PD-L1
医学
正电子发射断层摄影术
伴生诊断
临床试验
肿瘤微环境
药物开发
癌症研究
肿瘤科
分子成像
免疫系统
癌症
免疫疗法
生物信息学
免疫检查点
内科学
药品
体内
核医学
药理学
免疫学
生物
生物技术
作者
David Leung,Samuel J. Bonacorsi,R. Adam Smith,Wolfgang Weber,Wendy Hayes
标识
DOI:10.3389/fonc.2021.698425
摘要
Programmed death-1 (PD-1) and programmed death ligand 1 (PD-L1) inhibitors target the important molecular interplay between PD-1 and PD-L1, a key pathway contributing to immune evasion in the tumor microenvironment (TME). Long-term clinical benefit has been observed in patients receiving PD-(L)1 inhibitors, alone and in combination with other treatments, across multiple tumor types. PD-L1 expression has been associated with response to immune checkpoint inhibitors, and treatment strategies are often guided by immunohistochemistry-based diagnostic tests assessing expression of PD-L1. However, challenges related to the implementation, interpretation, and clinical utility of PD-L1 diagnostic tests have led to an increasing number of preclinical and clinical studies exploring interrogation of the TME by real-time imaging of PD-(L)1 expression by positron emission tomography (PET). PET imaging utilizes radiolabeled molecules to non-invasively assess PD-(L)1 expression spatially and temporally. Several PD-(L)1 PET tracers have been tested in preclinical and clinical studies, with clinical trials in progress to assess their use in a number of cancer types. This review will showcase the development of PD-(L)1 PET tracers from preclinical studies through to clinical use, and will explore the opportunities in drug development and possible future clinical implementation.
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