跳至主要内容
临床试验/NCT07023640
NCT07023640招募中不适用

Application of the CD73-Targeted Probe ⁶⁸Ga-DOTA-mPNE PET/CT Imaging in the Diagnosis of Malignant Tumors

Peking Union Medical College Hospital1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年7月10日最近更新:

试验速览

阶段
不适用
状态
招募中
入组人数
50
试验地点
1
主要终点
SUVmax

研究概览

简要总结

This study aims to perform ⁶⁸Ga-DOTA-mPNE PET/CT imaging in patients with clinically suspected or confirmed malignant tumors, in order to evaluate tracer uptake in lesions and analyze CD73 expression levels. In a subgroup of up to 10 participants, dynamic PET/CT imaging will be conducted for up to 90 minutes post-injection to assess the tracer's biodistribution and pharmacokinetic properties.Correlation analyses with relevant clinical indicators (such as pathology, immunohistochemistry, and molecular markers) will be carried out to further assess the diagnostic performance and clinical value of ⁶⁸Ga-DOTA-mPNE PET/CT in guiding tumor diagnosis and treatment. This study is expected to provide a novel molecular imaging tool for malignancies and offer clear, intuitive PET/CT-based evidence to support clinical diagnosis, differential diagnosis, and therapeutic decision-making.

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 70 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Age ≥18 years, with an expected survival of ≥12 weeks.
  • No prior radiotherapy or chemotherapy; eligible for surgery or biopsy to obtain pathological diagnosis.
  • At least one measurable target lesion according to RECIST version 1.1 (Response Evaluation Criteria in Solid Tumors).
  • Written informed consent obtained and able to comply with follow-up requirements.

排除标准

  • Severe hepatic or renal dysfunction.
  • Women who are planning to conceive, currently pregnant, breastfeeding, or intend to have children during the study period are not eligible. Fertile participants must use effective contraception during the study.
  • Unable to lie flat for 30 minutes.
  • Refusal to participate in this clinical study.
  • Claustrophobia or other psychiatric disorders.
  • Any other condition deemed unsuitable for study participation by the investigator.

结局指标

主要结局

SUVmax

时间窗: Time Frame: Day 1 (on the day of PET/CT imaging)

The area of interest was delineated and the SUVmax value was measured by using the post-processing software built into the acquisition machine.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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