[68Ga]Ga-RAYZ-8009: A Glypican-3–Targeted Diagnostic Radiopharmaceutical for Hepatocellular Carcinoma Molecular Imaging—A First-in-Human Case Series

Alex J. Poot, Constantin Lapa, Wolfgang A. Weber, Marnix G.E.H. Lam, Matthias Eiber, Alexander Dierks, Ralph A. Bundschuh, Arthur J.A.T. Braat
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Abstract

To date, the imaging and diagnosis of hepatocellular carcinoma (HCC) rely on CT/MRI, which have well-known limitations. Glypican-3 (GPC3) is a cell surface receptor highly expressed by HCC but not by normal or cirrhotic liver tissue. Here we report initial clinical results of GPC3-targeted PET imaging with [68Ga]Ga-DOTA-RYZ-GPC3 (RAYZ-8009), a peptide-based GPC3 ligand in patients with known or suspected HCC. Methods: [68Ga]Ga-RAYZ-8009 was obtained after labeling the peptide precursor with 68Ga from a 68Ge/68Ga generator and heating at 90°C for 10 min followed by sterile filtration. After administration of [68Ga]Ga-RAYZ-8009, a dynamic or static PET/CT scan was acquired between 45 min and 4 h after administration. Radiotracer uptake was measured by SUVs for the following tissues: suspected or actual HCC or hepatoblastoma lesions, non–tumor-bearing liver, renal cortex, blood pool in the left ventricle, and gastric fundus. Additionally, tumor–to–healthy-liver ratios (TLRs) were calculated. Results: Twenty-four patients (5 patients in the dynamic protocol; 19 patients in the static protocol) were scanned. No adverse events occurred. Two patients had no lesion detected and did not have HCC during follow-up. In total, 50 lesions were detected and analyzed. The mean SUVmax of these lesions was 19.6 (range, 2.7–95.3), and the mean SUVmean was 10.1 (range, 1.0–49.2) at approximately 60 min after administration. Uptake in non–tumor-bearing liver and blood pool rapidly decreased over time and became negligible 45 min after administration (mean SUVmean, <1.6), with a continuous decline to 4 h after administration (mean SUVmean, 1.0). The opposite was observed for HCC lesions, for which SUVs and TLRs continuously increased for up to 4 h after administration. In individual lesion analysis, TLR was the highest between 60 and 120 min after administration. Uptake in the gastric fundus gradually increased for up to 45 min (to an SUVmax of 31.3) and decreased gradually afterward. Conclusion: [68Ga]Ga-RAYZ-8009 is safe and allows for high-contrast imaging of GPC3-positive HCC, with rapid clearance from most normal organs. Thereby, [68Ga]Ga-RAYZ-8009 is promising for HCC diagnosis and staging. Further research is warranted.

[68Ga]Ga-RAYZ-8009:用于肝细胞癌分子成像的 Glypican-3 靶向诊断放射性药物--首个人体病例系列
迄今为止,肝细胞癌(HCC)的成像和诊断主要依靠 CT/MRI,而 CT/MRI 具有众所周知的局限性。Glypican-3(GPC3)是一种细胞表面受体,在 HCC 中高度表达,但在正常或肝硬化肝组织中却不表达。我们在此报告使用[68Ga]Ga-DOTA-RYZ-GPC3 (RAYZ-8009)(一种基于多肽的 GPC3 配体)对已知或疑似 HCC 患者进行 GPC3 靶向 PET 成像的初步临床结果。方法:[68Ga]Ga-RAYZ-8009 是用 68Ge/68Ga 发生器中的 68Ga 标记多肽前体后,在 90°C 下加热 10 分钟,然后进行无菌过滤而得到的。给药[68Ga]Ga-RAYZ-8009后,在给药后45分钟至4小时之间进行动态或静态PET/CT扫描。通过 SUV 测量以下组织的放射性示踪剂摄取量:疑似或实际的 HCC 或肝母细胞瘤病灶、无瘤肝脏、肾皮质、左心室血池和胃底。此外,还计算了肿瘤与健康肝脏的比率(TLRs)。结果共对 24 名患者进行了扫描(5 名患者采用动态方案;19 名患者采用静态方案)。无不良事件发生。两名患者未检测到病变,随访期间也未出现 HCC。总共检测和分析了 50 个病灶。用药后约 60 分钟,这些病灶的平均 SUVmax 为 19.6(范围为 2.7-95.3),平均 SUVmean 为 10.1(范围为 1.0-49.2)。随着时间的推移,非肿瘤肝脏和血池中的摄取量迅速下降,在给药后 45 分钟变得微不足道(平均 SUVmean 为 1.6),并持续下降至给药后 4 小时(平均 SUVmean 为 1.0)。而 HCC 病变的情况恰恰相反,给药后 4 小时内 SUV 和 TLRs 持续上升。在单个病灶分析中,TLR 在用药后 60 至 120 分钟内最高。胃底的摄取量在 45 分钟内逐渐增加(SUVmax 为 31.3),之后逐渐降低。结论[68Ga]Ga-RAYZ-8009是安全的,可对GPC3阳性的HCC进行高对比度成像,并能迅速从大多数正常器官中清除。因此,[68Ga]Ga-RAYZ-8009有望用于HCC诊断和分期。有必要开展进一步的研究。
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