Preclinical and exploratory human studies of novel 68Ga-labeled D-peptide antagonist for PET imaging of TIGIT expression in cancers

Purpose While TIGIT has been propelled as a next-generation target in cancer immunotherapy, anti-TIGIT therapy seems to be promising for a fraction of patients in clinical trials. Therefore, patient stratification is critical for this therapy, which could benefit from a whole-body, non-invasive, and quantitative evaluation of TIGIT expression in cancers. In this study, a Ga-68-labeled D-peptide antagonist, Ga-68-GP12, was developed and validated for PET imaging of TIGIT expression in vitro, in vivo, and in an exploratory human study. Methods The D-enantiomer peptide antagonists were modified and radiolabeled with Ga-68. In vitro binding assays were performed in human peripheral blood mononuclear cells (PBMCs) to assess their affinity and specificity. The imaging capacity, biodistribution, pharmacokinetics, and radiation dosimetry were investigated. Flow cytometry, autoradiography, and immunohistochemical staining were used to confirm the expression of TIGIT. The safety and potential of Ga-68-GP12 for PET/CT imaging of TIGIT expression were evaluated in NSCLC patients. Results Ga-68-labeled D-peptides were conveniently produced with high radiochemical yields, radiochemical purities and molar activities. In vitro binding assays demonstrated Ga-68-GP12 has high affinity and specificity for TIGIT with a K-D of 37.28 nM. In vivo and ex vivo studies demonstrated the capacity of Ga-68-GP12 for PET imaging of TIGIT expression with high tumor uptake of 4.22 +/- 0.68 %ID/g and the tumor-to-muscle ratio of 12.94 +/- 2.64 at 60 min post-injection. In NSCLC patients, primary and metastatic lesions found in Ga-68-GP12 PET images were comparable to that in F-18-FDG PET images. Moreover, tracer uptake in primary and metastatic lesions and intra-tumoral distribution in the large tumor were inhomogenous, indicating the heterogeneity of TIGIT expression. Conclusion Ga-68-GP12 is a promising radiotracer for PET imaging of TIGIT expression in cancers, indicating its potential as a potential companion diagnostic for anti-TIGIT therapies.