99mTc-P137 SPECT/CT in Prostate Cancer

Xi'an Jiaotong University

Status: Enrolling

Conditions: Prostate Cancer

Treatments: Diagnostic Test: SPECT/CT imaging with 99mTc-P137 nuclide probe

Study type: Interventional

Funder types: Other

Identifiers

NCT05672485

XJTU1AF2022LSK-356

Details and patient eligibility

About

Purpose: This study will take prostate specific membrane antigen (PSMA) as the targeting of radionuclide labeled molecular probe to explore the diagnostic efficacy of 99mTc-P137 radioactive probe in prostate cancer. Combining with SPECT/CT to optimize the imaging, image analysis and clinical diagnosis process of 99mTc-P137 probe, the aim of the study is to provide new methods and new means for the early detection, early diagnosis, accurate tumor staging, treatment decision and prognosis judgment of malignant tumor, and will provide scientific and clinical basis for the precise diagnosis and treatment of prostate cancer.

Research objectives: To investigate the clinical translational application value of 99mTc-P137 molecular probe in accurate detection of prostate cancer lesions.

Research design: A prospective study design will be used in this study. Patients meeting the inclusion criteria of this study will be analyzed with 99mTc-P137 SPECT/CT imaging. To evaluate the diagnostic and prognostic value of 99mTc-P137 nuclear medicine imaging in accurate detection of prostate cancer lesions, clinical surgical specimens and pathological diagnosis will be used as the gold standard.

Study the population Indications: For patients with suspected prostate cancer who plan to undergo surgical resection or puncture biopsy after various examinations, the final pathological results can be obtained.

Enrollment: 40 estimated patients

Sex: Male

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients age 18 or above;
• highly suspicious for prostate cancer patients: 1) Serum PSA is significantly changed compared with before (PSA<4.0ng/mL with annual change >0.35ng/mL; or PSA > 4.0ng/mL with annual change > 0.75ng/mL); 2) First or second degree relatives have a history of prostate cancer; 3) Nuclear magnetic PI-RADS score ≥3 points;
• the prostate biopsy or surgical pathology is diagnosed with prostate cancer;
• available to provide clinical laboratory results (blood routine, biochemical and serum PSA) within one month before this study; At least two imaging examinations including CT, MRI, nuclear medicine (PET/CT or SPECT/CT), ultrasound and other imaging techniques;
• Can complete the inspection autonomously;
• voluntary and signed informed consent.

Exclusion criteria

• there are other malignant tumor history;
• severe damage of liver and kidney function;
• may not be able to obtain pathology or long-term follow-up results;
• don't have access to relevant reference image data and clinical data;
• difficult to cooperate.

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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40 participants in 1 patient group

Patients diagnosed with prostate cancer

Experimental group

Treatment:

Diagnostic Test: SPECT/CT imaging with 99mTc-P137 nuclide probe