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临床试验/NCT07254104
NCT07254104Enrolling By Invitation1 期

Clinical Evaluation of [68Ga]Ga-NOTA-RF PET Imaging Targeting RFVT3 in Patients With Pituitary Tumors

Peking Union Medical College Hospital1 个研究点 分布在 1 个国家目标入组 30 人开始时间: 2025年11月17日最近更新:
干预措施

试验速览

阶段
1 期
状态
Enrolling By Invitation
入组人数
30
试验地点
1
主要终点
SUVmax

研究概览

简要总结

This study aims to evaluate the clinical application value of [68Ga]Ga-NOTA-RF, a novel PET molecular probe targeting riboflavin transporter 3 (RFVT3), in patients with pituitary adenomas. It will observe the probe's imaging characteristics, distribution signs, and the relationships between these factors, tumor differentiation degree, and radiotracer uptake. Additionally, the study will explore the diagnostic advantages of [68Ga]Ga-NOTA-RF in patients with pituitary adenomas and its potential value in precise typing.

详细描述

This study aims to evaluate the potential clinical application of [68Ga]Ga-NOTA-RF in pituitary adenomas. Such tumors are characterized by variable degrees of differentiation, subtle early morphological changes, complex metabolic states, and a strong dependence on mitochondrial activity. Existing imaging modalities have limited performance in detecting and characterizing these lesions, highlighting the need for novel metabolic imaging tools. This study will systematically investigate the biodistribution and imaging characteristics of [68Ga]Ga-NOTA-RF in pituitary adenomas, as well as its correlation with RFVT3 expression, to explore its potential value in early tumor detection, metabolic subtype differentiation, and molecular classification.

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

入选标准

  • Age between 18 and 80 years, male or female.
  • Able to understand and sign written informed consent, willing to follow pre-injection preparation requirements (adequate hydration and avoidance of high-dose riboflavin supplements), and to complete all study procedures.
  • Recurrent invasive pituitary adenoma within 6 months after surgery, without intracranial or distant metastasis. The postoperative pathological Ki-67 index of the previous pituitary tumor is ≥3%, and tumor growth cannot be controlled by standard medical therapy and radiotherapy.
  • Radiological and clinical evidence indicates residual or recurrent pituitary adenoma requiring treatment or follow-up management.
  • At least one measurable and resectable lesion suitable for correlation with PET imaging evaluation; vital signs are stable, and the participant is able to lie supine and cooperate during a 30-60 minute PET scan.

排除标准

  • Pregnant or planning to become pregnant, or breastfeeding women.
  • Known history of severe allergic or anaphylactoid reactions to any component of the investigational tracer (riboflavin derivatives, NOTA chelator, or formulation excipients).
  • Presence of severe or uncontrolled medical conditions (e.g., decompensated heart failure, active infection, myocardial infarction or stroke within the past 4 weeks) that, in the opinion of the investigator, make the participant unsuitable for PET imaging.
  • Concomitant severe systemic diseases such as cardiac, pulmonary, hepatic, or renal failure.
  • Pituitary adenoma patients who underwent surgery less than 4 weeks prior to enrollment or completed radiotherapy to the sellar region within the past 3 months.
  • Participation in another interventional clinical trial within the past 4 weeks, or cumulative radiation exposure from prior research procedures within the past 12 months that may exceed the ethical safety limit.
  • Severe claustrophobia unrelieved by sedation, or any other condition that would prevent completion of the PET scan.
  • Poor compliance or any factor judged by the investigator to affect the participant's safety or the quality of study data.
  • Any other condition that, in the judgment of the investigator, makes the participant unsuitable for study participation.

研究组 & 干预措施

Pituitary Neoplasms

Experimental

Participants with pituitary neoplasms will undergo [68Ga]Ga-NOTA-RF PET/CT imaging to evaluate tracer uptake, biodistribution, and safety.

干预措施: [68Ga]Ga-NOTA-RF (Drug)

结局指标

主要结局

SUVmax

时间窗: After the completion of the PET examination.

The tumor uptake capacity (expressed as SUV values) of \[68Ga\]Ga-NOTA-RF PET imaging in intracranial tumors.

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Xianzhong Zhang

Professor

Peking Union Medical College Hospital

研究点 (1)

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