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FOcal RECurrent Assessment and Salvage Treatment (FORECAST)

Primary Purpose

Progression of Prostate Cancer

Status
Unknown status
Phase
Phase 2
Locations
United Kingdom
Study Type
Interventional
Intervention
Whole Body MRI
Focal Salvage Therapy
MRI Targeted biopsies
Sponsored by
University College London Hospitals
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Progression of Prostate Cancer focused on measuring Biochemical Failure, Radiotherapy, Radiorecurrent Prostate Cancer, MRI Prostate, Whole Body MRI, Bone Scan, Choline PET, Focal Salvage Treatment, HIFU, Cryotherapy

Eligibility Criteria

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

Inclusion Criteria:

  1. Previous external beam radiotherapy with or without neo-adjuvant/adjuvant hormone therapy
  2. Biochemical failure as defined by the Phoenix criteria (PSA nadir + 2ng/ml)
  3. Men considering local salvage treatment for radio-recurrent disease
  4. Life expectancy of 5 years or more

Exclusion Criteria:

  1. Have taken any form of hormones (except 5-alpha reductase inhibitors) within the previous 6 months
  2. Unable to have MRI scan as defined by standard care practice
  3. Metallic implant likely to cause artefact and reduce scan quality
  4. PSA doubling time of 3 months or less
  5. PSA value 20ng/ml or greater
  6. Prior prostate biopsies following biochemical failure
  7. Any prior local intervention to the prostate (e.g., laser/electrical resection or incision, cryotherapy, HIFU, any other ablative modality, any other radiotherapy, any other prostate injection therapy for symptoms or cancer control)
  8. Unable to have general or regional anaesthesia
  9. Unable to give informed consent

Sites / Locations

  • Hampshire Hospitals NHS TrustRecruiting
  • University College London HospitalsRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm Type

Experimental

Experimental

Experimental

Arm Label

Whole body MRI

MRI Targeted Biopsies

Focal Salvage Therapy

Arm Description

Comparing the detection rate of metastases of whole body MRI compared to current standard of care tests - Choline PET and Bone scan.

Transperineal MRI-targeted biopsies and whole-gland transperineal prostate mapping biopsies

Focal salvage HIFU and cryotherapy of recurrent prostate cancer tumors only

Outcomes

Primary Outcome Measures

Accuracy of whole body MRI in identifying distant disease
Whole body MRI lesions suspicious of lymph node, visceral or bone metastases compared to standard care tests - Sensitivity, specificity, negative and positive predictive values of whole-body MRI to detect distant disease compared to standard care tests (isotope bone-scan, PET/CT-scan, with skeletal survey where appropriate) and/or pelvic lymphadenectomy and/or biopsy of distant areas in indeterminate cases

Secondary Outcome Measures

Can multiparametric MRI accurately detect localised recurrent prostate cancer
Imaging of Local Disease Transperineal multi-parametric MRI targeted biopsies compared to Template Prostate Mapping biopsies in the detection of UCL definition 2 clinically significant prostate cancer (Gleason >/=3+4 AND/OR Maximum Cancer Core Length >/=4mm in any one biopsy)

Full Information

First Posted
June 18, 2013
Last Updated
May 8, 2017
Sponsor
University College London Hospitals
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1. Study Identification

Unique Protocol Identification Number
NCT01883128
Brief Title
FOcal RECurrent Assessment and Salvage Treatment
Acronym
FORECAST
Official Title
An Evaluation of a Novel Imaging Based Complex Diagnostic and Therapeutic Pathway Intervention for Men Who Fail Radiotherapy for Prostate Cancer.
Study Type
Interventional

2. Study Status

Record Verification Date
May 2017
Overall Recruitment Status
Unknown status
Study Start Date
April 2014 (Actual)
Primary Completion Date
October 2019 (Anticipated)
Study Completion Date
October 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University College London Hospitals

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Radiotherapy is the commonest form of prostate cancer treatment in the UK. In one in four men, radiotherapy will fail to control the cancer. These men are offered hormonal treatment which has significant side effects. Few men are offered a further treatment such as surgery, HIFU or cryotherapy. Only half of these men are cancer free at 5 years. The investigators believe this is due to poor imaging tests such as CT and Bone scan that cannot accurately detect whether cancer has come back inside or outside of the prostate or both. Also radiotherapy damages tissue surrounding the prostate which affects tissue healing for example after surgery. Treating just the cancer in the prostate only (focal treatment) rather than the whole prostate may limit this damage and cause fewer side-effects. The investigators want to see if new imaging tests can better identify cancer that has spread outside of the prostate and areas of cancer inside the prostate. Our new tests are whole-body MRI (for distant disease) and MRI guided biopsies (MRI-TB) (for local disease). First, the investigators will compare the results of whole-body MRI to existing imaging tests (bone-scan, and choline PET/CT) that try to find distant spread. Second, the investigators will compare the results of MRI-TB to a very detailed and accurate biopsy of the prostate called template prostate mapping which will show us where and how aggressive the cancer is. Third, if the cancer is confined to the prostate, the investigators will treat men using focal salvage therapies HIFU and cryotherapy. The investigators believe that these new imaging tests could better identify those who will benefit from early hormone treatment and those who will benefit from local salvage treatment. Our study may help justify carrying out a larger trial looking at how good the treatment is in controlling cancer in the medium and long-term.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Progression of Prostate Cancer
Keywords
Biochemical Failure, Radiotherapy, Radiorecurrent Prostate Cancer, MRI Prostate, Whole Body MRI, Bone Scan, Choline PET, Focal Salvage Treatment, HIFU, Cryotherapy

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Model Description
Whole-body MRI and Focal salvage therapy
Masking
Investigator
Allocation
Non-Randomized
Enrollment
177 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Whole body MRI
Arm Type
Experimental
Arm Description
Comparing the detection rate of metastases of whole body MRI compared to current standard of care tests - Choline PET and Bone scan.
Arm Title
MRI Targeted Biopsies
Arm Type
Experimental
Arm Description
Transperineal MRI-targeted biopsies and whole-gland transperineal prostate mapping biopsies
Arm Title
Focal Salvage Therapy
Arm Type
Experimental
Arm Description
Focal salvage HIFU and cryotherapy of recurrent prostate cancer tumors only
Intervention Type
Device
Intervention Name(s)
Whole Body MRI
Other Intervention Name(s)
Philips Ingenia 3.0T Magnetic Resonance System, CE0344
Intervention Description
Full parametric MRI using T1W, T2W, Diffusion-weighted and dynamic-contrast-enhanced images at 3Tesla
Intervention Type
Procedure
Intervention Name(s)
Focal Salvage Therapy
Other Intervention Name(s)
HIFU Device name: Sonablate 500, HIFU Device Serial Number 1049, Cryotherapy Device Name: Seed Net Gold, Cryotherapy Serial Number: Cat No FPRCH 2024
Intervention Description
Cryotherapy and HIFU will be used to targeted the areas of tumor only with a margin of normal tissue.
Intervention Type
Procedure
Intervention Name(s)
MRI Targeted biopsies
Other Intervention Name(s)
SmartTarget software for image-registration
Intervention Description
Image registration will be used to target biopsies followed by full mapping biopsies of the prostate. All biopsies will be carried out transperineally
Primary Outcome Measure Information:
Title
Accuracy of whole body MRI in identifying distant disease
Description
Whole body MRI lesions suspicious of lymph node, visceral or bone metastases compared to standard care tests - Sensitivity, specificity, negative and positive predictive values of whole-body MRI to detect distant disease compared to standard care tests (isotope bone-scan, PET/CT-scan, with skeletal survey where appropriate) and/or pelvic lymphadenectomy and/or biopsy of distant areas in indeterminate cases
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Can multiparametric MRI accurately detect localised recurrent prostate cancer
Description
Imaging of Local Disease Transperineal multi-parametric MRI targeted biopsies compared to Template Prostate Mapping biopsies in the detection of UCL definition 2 clinically significant prostate cancer (Gleason >/=3+4 AND/OR Maximum Cancer Core Length >/=4mm in any one biopsy)
Time Frame
2 years
Other Pre-specified Outcome Measures:
Title
To determine urinary incontinence rates after focal salvage therapy to localised recurrent prostate cancer?
Description
Treatment Continence Presence of urinary incontinence (any pad usage) as determined by the UCLA-EPIC urinary continence questionnaire, at 12 months, in those men with no urinary incontinence at baseline
Time Frame
2 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Previous external beam radiotherapy with or without neo-adjuvant/adjuvant hormone therapy Biochemical failure as defined by the Phoenix criteria (PSA nadir + 2ng/ml) Men considering local salvage treatment for radio-recurrent disease Life expectancy of 5 years or more Exclusion Criteria: Have taken any form of hormones (except 5-alpha reductase inhibitors) within the previous 6 months Unable to have MRI scan as defined by standard care practice Metallic implant likely to cause artefact and reduce scan quality PSA doubling time of 3 months or less PSA value 20ng/ml or greater Prior prostate biopsies following biochemical failure Any prior local intervention to the prostate (e.g., laser/electrical resection or incision, cryotherapy, HIFU, any other ablative modality, any other radiotherapy, any other prostate injection therapy for symptoms or cancer control) Unable to have general or regional anaesthesia Unable to give informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Abi A Kanthabalan, MBChB
Phone
+44(0)2034479194
Email
ana-k@doctors.org.uk
First Name & Middle Initial & Last Name or Official Title & Degree
Hashim U Ahmed, FRCS, PhD
Phone
+44(0)2034479194
Email
hashim.ahmed@ucl.ac.uk
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Hashim U Ahmed, FRCS, PhD
Organizational Affiliation
University College London Hospitals
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Manit Arya, FRCS
Organizational Affiliation
University College London Hospitals
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Mark Emberton, FRCS, MD
Organizational Affiliation
University College London Hospitals
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Shonit Punwani, FRCR
Organizational Affiliation
University College London Hospitals
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hampshire Hospitals NHS Trust
City
London
ZIP/Postal Code
NW1 2BU
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Richard Hindley, FRCS, MD
Email
Richard.Hindley@hhft.nhs.uk
First Name & Middle Initial & Last Name & Degree
Richard Hindley, FRCS, MD
Facility Name
University College London Hospitals
City
London
ZIP/Postal Code
NW1 2BU
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Abi Kanthabalan
Phone
+44(0)34479194
Email
abi-k@doctors.org.uk
First Name & Middle Initial & Last Name & Degree
Hashim U Ahmed, FRCS, PhD

12. IPD Sharing Statement

Citations:
PubMed Identifier
35370021
Citation
Shah TT, Kanthabalan A, Otieno M, Pavlou M, Omar R, Adeleke S, Giganti F, Brew-Graves C, Williams NR, Grierson J, Miah H, Emara A, Haroon A, Latifoltojar A, Sidhu H, Clemente J, Freeman A, Orczyk C, Nikapota A, Dudderidge T, Hindley RG, Virdi J, Arya M, Payne H, Mitra A, Bomanji J, Winkler M, Horan G, Moore CM, Emberton M, Punwani S, Ahmed HU. Magnetic Resonance Imaging and Targeted Biopsies Compared to Transperineal Mapping Biopsies Before Focal Ablation in Localised and Metastatic Recurrent Prostate Cancer After Radiotherapy. Eur Urol. 2022 Jun;81(6):598-605. doi: 10.1016/j.eururo.2022.02.022. Epub 2022 Mar 31. Erratum In: Eur Urol. 2023 Apr;83(4):e117-e118.
Results Reference
derived

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FOcal RECurrent Assessment and Salvage Treatment

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