[18F] Fluorocholine FCH Positron Emission Tomography (PET)/Computed Tomography (CT) for Detection of Prostate Cancer Lymph Nodes Metastases (PROPET)
Primary Purpose
Prostate Cancer
Status
Unknown status
Phase
Not Applicable
Locations
Denmark
Study Type
Interventional
Intervention
[18F] Fluorocholine PET/CT
Sponsored by
About this trial
This is an interventional diagnostic trial for Prostate Cancer focused on measuring Prostate cancer, [18F] Fluorocholine PET/CT, FCH, lymph node metastasis, staging, sensitivity, specificity, PROPET
Eligibility Criteria
Inclusion Criteria:
- Patients with a biopsy confirmed prostate cancer who awaits curative treatment and have
- An elevated level of prostate-specific antigen PSA>10 ng/mL (nanogram per milliliter) or/and
- A Gleason score > 6 or/and
- A TNM staging of T3
Exclusion Criteria:
- Patients who withdraw their informed consent.
- Patients who have a bone scan indicates metastatic prostate cancer.
- Patients who have a TNM stage is T4
In the case we detect a patient having an obvious other major illness e.g. lung cancer, the patient is referred to relevant treatment. Depending on the illness the might be excluded from the study.
Sites / Locations
- Department of Urology, Odense University HospitalRecruiting
Outcomes
Primary Outcome Measures
The primary target variable "metastasizes to regional lymph nodes" (yes/no) will be used to estimate the diagnostic usefulness of FCH PET/CT in terms of sensitivity, specificity, positive and negative predictive values.
Secondary Outcome Measures
Full Information
NCT ID
NCT00670527
First Posted
April 29, 2008
Last Updated
October 5, 2012
Sponsor
Odense University Hospital
Collaborators
University of Southern Denmark
1. Study Identification
Unique Protocol Identification Number
NCT00670527
Brief Title
[18F] Fluorocholine FCH Positron Emission Tomography (PET)/Computed Tomography (CT) for Detection of Prostate Cancer Lymph Nodes Metastases
Acronym
PROPET
Official Title
Evaluation of [18F] Fluorocholine PET/CT for Detection of Regional Lymph Node Metastases From Prostate Cancer
Study Type
Interventional
2. Study Status
Record Verification Date
October 2012
Overall Recruitment Status
Unknown status
Study Start Date
January 2008 (undefined)
Primary Completion Date
February 2013 (Anticipated)
Study Completion Date
April 2013 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
Odense University Hospital
Collaborators
University of Southern Denmark
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The objective of this trial is to assess the value of 18F-choline PET/CT for the detection of regional lymph node metastases from prostate cancer. In addition, the investigators want to evaluate whether 18F-choline PET/CT can replace lymphadenectomy for the staging of prostate cancer.
Detailed Description
The purpose of this prospective trail is to improve the staging of patients with prostate cancer. The investigators focus on the group of patients with a newly diagnosed prostate cancer, and specifically the ones who have an intermediate and high risk of disseminated prostate cancer.
The aim is to improve staging by replacing the traditional invasive method, the lymphadenectomy, which has a rather low sensitivity by a non-invasive method, 18F-choline PET/CT which has a presumably superior sensitivity.
The treatment of patients with prostate cancer relies on the stage of the disease. Patients with disseminated prostate cancer are incurable and are treated with palliatively. In contrast, patients with localized prostate cancer are offered curative therapy. Hence, the stage of prostate cancer is crucial for the choice of treatment.
The potential benefits are
The patients avoid the surgical trauma including complications and convalescents period.
The accuracy of the prostate cancer staging is improved, the potential of which is better survival.
The patients are 18F-choline PET/CT scanned prior to their lymphadenectomy, the results of the 18F-choline PET/CT are blinded for the surgeon. The endpoint of the trail is the comparison of 18F-choline PET/CT and the histopathological investigation of the regional lymph nodes of prostate.
Assuming a prevalence of metastasised prostate cancer of 20% and a true (unknown) sensitivity of FCH PET/CT of 95%, 205 patients are sufficient to show that the sensitivity of the FCH PET/CT is greater than 80% with a power of 80% at significance level 5%. The size of the confidence interval for specificity of FCH PET/CT is expected to become reasonable small. In opposition to lymphadenectomy, FCH PET/CT results may point to metastases in neighbouring regions which gives an additional benefit to FCH PET/CT justifying a test level for sensitivity of 80%."
Accordingly 205 patients will be included over 2½ years. The first patients have been included in January 2008. Interim analyses will be done after 25, 50 and 100 patients.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Prostate cancer, [18F] Fluorocholine PET/CT, FCH, lymph node metastasis, staging, sensitivity, specificity, PROPET
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
ParticipantCare ProviderInvestigator
Allocation
Non-Randomized
Enrollment
205 (Anticipated)
8. Arms, Groups, and Interventions
Intervention Type
Procedure
Intervention Name(s)
[18F] Fluorocholine PET/CT
Intervention Description
The patients fast 6 hours before the [18F]Fluorocholine PET/CT scan. [18F]Fluorocholine will be used as tracer with a dosage of 4 MBq per kg bodyweight. PET/CT imaging will be performed after 15 and 60 after the intravenous injection of the tracer. The patient will receive 2 full body FCH PET/CT. The CT scan is with contrast.
The radiation exposure from the CT scan is 9 mSv and from the PET scan it is 3 mSv, giving a total of 12 mSv, which equals 4 times the yearly background radiation in Denmark.
Primary Outcome Measure Information:
Title
The primary target variable "metastasizes to regional lymph nodes" (yes/no) will be used to estimate the diagnostic usefulness of FCH PET/CT in terms of sensitivity, specificity, positive and negative predictive values.
Time Frame
The [18F] Fluorocholin PET/CT and the lymphadenectomi is done within 1 month
10. Eligibility
Sex
Male
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Patients with a biopsy confirmed prostate cancer who awaits curative treatment and have
An elevated level of prostate-specific antigen PSA>10 ng/mL (nanogram per milliliter) or/and
A Gleason score > 6 or/and
A TNM staging of T3
Exclusion Criteria:
Patients who withdraw their informed consent.
Patients who have a bone scan indicates metastatic prostate cancer.
Patients who have a TNM stage is T4
In the case we detect a patient having an obvious other major illness e.g. lung cancer, the patient is referred to relevant treatment. Depending on the illness the might be excluded from the study.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Mads Hvid Poulsen, MD
Email
Mads.Poulsen@ouh.regionsyddanmark.dk
First Name & Middle Initial & Last Name or Official Title & Degree
Steen Walter, MD, DMSci, Professor
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Mads Hvid Poulsen, MD
Organizational Affiliation
Department of Urology, Odense University Hospital, Denmark
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Ulla Geertsen, MD, Head of Department
Organizational Affiliation
Department of Urology, Odense University Hospital, Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Niels Svolgaard, MD, Senior Physician
Organizational Affiliation
Department of Urology, Odense University Hospital, Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Steen Walter, MD, DMSci, Professor
Organizational Affiliation
Department of Urology, Odense University Hospital, Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Kirsten Bouchelouche, MD, DMSci
Organizational Affiliation
Odense University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mette Høilund-Carlsen, Head Technician
Organizational Affiliation
Odense University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Henrik Petersen, MD, Senior Physician
Organizational Affiliation
Odense University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Mattias Ögren, Radiochemist, PhD
Organizational Affiliation
Odense University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Poul F Høilund-Carlsen, MD, DMSci, Professor
Organizational Affiliation
Department of Nuclear Medicine, Odense University Hospital, Demnark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Oke Gerke, Post-Doc, PhD
Organizational Affiliation
University of Southern Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Werner Vach, PhD, Professor
Organizational Affiliation
University of Southern Denmark
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Birgitte Svolgaard, MD, Senior Physician
Organizational Affiliation
Odense University Hospital
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Niels Marcussen, MD, DMSci, Professor
Organizational Affiliation
Odense University Hospital
Official's Role
Study Chair
Facility Information:
Facility Name
Department of Urology, Odense University Hospital
City
Odense
ZIP/Postal Code
5000
Country
Denmark
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Mads Hvid Poulsen, MD
Email
Mads.Poulsen@ouh.regionsyddanmark.dk
First Name & Middle Initial & Last Name & Degree
Steen Walter
12. IPD Sharing Statement
Citations:
PubMed Identifier
22520686
Citation
Poulsen MH, Bouchelouche K, Hoilund-Carlsen PF, Petersen H, Gerke O, Steffansen SI, Marcussen N, Svolgaard N, Vach W, Geertsen U, Walter S. [18F]fluoromethylcholine (FCH) positron emission tomography/computed tomography (PET/CT) for lymph node staging of prostate cancer: a prospective study of 210 patients. BJU Int. 2012 Dec;110(11):1666-71. doi: 10.1111/j.1464-410X.2012.11150.x. Epub 2012 Apr 23.
Results Reference
derived
Learn more about this trial
[18F] Fluorocholine FCH Positron Emission Tomography (PET)/Computed Tomography (CT) for Detection of Prostate Cancer Lymph Nodes Metastases
We'll reach out to this number within 24 hrs