Choline-PET: Exploratory Study Assessing the Potential Role of F-choline PET Imaging in New and Emerging Indications

Sponsor
Centre hospitalier de l'Université de Montréal (CHUM) (Other)
Overall Status
Active, not recruiting
CT.gov ID
NCT04999215
Collaborator
(none)
500
1
1
121
4.1

Study Details

Study Description

Brief Summary

Choline is an important building block of phospholipids in cell membranes. Certain cancers and medical conditions are known to demonstrate increased absorption and incorporation of choline into their cell membranes. 18-F-fluorocholine (F-choline) and 11-C-choline (C-choline) are diagnostic positron emission tomography (PET) radiotracers that can be used to image, in vivo, the metabolism of choline. Both tracers have been extensively studied in prostate cancer and C-choline has obtained US FDA approval for the investigation of recurrent prostate cancer. F-choline is currently not approved for clinical use by the FDA or Health Canada, but it offers many advantages over C-choline due to its better physical characteristics (mainly due to its positron range, shorter and longer half-life). In recent years, reports have started to emerge on broader potential applications of choline PET imaging, particularly for imaging parathyroid adenomas, certain cervical cancers and certain liver cancers.

The main objective is to discover and explore potential new and emerging indications in which F-choline could play a role and provide clinically relevant information.

Secondary objectives are 1) To assess the safety of F-choline PET imaging using F-choline produced at the CRCHUM; 2) assess changes in patient/disease management following F-choline PET imaging.

Researchers hypothesize that F-choline will provide useful and incremental clinical information in a variety of conditions, and outperform the "standard" workup in numerous conditions.

F-Choline PET exams will be performed on hybrid PET/CT scanners according to standard procedures. These examinations could be repeated at the discretion of the treating physician (up to a maximum of 4 exams per year) if the treating physician and the research team deem this could provide additional clinically useful information (for example, by helping to assess response to newly started therapy).

The results will be provided to the attending physician and any new knowledge could lead to a change in treatment or an investigation of the condition that prompted enrollment in the study.

Condition or Disease Intervention/Treatment Phase
  • Drug: F-choline intravenous injection
Phase 3

Study Design

Study Type:
Interventional
Anticipated Enrollment :
500 participants
Allocation:
N/A
Intervention Model:
Single Group Assignment
Masking:
None (Open Label)
Primary Purpose:
Diagnostic
Official Title:
Choline-PET: Exploratory Study Assessing the Potential Role of F-choline PET Imaging in New and Emerging Indications
Actual Study Start Date :
Jul 1, 2022
Anticipated Primary Completion Date :
Jul 1, 2032
Anticipated Study Completion Date :
Aug 1, 2032

Arms and Interventions

Arm Intervention/Treatment
Experimental: Main arm

F-choline intravenous injection

Drug: F-choline intravenous injection
Participants will receive one injection of F-choline before undergoing hybrid PET/CT imaging per standard procedures. F-choline PET examinations may be repeated, if this judged to be in the patient's best interest by his referring physician and the study staff, up to a maximum 4 examinations per year.

Outcome Measures

Primary Outcome Measures

  1. Diagnostic performance (sensitivity and specificity) of F-choline PET/CT [3 months]

    "Gold-standard" will be a composite of other imaging modalities, pathological data when available, and clinical follow-up.

  2. Adverse reaction to the F-choline injection [24 hours]

    Absence or presence of adverse reactions related to F-choline injection (yes or no)

Secondary Outcome Measures

  1. Change in management following F-choline PET/CT [3 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
Inclusion Criteria:
  • Any patient with a known or suspected condition in which F-choline PET imaging might provide clinically useful information.
Exclusion Criteria:
  • Pregnancy

  • Breastfeeding woman, unwilling to discontinue breastfeeding for 48 hours

  • Known allergy to F-choline or any excipients

  • Pediatric patient (< 18 years old)

Contacts and Locations

Locations

Site City State Country Postal Code
1 Centre Hospitalier de l'université de Montréal Montréal Quebec Canada H2X 0C1

Sponsors and Collaborators

  • Centre hospitalier de l'Université de Montréal (CHUM)

Investigators

  • Principal Investigator: Daniel Juneau, MD, Centre hospitalier de l'Université de Montréal (CHUM)

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Centre hospitalier de l'Université de Montréal (CHUM)
ClinicalTrials.gov Identifier:
NCT04999215
Other Study ID Numbers:
  • 2021-9489
First Posted:
Aug 10, 2021
Last Update Posted:
Jul 28, 2022
Last Verified:
Jul 1, 2022
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Centre hospitalier de l'Université de Montréal (CHUM)
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 28, 2022