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Fiducial Localization and Individualized Radiotherapy -Prostate Cancer (FLIP)

Primary Purpose

Prostate Cancer

Status
Active
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Transrectal APT Device or Transperineal Device will be used
TRUS probe
Sponsored by
University Health Network, Toronto
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Cancer focused on measuring prostate cancer, individualized radiotherapy, fiducial markers, MRI, ultrasound, High-Risk Localized Prostate Cancer

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)MaleDoes not accept healthy volunteers

Inclusion Criteria:

  1. ≥ 18 years old
  2. ECOG status ≤ 1
  3. High risk localized cancer planned for RT under FM guidance
  4. Gleason > 7, PSA > 20, Clinical stage ≥ T3
  5. patients(pts) must give written informed consent

Exclusion Criteria:

  1. pts > 136 kg or > 60 cm in girth
  2. Pts with pacemakers, cerebral aneurysm clips, shrapnel injury or devices not compatible with MRI.
  3. pts with severe claustrophobia
  4. pts with bleeding diathesis and anticoagulative therapy that cannot be ceased prior to needle procedures.
  5. Contraindications to endorectal probe, surgically absent rectum, severe hemorrhoids or previous colorectal surgery.
  6. Latex Allergy

Sites / Locations

  • University Health Network

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

MRI-guided FM

TRUS-guided FM

Arm Description

Outcomes

Primary Outcome Measures

To compare the performance of MRI and TRUS images in guiding the insertion of a fiducial marker within the Gross Target Volume (GTV)

Secondary Outcome Measures

To measure the needle targeting accuracy of the MRI-guided technique.
To validate the accuracy of identifying the GTV on MRI.
To evaluate MRI methods for the characterization of tissue oxygenation.
To evaluate the effect of neoadjuvant hormone therapy on tissue oxygenation.

Full Information

First Posted
November 11, 2008
Last Updated
May 7, 2023
Sponsor
University Health Network, Toronto
Collaborators
Princess Margaret Hospital, Canada
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1. Study Identification

Unique Protocol Identification Number
NCT00789607
Brief Title
Fiducial Localization and Individualized Radiotherapy -Prostate Cancer
Acronym
FLIP
Official Title
Fiducial Localization and Individualized Radiotherapy in Prostate Cancer (FLIP)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2023
Overall Recruitment Status
Active, not recruiting
Study Start Date
June 2008 (undefined)
Primary Completion Date
June 2017 (Actual)
Study Completion Date
October 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
University Health Network, Toronto
Collaborators
Princess Margaret Hospital, Canada

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This purpose of this study is designed to compare two types of images; magnetic resonance imaging (MRI) and Trans-Rectal Ultrasound (TRUS) to see which one performs more accurately for the image-guided insertion of Fiducial Markers(FMs) within the tumour. Though effective for guiding FM placement at the poles of the prostate gland due to excellent visualization of the prostatic boundaries, TRUS may not be ideally suited for marking the GTV. Conventional TRUS is neither sufficiently sensitive nor specific for accurate visualization of intra-prostatic tumor. A new interventional MRI technique enables needle guidance to the gross tumour Volume (GTV) for FM placement. It is of particular importance that both techniques be evaluated to enable which one is more effective so that it can be implemented in the designs of future trials involving dose-escalation to prostate.
Detailed Description
The success of dose escalation strategies in prostate cancer over the last decade has relied on high accuracy in target delineation, localization and radiation delivery. Improved biochemical control with acceptable levels of toxicity (specifically rectal) has been achieved by stringently monitoring the location of the prostate during the course of radiation treatment. Studies in the early 1990's demonstrated that daily bony alignment was a poor surrogate for prostate gland location. Since then, various strategies have been devised to localize the prostate precisely during treatment. Of these, Transrectal Ultrasound (TRUS)-guided gold fiducial marker (FM) insertion and x-ray imaging of markers has been a broadly successful approach. TRUS guidance has been used for fiducial marker insertion within the prostate since 1985 in various centers throughout the world and has also been a standard practice in PMH since 1997 in men undergoing radical external beam radiotherapy. A retrospective comparative study of 106 patients evaluating the relative accuracy of endorectal MRI and TRUS in detecting the location of tumor reported an improved performance of endorectal MRI especially in the base and midgland regions. Over the last few years, mounting experience in the interpretation of prostate MRI, and addition of physiologic imaging sequences has further improved the performance of MRI in detecting and localizing the GTV.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
prostate cancer, individualized radiotherapy, fiducial markers, MRI, ultrasound, High-Risk Localized Prostate Cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
17 (Actual)

8. Arms, Groups, and Interventions

Arm Title
MRI-guided FM
Arm Type
Active Comparator
Arm Title
TRUS-guided FM
Arm Type
Active Comparator
Intervention Type
Device
Intervention Name(s)
Transrectal APT Device or Transperineal Device will be used
Intervention Description
Both are imaging probe devices that is inserted under local anesthetic, in the rectum using lubricant, positioning against the prostate gland, and attached to the table. This is done at baseline (Day 0) under local anesthetic with the patient in partial dorsal lithotomy position
Intervention Type
Device
Intervention Name(s)
TRUS probe
Intervention Description
Patient is given local anesthetic transrectally to the prostate base and the probe is inserted with patient in the lateral decubitus position.
Primary Outcome Measure Information:
Title
To compare the performance of MRI and TRUS images in guiding the insertion of a fiducial marker within the Gross Target Volume (GTV)
Time Frame
5 years
Secondary Outcome Measure Information:
Title
To measure the needle targeting accuracy of the MRI-guided technique.
Time Frame
5 years
Title
To validate the accuracy of identifying the GTV on MRI.
Time Frame
5 years
Title
To evaluate MRI methods for the characterization of tissue oxygenation.
Time Frame
5 years
Title
To evaluate the effect of neoadjuvant hormone therapy on tissue oxygenation.
Time Frame
5 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: ≥ 18 years old ECOG status ≤ 1 High risk localized cancer planned for RT under FM guidance Gleason > 7, PSA > 20, Clinical stage ≥ T3 patients(pts) must give written informed consent Exclusion Criteria: pts > 136 kg or > 60 cm in girth Pts with pacemakers, cerebral aneurysm clips, shrapnel injury or devices not compatible with MRI. pts with severe claustrophobia pts with bleeding diathesis and anticoagulative therapy that cannot be ceased prior to needle procedures. Contraindications to endorectal probe, surgically absent rectum, severe hemorrhoids or previous colorectal surgery. Latex Allergy
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Peter Chung, MD
Organizational Affiliation
University Health Network, Toronto
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Health Network
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M5G 2M9
Country
Canada

12. IPD Sharing Statement

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Fiducial Localization and Individualized Radiotherapy -Prostate Cancer

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