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Feasibility Trial in Men With Hormone Sensitive Oligometastatic Prostate Cancer (PRORAD)

Primary Purpose

Hormone Sensitive Oligometastatic Prostate Cancer

Status
Withdrawn
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Radical prostatectomy
HDR (19Gy) or SBRT (35-40Gy)
Sponsored by
Dr. Patrick Cheung
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Hormone Sensitive Oligometastatic Prostate Cancer

Eligibility Criteria

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

Inclusion Criteria:

  • Able to provide informed consent.
  • Histologic confirmation of prostate adenocarcinoma.
  • Stage IV disease with ≤ 5 metastases outside of the pelvis.
  • ≤ 3 metastases in any one organ system.
  • ECOG performance 0-1.
  • All metastatic tumours amenable to SBRT.
  • Patient eligible for either RP or RT to the prostate.

Exclusion Criteria:

  • Castration resistant prostate cancer.
  • Previous RP or RT to prostate.
  • Inability to treat all metastases with SBRT.
  • Prior malignancy within the past 5 years, excluding non-melanoma skin cancer, in-situ cancer, superficial bladder cancer, chronic lymphocytic leukemia or low grade lymphoma which is being observed.

Sites / Locations

  • Sunnybrook Health Sciences Centre

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Arm 1

Arm 2

Arm Description

Radical prostatectomy

Radiotherapy

Outcomes

Primary Outcome Measures

Patients willing to accept their randomization
Patients willing to accept their randomization will be measured as a proportion.

Secondary Outcome Measures

Toxicity
Acute and late toxicities will be measured using CTCAE v4.0 and will be reported as percentages.
Efficacy
Time to CRPC will be calculated using Kaplan Meier methodology.
Efficacy
Progression free survival will be calculated using Kaplan Meier methodology.
Efficacy
Local control will be calculated using Kaplan Meier methodology.
Efficacy
Distant control will be calculated using Kaplan Meier methodology.
Efficacy
Overall survival will be calculated using Kaplan Meier methodology.

Full Information

First Posted
January 11, 2017
Last Updated
November 26, 2020
Sponsor
Dr. Patrick Cheung
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1. Study Identification

Unique Protocol Identification Number
NCT03301701
Brief Title
Feasibility Trial in Men With Hormone Sensitive Oligometastatic Prostate Cancer
Acronym
PRORAD
Official Title
Randomized Feasibility Trial of Prostate Radiotherapy vs Prostatectomy in Men With Hormone Sensitive Oligometastatic Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Withdrawn
Why Stopped
Lack of accruals
Study Start Date
September 22, 2017 (Actual)
Primary Completion Date
May 30, 2019 (Actual)
Study Completion Date
May 30, 2019 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Dr. Patrick Cheung

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
Patients with hormone sensitive oligometastatic prostate cancer (≤ 5 metastatic tumours outside of regional pelvic nodes with no more than 3 in any organ system) and no previous treatment to prostate will be treated with intermittent androgen deprivation therapy +/- chemotherapy, stereotactic radiotherapy to all metastases, and either radical prostatectomy or radiotherapy.
Detailed Description
Investigators propose to do a randomized feasibility trial comparing RP vs RT to the prostate in the setting of hormone sensitive oligometastatic prostate cancer. SBRT will be used to treat all of the metastases, and this will be combined with an intermittent ADT approach. Adding systemic chemotherapy will be allowed. Given the past difficulties of randomizing patients between RP and RT in localized prostate cancer studies (like SPIRIT), investigators feel a small feasibility project is the first step. In the setting of metastatic disease, where radical treatment is not routine standard of care, we hope that patients will be more inclined to accept randomization. If patients do not accept their assigned randomization (ie they prefer RP even though they are randomized to RT, or vice versa), they will still be treated with their prostate intervention of choice and followed for their outcomes.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Hormone Sensitive Oligometastatic Prostate Cancer

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Arm 1
Arm Type
Experimental
Arm Description
Radical prostatectomy
Arm Title
Arm 2
Arm Type
Active Comparator
Arm Description
Radiotherapy
Intervention Type
Procedure
Intervention Name(s)
Radical prostatectomy
Intervention Description
Radical prostatectomy
Intervention Type
Radiation
Intervention Name(s)
HDR (19Gy) or SBRT (35-40Gy)
Intervention Description
Patients will receive HDR unless judged to medically unfit to undergo HDR brachytherapy, in which case they will receive SBRT
Primary Outcome Measure Information:
Title
Patients willing to accept their randomization
Description
Patients willing to accept their randomization will be measured as a proportion.
Time Frame
2 years
Secondary Outcome Measure Information:
Title
Toxicity
Description
Acute and late toxicities will be measured using CTCAE v4.0 and will be reported as percentages.
Time Frame
7 years
Title
Efficacy
Description
Time to CRPC will be calculated using Kaplan Meier methodology.
Time Frame
7 years
Title
Efficacy
Description
Progression free survival will be calculated using Kaplan Meier methodology.
Time Frame
7 years
Title
Efficacy
Description
Local control will be calculated using Kaplan Meier methodology.
Time Frame
7 years
Title
Efficacy
Description
Distant control will be calculated using Kaplan Meier methodology.
Time Frame
7 years
Title
Efficacy
Description
Overall survival will be calculated using Kaplan Meier methodology.
Time Frame
7 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Able to provide informed consent. Histologic confirmation of prostate adenocarcinoma. Stage IV disease with ≤ 5 metastases outside of the pelvis. ≤ 3 metastases in any one organ system. ECOG performance 0-1. All metastatic tumours amenable to SBRT. Patient eligible for either RP or RT to the prostate. Exclusion Criteria: Castration resistant prostate cancer. Previous RP or RT to prostate. Inability to treat all metastases with SBRT. Prior malignancy within the past 5 years, excluding non-melanoma skin cancer, in-situ cancer, superficial bladder cancer, chronic lymphocytic leukemia or low grade lymphoma which is being observed.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Patrick Cheung
Organizational Affiliation
Sunnybrook Health Sciences Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sunnybrook Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N3M5
Country
Canada

12. IPD Sharing Statement

Plan to Share IPD
No

Learn more about this trial

Feasibility Trial in Men With Hormone Sensitive Oligometastatic Prostate Cancer

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