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Two StereoTactic Ablative Adaptive Radiotherapy Treatments for Localized Prostate Cancer (2STAR)

Primary Purpose

Prostate Adenocarcinoma

Status
Active
Phase
Phase 1
Locations
Canada
Study Type
Interventional
Intervention
Stereotactic Ablative Radiation
Sponsored by
Sunnybrook Health Sciences Centre
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Prostate Adenocarcinoma focused on measuring prostate, radiation, stereotactic body radiation

Eligibility Criteria

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

Inclusion Criteria:

  • Informed consent obtained
  • Men >18 years
  • Histologically confirmed prostate adenocarcinoma (centrally reviewed)
  • Low and intermediate risk prostate cancer, defined as clinical stage T1-2b, Gleason Score less than/equal to 7, and PSA less than 20 ng/mL (low risk patients will have refused or felt to be inappropriate for active surveillance)

Exclusion Criteria:

  • Androgen deprivation therapy (LHRH-agonists or antiandrogens)>6 mo
  • Prior pelvic radiotherapy
  • Anticoagulation medication (if unsafe to discontinue for gold seed insertion)
  • Diagnosis of bleeding diathesis
  • Large prostate (>90cm3) on imaging
  • Immunosuppressive medications
  • Inflammatory bowel disease
  • Presence of a hip prosthesis

Sites / Locations

  • Sunnybrook Health Science Centre Odette Cancer Centre

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Stereotactic Ablative Radiation

Arm Description

Stereotactic Ablative Radiation 26 Gy in 2 fractions, once weekly to prostate

Outcomes

Primary Outcome Measures

Quality of Life
To determine the prostate-specific quality of life (QOL) using the Expanded Prostate Cancer Index Composite (EPIC) 37 questionnaire for patients undergoing a 2 fraction SBRT protocol. QOL using the Expanded Prostate Cancer Index Composite (EPIC) will be obtained at baseline, weeks 1, 4, 12, month 6 and every 6 months until year 5.

Secondary Outcome Measures

Full Information

First Posted
January 7, 2014
Last Updated
November 23, 2020
Sponsor
Sunnybrook Health Sciences Centre
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1. Study Identification

Unique Protocol Identification Number
NCT02031328
Brief Title
Two StereoTactic Ablative Adaptive Radiotherapy Treatments for Localized Prostate Cancer
Acronym
2STAR
Official Title
Two StereoTactic Ablative Adaptive Radiotherapy Treatments for Localized Prostate Cancer
Study Type
Interventional

2. Study Status

Record Verification Date
November 2020
Overall Recruitment Status
Active, not recruiting
Study Start Date
January 2014 (Actual)
Primary Completion Date
September 12, 2014 (Actual)
Study Completion Date
September 12, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Sunnybrook Health Sciences Centre

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
You have been asked to consider participating in the study because you have a cancer of the prostate, which is to be treated with external beam radiation. You have chosen or felt not to be a good candidate for just watching your cancer. As your doctor has informed you, this involves delivering small amounts of radiation daily over several weeks. Normally, a small field directed to the prostate gland is given for 7.5 - 8 weeks. In total, 39 days of radiation are delivered. There is now growing evidence that prostate cancer cells may be killed more effectively if higher doses of radiation are delivered everyday (known as hypofractionation). However, the downside to such a strategy is the potential to cause more side effects because normal organs (such as the rectum and bladder) are also exposed to the higher doses. Stereotactic ablative radiotherapy (SABR) is a high-precision technique which has the ability to deliver radiation in a more focused manor, meaning that the radiation dose can be "sculpted" to the prostate gland, while minimizing the amount of radiation to the bladder and rectum. A certain amount of movement of the prostate normally occurs within the body. To make sure that the prostate will not be missed, a margin of tissue around the prostate also needs to be treated. Although a wide margin will ensure that the prostate is included, it will also cause more normal tissue to receive high doses of radiation. This, in turn, would result in more side effects. To reduce the margin needed around the prostate, and side effects, tiny gold seeds measuring 3.0 x 1.2mm will be inserted into the prostate which can be seen using a special type of X-Ray camera called a portal imager during treatment. This will allow for targeting of the prostate gland more precisely so that a significantly smaller margin of normal tissue will need to be treated. By using gold seeds in conjunction with SABR, there is the potential to safely deliver a more intensive dose of radiation to the prostate gland without increasing the amount of side effects. In other studies where shorter and more intense courses of radiation have been given using similar high-precision techniques, the side effects of treatment have indeed been no worse than the usual techniques. Over the last 7 years, Sunnybrook researchers have treated over three hundred prostate cancer patients on various research protocols with SABR. In those protocols, patients received 5 SBRT treatments over 29 days and this is currently being compared to 5 SBRT treatments over 11 days in an ongoing randomized study. In the United States, several groups have investigated the 5 SBRT approach in 11 days or less and early findings suggest a good tolerance. The study is being done to determine the side effects, quality of life and efficacy of 2-fraction adaptive SBRT technique (2STAR) in the treatment of low and intermediate risk prostate cancer. All participants will receive the same dose and fractionation scheme.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Adenocarcinoma
Keywords
prostate, radiation, stereotactic body radiation

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 1, Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
30 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Stereotactic Ablative Radiation
Arm Type
Experimental
Arm Description
Stereotactic Ablative Radiation 26 Gy in 2 fractions, once weekly to prostate
Intervention Type
Radiation
Intervention Name(s)
Stereotactic Ablative Radiation
Primary Outcome Measure Information:
Title
Quality of Life
Description
To determine the prostate-specific quality of life (QOL) using the Expanded Prostate Cancer Index Composite (EPIC) 37 questionnaire for patients undergoing a 2 fraction SBRT protocol. QOL using the Expanded Prostate Cancer Index Composite (EPIC) will be obtained at baseline, weeks 1, 4, 12, month 6 and every 6 months until year 5.
Time Frame
5 years

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Informed consent obtained Men >18 years Histologically confirmed prostate adenocarcinoma (centrally reviewed) Low and intermediate risk prostate cancer, defined as clinical stage T1-2b, Gleason Score less than/equal to 7, and PSA less than 20 ng/mL (low risk patients will have refused or felt to be inappropriate for active surveillance) Exclusion Criteria: Androgen deprivation therapy (LHRH-agonists or antiandrogens)>6 mo Prior pelvic radiotherapy Anticoagulation medication (if unsafe to discontinue for gold seed insertion) Diagnosis of bleeding diathesis Large prostate (>90cm3) on imaging Immunosuppressive medications Inflammatory bowel disease Presence of a hip prosthesis
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Andrew A Loblaw
Organizational Affiliation
Sunnybrook Health Sciences Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sunnybrook Health Science Centre Odette Cancer Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4N 3M5
Country
Canada

12. IPD Sharing Statement

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Two StereoTactic Ablative Adaptive Radiotherapy Treatments for Localized Prostate Cancer

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