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Preoperative Staging and Dose Escalated Radiotherapy of Prostate Carcinoma With PET and MRI (Flucipro)

Primary Purpose

Prostate Carcinoma

Status
Completed
Phase
Phase 2
Locations
Finland
Study Type
Interventional
Intervention
PET/CT, PET/MRI, mpMRI
Sponsored by
Turku University Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostate Carcinoma focused on measuring FACBC, PET/CT, PET/MRI, Radical prostatectomy, Radiotherapy

Eligibility Criteria

50 Years - 85 Years (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  • Age: 50 to 85 years old
  • Language spoken: Finnish or Swedish
  • Diagnosis: Histologically confirmed adenocarcinoma of prostate
  • Adequate histological sampling consisting of at least 3 biopsy samples from each lobe
  • No previous surgical, radiation or endocrine treatment for prostate carcinoma
  • Clinical stage T1c-T3aN0 based on transrectal ultrasound
  • Serum creatinine ≤ 1,5 x upper limit of normal (ULN)
  • Patient agrees to undergo either surgery or external radiotherapy
  • Mental status: Patients must be able to understand the meaning of the study
  • Informed consent: The patient must sign the appropriate Ethical Committee (EC) approved informed consent documents in the presence of the designated staff

Exclusion Criteria:

  • Prior medical history: Patient must have no history of serious cardiovascular, liver or kidney disease
  • Infections: Patient must not have an uncontrolled serious infection
  • No contraindications for MRI (cardiac pacemaker, intracranial clips etc)
  • Patient preference for active surveillance as a method of prostate cancer management

Sites / Locations

  • Turku University Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Multimodality imaging

Arm Description

PET/CT, PET/MRI, mpMRI

Outcomes

Primary Outcome Measures

Diagnostic accuracy of hybrid PET/MRI with FACBC
By comparing tracer uptake and imaging findings at MRI in each sextant with macroslices obtained at radical prostatectomy sensitivity, specificity, positive and negative predictive value and accuracy will be calculated

Secondary Outcome Measures

Biochemical relapse free survival (bRFS)
By sequential measurements of serum PSA bRFS will be determined in patients having biologically guided radiotherapy (BGRT) plans. BGRT is performed with dose painting of hot spots at PET/MRI

Full Information

First Posted
November 29, 2013
Last Updated
October 20, 2016
Sponsor
Turku University Hospital
Collaborators
GE Healthcare, Blue Earth Diagnostics
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1. Study Identification

Unique Protocol Identification Number
NCT02002455
Brief Title
Preoperative Staging and Dose Escalated Radiotherapy of Prostate Carcinoma With PET and MRI
Acronym
Flucipro
Official Title
Preoperative Staging and Dose Escalated Radiotherapy of Prostate Carcinoma
Study Type
Interventional

2. Study Status

Record Verification Date
October 2016
Overall Recruitment Status
Completed
Study Start Date
December 2013 (undefined)
Primary Completion Date
May 2016 (Actual)
Study Completion Date
June 2016 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Turku University Hospital
Collaborators
GE Healthcare, Blue Earth Diagnostics

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
Prostate cancer (PCa) is currently the most common neoplastic disease among men in well-developed countries with 350 000 new cases diagnosed annually in Europe and 4 800 in Finland. Due to widespread use of serum prostate specific antigen (PSA) in asymptomatic men, most patients present initially with localized disease. Radical prostatectomy, radiotherapy (RT) and active surveillance are the most common management options for patients with localized PCa. Proper preoperative staging for patients with adverse features on biopsy who are candidates for radical prostatectomy is urgently needed. For elderly men external beam RT is the preferred modality which can be safely performed utilizing modern techniques such as intensity modulated and image guided radiotherapy (IMRT and IGRT). Since randomized studies suggest a dose response effect beyond 78-80 Gy newer techniques aim at dose escalation provided that toxicity can be controlled. Therefore, ultra high dose IMRT/IGRT requires visualization of intracapsular disease which will receive the highest dose. Taken together, the use of accurate anatomical and functional imaging modalities are essential for planning both nerve sparing radical prostatectomy and ultra high dose IMRT/IGRT Fluorine-18 labeled L-leucine analogue 1-amino-3-fluorocyclobutane-1-carboxylic acid (FACBC) has shown to preferentially accumulate in PCa and its nodal metastases. By assisting in localization of intraprostatic and pelvic disease FACBC with hybrid positron emission tomography/computed tomography (PET/CT) or magnetic resonance imaging (PET/MRI) has potential to improve selection of patients for robot-assisted radical prostatectomy and IMRT/IGRT. Anatomical MRI at 1.5 Tesla (T) compared with transrectal ultrasound has demonstrated a higher sensitivity for tumor detection but almost the same specificity, stressing the need for additional metabolic MRI. Advanced application of MRI such as proton magnetic resonance spectroscopy (1H MRS), diffusion weighted imaging (DWI) and dynamic contrast enhanced imaging (DCE-MRI) are increasingly being used for detection and characterization of PCa. The use of 3T scanners and multiparametric MRI (mpMRI), consisting of anatomical MRI, DWI, 1H MRS and DCE-MRI, demonstrated very promising result for staging and detection of PCa.
Detailed Description
Specific aims of the current study are as follows: i) To determine the sensitivity, specificity and accuracy of multiparametric 3T MRI, (anatomical MRI, DCE-MRI, DWI and 1H MRS) combined with FACBC PET/CT and PET/MRI in correlation with systematic biopsy and whole mount prostatectomy specimens. ii) To asses the applicability of multiparametric 3T MRI combined with FACBC-PET/CT and PET/MRI for detection of cancer aggressiveness based on Gleason score and PSA. iii) To develop quantitative and qualitative methods for evaluation of FACBC PET/MRI iv) To develop and validate an imaging protocol which will become the standard protocol for prostate imaging both for surgical and radiotherapy patients at Turku PET Centre using hybrid PET/MRI

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Carcinoma
Keywords
FACBC, PET/CT, PET/MRI, Radical prostatectomy, Radiotherapy

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
26 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Multimodality imaging
Arm Type
Experimental
Arm Description
PET/CT, PET/MRI, mpMRI
Intervention Type
Device
Intervention Name(s)
PET/CT, PET/MRI, mpMRI
Intervention Description
FACBC dose 370 megabecquerel (MBq)
Primary Outcome Measure Information:
Title
Diagnostic accuracy of hybrid PET/MRI with FACBC
Description
By comparing tracer uptake and imaging findings at MRI in each sextant with macroslices obtained at radical prostatectomy sensitivity, specificity, positive and negative predictive value and accuracy will be calculated
Time Frame
1 years
Secondary Outcome Measure Information:
Title
Biochemical relapse free survival (bRFS)
Description
By sequential measurements of serum PSA bRFS will be determined in patients having biologically guided radiotherapy (BGRT) plans. BGRT is performed with dose painting of hot spots at PET/MRI
Time Frame
5 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
50 Years
Maximum Age & Unit of Time
85 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age: 50 to 85 years old Language spoken: Finnish or Swedish Diagnosis: Histologically confirmed adenocarcinoma of prostate Adequate histological sampling consisting of at least 3 biopsy samples from each lobe No previous surgical, radiation or endocrine treatment for prostate carcinoma Clinical stage T1c-T3aN0 based on transrectal ultrasound Serum creatinine ≤ 1,5 x upper limit of normal (ULN) Patient agrees to undergo either surgery or external radiotherapy Mental status: Patients must be able to understand the meaning of the study Informed consent: The patient must sign the appropriate Ethical Committee (EC) approved informed consent documents in the presence of the designated staff Exclusion Criteria: Prior medical history: Patient must have no history of serious cardiovascular, liver or kidney disease Infections: Patient must not have an uncontrolled serious infection No contraindications for MRI (cardiac pacemaker, intracranial clips etc) Patient preference for active surveillance as a method of prostate cancer management
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Heikki Minn, Professor
Organizational Affiliation
Turku University Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Turku University Hospital
City
Turku
ZIP/Postal Code
20521
Country
Finland

12. IPD Sharing Statement

Plan to Share IPD
Undecided
Citations:
PubMed Identifier
29147764
Citation
Jambor I, Kuisma A, Kahkonen E, Kemppainen J, Merisaari H, Eskola O, Teuho J, Perez IM, Pesola M, Aronen HJ, Bostrom PJ, Taimen P, Minn H. Prospective evaluation of 18F-FACBC PET/CT and PET/MRI versus multiparametric MRI in intermediate- to high-risk prostate cancer patients (FLUCIPRO trial). Eur J Nucl Med Mol Imaging. 2018 Mar;45(3):355-364. doi: 10.1007/s00259-017-3875-1. Epub 2017 Nov 16.
Results Reference
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Preoperative Staging and Dose Escalated Radiotherapy of Prostate Carcinoma With PET and MRI

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