11C- and 18F-Choline PET/MR Imaging for Prostate Cancer

University of California San Francisco (UCSF)

Status and phase: Completed; Phase 2

Conditions: Prostate Cancer

Treatments: Procedure: Positron Emission Tomography (PET) / Magnetic Resonance Imaging (MRI); Drug: Carbon C 11 Choline; Drug: Fluorine F 18 Choline

Study type: Interventional

Funder types: Other; NIH

Identifiers

NCT02397408

NCI-2015-00731 (Registry Identifier)

R01CA148708 (U.S. NIH Grant/Contract)

145511

Details and patient eligibility

About

This phase II trial studies how well 11C-choline (carbon C 11 choline) and 18F-choline (fluorine F 18 choline) positron emission tomography/magnetic resonance (PET/MR) imaging works in diagnosing patients with unfavorable intermediate to high-risk prostate cancer. Diagnostic procedures, such as 11C- and 18F-choline PET/MR may help find and diagnose prostate cancer and find out how far the disease has spread.

Full description

PRIMARY OBJECTIVES:

I. To assess the ability of 11C- and 18F-choline PET/MR to detect and localize prostate cancer within the prostate gland.

SECONDARY OBJECTIVES:

I. To assess the ability of 11C- and 18F-choline PET/MR to detect the specific location of metastatic prostate cancer within pelvic lymph node regions in patients undergoing radical prostatectomy and extended pelvic lymph node dissection.

II. To assess the comparative performance of 11C- and 18F-choline PET/MR to already available imaging scans (bone scan, sodium fluoride positron emission tomography/computed tomography [NaF PET/CT], multiparametric1H magnetic resonance imaging [MRI], and/or pelvic CT scans) for detecting and localization of disease within the prostate, lymph nodes, and distant metastatic sites.

III. To determine the temporal distribution of 11C- and 18F-choline radiotracer in patients. The tissue uptake, retention, and clearance will be determined.

EXPLORATORY OBJECTIVES:

I. To compare regions of uptake on the 11C- and 18F-choline PET/MR to that on the sentinel lymph node imaging scans in patients undergoing sentinel lymph node-guided extended pelvic lymph node dissection.

OUTLINE:

Patients undergo 11C- and 18F-choline whole-body PET/MR imaging. After completion of study treatment, patients are followed up for 3 hours

Enrollment: 18 patients

Sex: All

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Age: Patients must be >=18 years of age
• Diagnosis: Patients must have a diagnosis of prostate cancer by histologic verification and a hypoechoic lesion seen on ultrasound.
• Disease Status: Unfavorable intermediate to high-risk prostate cancer, per the Cancer of the Prostate Risk Assessment Score (CAPRA) (CAPRA 5-10)
• Karnofsky Performance Status >=70
• Metastatic workup: Whole Body Sodium Fluoride (NaF) PET/CT or 99mTc Bone Scan
• Planned to undergo radical prostatectomy and extended pelvic lymph node dissection
• Adequate bone marrow and organ function defined as follows:
• Adequate bone marrow function:
• Leukocytes >= 3,000/microliter (mcL)
• Absolute Neutrophil Count >= 1,500/mcL
• Platelets >= 100,000/mcL
• Adequate hepatic function:
• Total bilirubin - within normal institutional limits
• Aspartate aminotransferase (AST)/ serum glutamic-oxaloacetic transaminase (SGOT) <= 2.5 X institutional upper limit of normal
• Alanine aminotransferase (ALT)/serum glutamic-pyruvic transaminase (SGPT) <= 2.5 X institutional upper limit of normal
• Adequate renal function:
• Creatinine - within normal institutional limits OR
• Creatinine clearance >= 60 mL/min/ 1.73m2 for patients with creatinine levels above institutional normal
• Ability to understand a written informed consent document, and the willingness to sign it

Exclusion criteria

• Participation would significantly delay the scheduled standard of care therapy
• Karnofsky performance status of < 60
• Inadequate venous access
• Administered a radioisotope within 5 physical half lives prior to study enrollment
• Have a medical condition or other circumstances which, in the opinion of the investigator would significantly decrease the chances of obtaining reliable data, achieving the study objectives, or completing the study.

Trial design

Primary purpose: Diagnostic

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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18 participants in 1 patient group

Diagnostic 11C- and 18F-choline PET/MR imaging

Experimental group

Description:

Patients are given 370 megabecquerel (MBq) 11C-Choline (11C) intravenously and 3 MBq/kg 18F-Choline (18F) intravenously prior to a whole-body PET/MR imaging

Treatment:

Drug: Fluorine F 18 Choline

Drug: Carbon C 11 Choline

Procedure: Positron Emission Tomography (PET) / Magnetic Resonance Imaging (MRI)