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临床试验/NCT07677774
NCT07677774招募中不适用

Glypian-3 (GPC3)- Targeted PET Imaging in Hepatocellular Carcinoma

The First Affiliated Hospital of Xiamen University1 个研究点 分布在 1 个国家目标入组 40 人开始时间: 2026年5月1日最近更新:
适应症
干预措施

试验速览

阶段
不适用
状态
招募中
入组人数
40
试验地点
1
主要终点
Diagnostic efficacy

研究概览

简要总结

The objective of the study is to evaluate the diagnostic value of GPC3-targeted PET/CT in patients with suspected or histologically/clinically confirmed hepatocellular carcinoma, and to compare with contrast-enhanced MRI.

详细描述

This study is designed to investigate GPC3-targeted PET/CT as a noninvasive approach for detecting tumor lesions in patients with suspected or histologically/clinically confirmed hepatocellular carcinoma. In this research, eligible patients will undergo contemporaneous GPC3-targeted PET/CT and contrast-enhanced liver MRI plus conventional extrahepatic imaging either for initial assessment or for metastases or highly suspected recurrence detection. Tumor uptake will be quantified by the maximum standardized uptake value (SUVmax). Positive lesions detected by contrast-enhanced liver MRI + conventional imaging and GPC3-targeted PET/CT will be recorded by visual interpretation and compared. Imaging findings will be compared with pathological result and/or a composite reference standard incorporating radiologic follow-up, clinical course, and treatment response..

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 90 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Adult patients (aged 18 years or older);
  • Patients with suspected, newly diagnosed, or previously treated hepatocellular carcinoma(supporting evidence may include imaging findings and pathology report);
  • Patients who were able to provide informed consent (signed by participant, parent or legal representative) and assent according to the guidelines of the Clinical Research Ethics Committee.
  • Estimated life expectancy of more than 3 months, as assessed by the investigator, and ability to comply with study procedures and scheduled visits;

排除标准

  • Lack of contrast-enhanced liver MRI or an interval of more than 14 days between GPC3-targeted PET/CT and contrast-enhanced liver MRI.
  • Receipt of antitumor treatment between imaging examinations.
  • The inability or unwillingness of the research participant or legal representative to provide written informed consent.
  • Inability to complete PET/CT imaging.

研究组 & 干预措施

GPC3-targeted PET/CT

Experimental

Each subject receives a single intravenous injection of GPC3-targeted probe and undergoes PET/CT imaging within the specified time.

干预措施: GPC3-targeted PET/CT (Diagnostic Test)

结局指标

主要结局

Diagnostic efficacy

时间窗: 1 year

The sensitivity, specificity, and accuracy of 18F-FDG PET/CT and GPC3-targeted PET/CT were calculated and compared to evaluate the diagnostic accuracy.

Diagnostic accuracy

时间窗: 1 year

The sensitivity, specificity, and accuracy of GPC3-targeted PET/CT and CE-MRI in detecting malignant hepatic lesions were calculated and compared.

次要结局

  • Gastric SUVmax Stratified by Gastric Filling Status(1 day)
  • Agreement of BCLC classification with the reference classification(1 year)
  • Lesion detection by GPC3-targeted PET/CT compared with 18F-FDG PET/CT(Within 14 days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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