反应的生物标志物。为了改善肿瘤特征描述,正在开发将成像与肿瘤免疫环境特征描述相结合的方法。使用各种成像方式对免疫治疗反应者和无反应者的肿瘤进行成像,已促成了可预测患者免疫治疗反应的标准的制定。此外,基于放射组学的人工智能方法正被用于描述肿瘤微环境,以预测和评估免疫治疗反应,以及预测免疫相关不良事件的风险。还在为各种成像方式开发分子成像技术,以观察免疫治疗靶点(如PD-L1)在肿瘤中的表达,并确认该靶点在驻留肿瘤上的表达情况。总之,用于定义肿瘤免疫特征的成像技术的进步将有助于对更可能对免疫治疗产生反应的患者进行分层。计算机辅助诊断(CAD)、计算机应用 - 虚拟成像、疗效研究、磁共振成像、分子成像 - 癌症、分子成像 - 免疫治疗、分子成像 - 纳米颗粒、分子成像 - 探针开发、分子成像 - 靶点开发、SPECT/CT © RSNA,2019年