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68Ga-C1 PET/ CT Imaging in Clear Cell Renal Cell Carcinoma

Not Applicable
Recruiting
Conditions
Carbonic Anhydrase IX
Clear Cell Renal Cell Carcinoma
PET-CT
Interventions
Registration Number
NCT06519760
Lead Sponsor
Peking University First Hospital
Brief Summary

The goal of this clinical trial is to evaluate the diagnostic value of CAIX protein specific probe 68Ga-C1 in PET/CT imaging in clear cell renal cell carcinoma patients. It will also learn about the safety, tolerability and radiation dosimetry of 68Ga-C1.

Researchers will compare the diagnostic value of 68Ga-C1 PET/CT and 18F-FDG PET/CT in Chinese patients with indeterminate renal masses or confirmed clear cell renal cell carcinoma.

Detailed Description

Carbonic anhydrase IX (CAIX) is a transmembrane protein which is highly expressed in approximately 95% of clear cell renal cell carcinomas, and it is closely related to tumor progression, patients prognosis and treatment response. Here, we developed a CAIX specific small molecule probe 68Ga-C1, which has shown a good diagnostic accuracy in PET/CT imaging in our preclinical mouse model of clear cell renal cell carcinoma. This enables high-contrast imaging of clear cell renal carcinoma, providing a new imaging method for the precise diagnosis of clear cell renal carcinoma. In this clinical trail, we will compare the diagnostic value of 68Ga-C1 PET/CT and 18F-FDG PET/CT in Chinese patients with indeterminate renal masses or confirmed clear cell renal cell carcinoma.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
200
Inclusion Criteria
  1. Signed written informed consent;
  2. Age ≥18;
  3. Patients with confirmed or suspected clear cell renal cell carcinoma;
  4. Expected survival ≥6 months.
Exclusion Criteria
  1. Renal mass is known to be a metastasis of another primary tumor;
  2. Have other malignancies that require treatment;
  3. Have received chemotherapy, radiotherapy, or immunotherapy within 4 weeks;
  4. Renal insufficiency with glomerular filtration rate (GFR) ≤ 60 mL/min/1.73 m²;
  5. Pregnant and lactating women or female patients plan to become pregnant within 6 months;
  6. Uncontrolled psychiatric disorders;
  7. Vulnerable population (e.g., being in detention) or have a serious non-malignant disease (e.g., infectious disease, autoimmune disease, or metabolic disease).

Study & Design

Study Type
INTERVENTIONAL
Study Design
SINGLE_GROUP
Arm && Interventions
GroupInterventionDescription
68Ga-C168Ga-C1Subjects with suspected or confirmed clear cell renal cell carcinoma will receive an intravenous injection of 68Ga-C1 followed by PET imaging. The subjects will also receive a whole-body 18F-FDG PET/CT scan within a one-week period.
Primary Outcome Measures
NameTimeMethod
The diagnostic efficacy of 68Ga-C1 PET/CT in the evaluation of malignant tumors1 year

Compare the number of lesions detected by 68Ga-C1 and 18F-FDG PET/CT, based on the pathology or clinical follow-up as gold standard.

The diagnostic efficacy of 68Ga-C1 PET/CT in the evaluation of clear cell renal cell carcinoma1 year

Compare the standardized Uptake Value (SUV) of lesions on 68Ga-C1 and 18F-FDG PET/CT

Secondary Outcome Measures
NameTimeMethod
Quantitative evaluation of 68Ga-C11 year

Evaluation of quantitative parameters of 68Ga-C1, such as time-activity curve.

The dosimetry of 68Ga-C11 year

Research on the dose distribution of 68Ga-C1 in healthy volunteers and cancer patients by 1-hour dynamic PET/CT acquisition and analyze by the dosimetry software

Correlation with pathological expression1 year

Analyze CAIX expression at the imaging level in combination with CAIX expression in pathological specimens

Trial Locations

Locations (1)

Peking University First Hospital

🇨🇳

Beijing, Beijing, China

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