An overview of current advances of PD-L1 targeting immuno-imaging in cancers

J Cancer Res Ther. 2023 Aug;19(4):866-875. doi: 10.4103/jcrt.jcrt_88_23.

Abstract

The programmed death protein 1/programmed cell death ligand 1 (PD-1/PD-L1) pathway plays a significant role in immune evasion. PD-1 or PD-L1 immune checkpoint inhibitors (ICIs) have become a standard treatment for multiple types of cancer. To date, PD-L1 has served as a biomarker for predicting the efficacy of ICIs in several cancers. The need to establish an effective detection method that could visualize PD-L1 expression and predict the efficacy of PD-1/PD-L1 ICIs has promoted a search for new imaging strategies. PD-L1-targeting immuno-imaging could provide a noninvasive, real-time, repeatable, dynamic, and quantitative assessment of the characteristics of all tumor lesions in individual patients. This study analyzed the existing evidence in the literature on PD-L1-based immuno-imaging (2015-2022). Original English-language articles were searched using PubMed and Google Scholar. Keywords, such as "PD-L1," "PET," "SPECT," "PET/CT," and "SPECT/CT," were used in various combinations. A total of nearly 50 preclinical and clinical studies of PD-L1-targeting immuno-imaging were selected, reviewed, and included in this study. Therefore, in this review, we conducted a study of the advances in PD-L1-targeting immuno-imaging for detecting the expression of PD-L1 and the efficacy of ICIs. We focused on the different types of PD-L1-targeting agents, including antibodies and small PD-L1-binding agents, and illustrated the strength and weakness of these probes. Furthermore, we summarized the trends in the development of PD-L1-targeting immuno-imaging, as well as the current challenges and future directions for clinical workflow.

Keywords: Antibody; immuno-imaging; programmed cell death ligand 1; small binding agents.

Publication types

  • Review

MeSH terms

  • B7-H1 Antigen*
  • Humans
  • Immune Checkpoint Inhibitors
  • Neoplasms* / diagnostic imaging
  • Neoplasms* / drug therapy
  • Positron Emission Tomography Computed Tomography
  • Programmed Cell Death 1 Receptor
  • Tomography, Emission-Computed, Single-Photon

Substances

  • B7-H1 Antigen
  • Programmed Cell Death 1 Receptor
  • Immune Checkpoint Inhibitors