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临床试验/NCT05111314
NCT05111314撤回1 期

Intraindividual Comparison of Hepatic Intraarterial Versus Systemic Intravenous 68Ga-PSMAPET/CT in Patients With HCC: Pilot Study

Mayo Clinic1 个研究点 分布在 1 个国家开始时间: 2022年2月11日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
撤回
发起方
Mayo Clinic
试验地点
1
主要终点
Intraindividual intralesional difference in maximum standardized uptake value (SUVmax)

研究概览

简要总结

This phase 0/1 study evaluates intraarterial administration of gallium Ga 68 gozetotide (68Ga-PSMA) for the detection of prostate-specific membrane antigen (PSMA) positive liver cancer by positron emission tomography (PET)/computed tomography (CT). 68Ga-PSMA is an imaging agent used with PET/CT scans to locate PSMA positive lesions. This study evaluates intraarterial administration of this agent, compared to intravenous administration.

详细描述

PRIMARY OBJECTIVE:

I. To determine the tumor radiotracer uptake (first pass effect or regional advantage) of direct hepatic intraarterial (I.A.) versus systemic intravenous (I.V.) 68Ga-PSMA in patients with PSMA+ hepatocellular carcinoma (HCC) by PET/CT.

OUTLINE:

Patients undergoing clinically indicated hepatic artery embolization will receive 68Ga-PSMA intraarterially (IA) over 5 minutes. After 60-90 minutes, patients undergo PET/CT scan over 1 hour.

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 —(Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Patients with either an imaging diagnosis of HCC by CT or magnetic resonance imaging (MRI) (Liver Imaging and Reporting Data System 5 [LI-RADS 5]) confirmed by a board-certified abdominal radiologist, or with biopsy-proven HCC
  • •Already enrolled in ongoing Transform the Practice or Department of Defense 68Ga-PSMA studies
  • •PSMA avid HCC detected by 68Ga-PSMA PET/CT after intravenous administration of 68Ga-PSMA confirmed by a board certified nuclear radiologist
  • •Undergoing planned hepatic artery embolization (HAE) per standard clinical care
  • •Male or female with age greater than 18 years, with the capacity and willingness to provide a written informed consent

排除标准

  • •Subjects requiring emergent surgery for a ruptured/bleeding HCC
  • •Pregnant and/or breast-feeding subjects. A negative pregnancy test within 48 hours of the PET scan
  • •Subjects with higher than the weight/size limitations of PET/CT scanner

研究组 & 干预措施

Diagnostic (embolization, 68Ga-PSMA, PET/CT)

Experimental

Patients undergoing clinically indicated hepatic artery embolization will receive 68Ga-PSMA intraarterially (IA) over 5 minutes. After 60-90 minutes, patients undergo PET/CT scan over 1 hour.

干预措施: Gallium Ga 68 Gozetotide (Radiation)

Diagnostic (embolization, 68Ga-PSMA, PET/CT)

Experimental

Patients undergoing clinically indicated hepatic artery embolization will receive 68Ga-PSMA intraarterially (IA) over 5 minutes. After 60-90 minutes, patients undergo PET/CT scan over 1 hour.

干预措施: Hepatic Artery Embolization (Procedure)

Diagnostic (embolization, 68Ga-PSMA, PET/CT)

Experimental

Patients undergoing clinically indicated hepatic artery embolization will receive 68Ga-PSMA intraarterially (IA) over 5 minutes. After 60-90 minutes, patients undergo PET/CT scan over 1 hour.

干预措施: Positron Emission Tomography and Computed Tomography Scan (Procedure)

结局指标

主要结局

Intraindividual intralesional difference in maximum standardized uptake value (SUVmax)

时间窗: Up to 2 years

Intraindividual intralesional difference in maximum standardized uptake value (SUVmax) will be evaluated as fold change and absolute difference for a given lesion between intra-arterially (I.A.) and intravenous (I.V.) prostate-specific membrane antigen (PSMA) positron emission tomography (PET). Qualitative evaluation assesses the intensity of PSMA uptake in hepatic lesions, graded as follows: grade 1: uptake \< normal liver; grade 2: uptake = normal liver; grade 3: uptake \> normal liver; grade 4: uptake \> spleen or kidneys. Semi-quantitative analysis is undertaken by calculating intraindividual difference in SUVmax for each lesion between I.A. and I.V. PSMA PET followed by a two-sided one sample t-test. Maximum and mean standardized uptake value (SUVmax, SUVmean, SUVmin) of the lesion(s), and SUVmax of the background liver are noted.

次要结局

  • Incidence of adverse events(Up to 2 years)
  • Intraindividual intralesional differences in tumor to background (TBR) of SUVmax(Up to 2 years)
  • Difference in PSMA uptake measured by SUVmax (fold change, absolute difference) in the kidneys, spleen and salivary glands between I.A. and I.V. PSMA PET.(Up to 2 years)

研究者

发起方
Mayo Clinic
申办方类型
Other
责任方
Principal Investigator
主要研究者

Scott M. Thompson

Principal Investigator

Mayo Clinic

研究点 (1)

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