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Molecular PET/MR Imaging in Vivo Validation of Biomarker for Human Prostate Cancer

Molecular PET/MR Imaging in Vivo Validation of Biomarker for Human Prostate Cancer

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03451812
Acronym
PCAPETMR
Enrollment
120
Registered
2018-03-02
Start date
2017-01-01
Completion date
2019-12-31
Last updated
2019-08-08

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Prostate Adenocarcinoma

Keywords

prostate cancer, metabolomics, molecular imaging, PET, MRI, 11C-choline tracer

Brief summary

Primary objective: To correlate the blood/urine metabolomic biomarkers with PET/MR imaging. Secondary objectives: 1. To evaluate the sensitivity and specificity of the PET/MR in diagnosis of prostate cancer. 2. To examine the diagnostic performance among subgroups of defined high-risk and low-risk subjects. 3. To interrogate the metabolomic alterations with the molecular PET/MR to develop workable panel biomarkers.

Detailed description

According to 2015 National Comprehensive Cancer Network (NCCN) guideline, medical imaging plays important roles for detection and staging for PCa, in addition to blood or urine biomarkers. Although there are a number of very different diagnostic imaging methods, e.g. transrectal ultrasound (TRUS), computed tomography (CT), magnetic resonance (MR) imaging and spectroscopy, or 18F-FDG positron emission tomography (PET), none of these have gained a dominant role as the optimum method for all clinical scenarios.The recently added armamentarium, PET/MR, might improve diagnosis in this regard. Therefore, we conduct this trial to identify the ability of \[11C\]Choline PET/MR to evaluate the patients with prostate cancer, especially under the circumstance of elevated PSA level.

Interventions

None listed

Sponsors

Chang Gung Memorial Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_ONLY
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
MALE
Age
40 Years to 85 Years
Healthy volunteers
No

Inclusion criteria

* Males * 40-85 years of age * Patients with a biopsy-proven or clinically highly suspected prostate adenocarcinoma, or benign prostatic hyperplasia * Able to tolerate \[11C\]Choline PET scan and MRI scan * Written informed consent from the patient

Exclusion criteria

* Acute prostatitis or non-urologic bacterial infection requiring medical treatment within the last 3 months. * History of AIDS in the period prior to the screening.3 * Contraindications to \[11C\]Choline PET/MR scans 1. Surgical implants including pacemaker implants, cochlear implants, dentures held in place by magnets imbedded in the gums and aneurysm clips except those inserted at CGMH 2. Metallic prosthesis of the hip or pelvic region 3. Renal function impairment with estimated glomerular filtration rate (eGFR) \< 30 ml/min/1.73 m2 4. Claustrophobia 5. Medical drugs with choline 6. Previous allergy to carbon-labeled radionuclide * Active other malignancy within the last 2 years * Subject which in the opinion of the investigator preclude participation for scientific reasons, for reasons of compliance, or for reasons of the subject's safety. * Prisoners or patients with mental illness

Design outcomes

Primary

MeasureTime frameDescription
Diagnostic Accuracy1 yearsensitivity, specificity, accuracy

Countries

Taiwan

Contacts

Primary ContactGigin Lin, MD, PhD
giginlin@cgmh.org.tw886-3281200

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026