First-in-Human Study of the Radioligand 68Ga-N188 Targeting Nectin-4 for PET/CT Imaging of Advanced Urothelial Carcinoma

医学 连接蛋白 生物标志物 癌症 靶向治疗 药代动力学 免疫组织化学 PET-CT 病理 肿瘤科 内科学 正电子发射断层摄影术 核医学 细胞 生物 细胞粘附 生物化学 遗传学
作者
Xiaojiang Duan,Lei Xia,Zhuochen Zhang,Yanan Ren,Martin G. Pomper,Steven P. Rowe,Xuesong Li,Nan Li,Ning Zhang,Hua Zhu,Zhi Yang,Xinan Sheng,Xing Yang
出处
期刊:Clinical Cancer Research [American Association for Cancer Research]
卷期号:29 (17): 3395-3407 被引量:12
标识
DOI:10.1158/1078-0432.ccr-23-0609
摘要

Abstract Purpose: Nectin-4 is an emerging biomarker for cancer diagnosis and therapy. Recently, enfortumab vedotin (EV) was approved by the FDA as the first nectin-4 targeting antibody–drug conjugate for treating advanced urothelial carcinoma (UC). A PET imaging method to noninvasively quantify nectin-4 expression level would potentially help to select patients most likely to respond to EV and predict the response. Experimental Design: In this study, we designed a bicyclic peptide-based nectin-4 targeting radiotracer 68Ga-N188. Initially, we performed preclinical evaluations of 68Ga-N188 in UC cell lines and xenograft mouse models. Next, we performed the translational study in healthy volunteers and a pilot cohort of patients with advanced UC on uEXPLORER total-body PET/CT. Results: In the preclinical study, 68Ga-N188 showed high affinity to nectin-4, specific uptake in a nectin-4(+) xenograft mouse model, and suitable pharmacokinetic and safety profiles. In the translational study, 2 healthy volunteers and 14 patients with advanced UC were enrolled. The pharmacokinetic profile was determined for 68Ga-N188, and the nectin-4 relative expression level in different organs was quantitatively imaged. Conclusions: A clear correlation between PET SUV value and nectin-4 expression was observed, supporting the application of 68Ga-N188 PET as a companion diagnostic tool for optimizing treatments that target nectin-4. See related commentary by Jiang et al., p. 3259
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