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11C Acetate Imaging Post Prostatectomy

Primary Purpose

Prostate Cancer

Status
Terminated
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
11C Acetate Imaging
Sponsored by
Massachusetts General Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Prostate Cancer focused on measuring Radical Prostatectomy

Eligibility Criteria

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

Inclusion Criteria:

  • Histologically or cytologically confirmed adenocarcinoma of the prostate
  • History of radical prostatectomy
  • Age ≥18 years
  • PSA ≥0.5 and <4.0 ng/mL
  • Abdominal-Pelvic CT scan without evidence of prostate cancer
  • 99mTc MDP bone scan without evidence of prostate cancer
  • Patient and clinician decision to proceed to salvage pelvic radiation therapy

Exclusion Criteria:

  • Presence of known extra-pelvic evidence of prostate cancer
  • Unable to fast for 4 hours
  • Uncontrolled diabetes
  • History of bilateral orchiectomies
  • Ongoing treatment with any systemic therapy intended for the treatment of prostate cancer

Sites / Locations

  • Massachusetts General Hospital

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

11C Acetate Imaging

Arm Description

11C acetate imaging

Outcomes

Primary Outcome Measures

Sensitivity of 11C Acetate PET
Preliminarily demonstrate that the 11C acetate PET imaging of subjects who have experienced PSA relapse after prostatectomy for prostate cancer is more sensitive than currently available imaging techniques. Enrolled participants will have no evidence of recurrent disease on gold-standard imaging with CT abdomen/pelvis and 99mTc MDP bone scan (approximate sensitivity of 0%). The primary outcome is evidence of residual/recurrent disease as demonstrated by 11C acetate PET uptake outside of the prostatectomy bed.

Secondary Outcome Measures

Establish a Preliminary Institutional Experience with 11C Acetate Imaging
To establish a preliminary institutional experience with 11C acetate imaging of men with prostate cancer
Correlate 11C Acetate PET Imaging Findings with PSA Evidence of Response
To descriptively correlate 11C acetate PET imaging findings with PSA evidence of response to subsequent salvage radiation therapy at 3 months and 6 months after the conclusion of radiation

Full Information

First Posted
May 17, 2012
Last Updated
March 17, 2014
Sponsor
Massachusetts General Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT01602783
Brief Title
11C Acetate Imaging Post Prostatectomy
Official Title
Use of 11C Acetate Imaging for Improved Prediction of the Effectiveness of Salvage Pelvic Radiation Post Prostatectomy: A Pilot Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2014
Overall Recruitment Status
Terminated
Why Stopped
Slow accrual; no further funding
Study Start Date
December 2011 (undefined)
Primary Completion Date
February 2014 (Actual)
Study Completion Date
February 2014 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Massachusetts General Hospital

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
This research is being conducted to test an imaging technique that may be able to detect small amounts of prostate cancer that can not be detected by standard imaging. Many patients who are diagnosed with prostate cancer undergo surgery to remove the prostate. After this surgery, some patients have a PSA blood test that reveals a low but detectable level of PSA. This PSA may be produced by cancer cells in one of two locations: (1) near the area where the prostate used to be, or (2) elsewhere in the body. If the cancer is only in the area where the prostate used to be, it can be successfully treated with radiation to that area. If the cancer is elsewhere, radiation is not helpful. Currently, there is no available scan that can detect cancer when the PSA is still so low. The test used in this study is called [11C] acetate PET screening. [11C] acetate is a radioactive tracer that is given by vein to patients before PET scanning. The PET scanner then detects radioactivity from the tracer that is attached to cells within your body and uses this information to create images (pictures) on a computer screen. [11C] acetate PET scanning has been shown in early studies to detect smaller amounts of prostate cancer that can be detected by standard imaging tests such as CT scan and bone scan. If it is successful at detecting very small amounts of prostate cancer, [11C] acetate PET scanning will help doctors identify patients who will benefit from radiation therapy after their prostate has been surgically removed. It will also help them identify patients who have small amounts of prostate cancer in other parts of the body and will not benefit from radiation to the prostate area. This type of PET scan is investigational. "Investigational" means that the scan is still being studied and that research doctors are trying to find out more about it. It also means that the FDA has not approved this type of PET scan for your type of cancer. The information collected by this scan will determine whether this type of scanning is helpful but it will not be used to make decisions about your medical care.
Detailed Description
If you decide to participate in the study and are eligible, you will undergo a single [11C] acetate PET scan. This scan is designed to detect small amounts of your tumor that were not detected by the CT scan or the bone scan. On the day of the scan, you will fast for at least four hours prior to being given the tracer injection by vein. You will then be scanned in the PET scanner. The entire procedure will take approximately 2 hours. The investigators would like to keep track of your medical condition after you have completed your scan. The investigators would like to do this by looking up information in your medical record during the year following the scan to see how you are doing. Checking your condition helps us understand whether the [11C] acetate PET scan will be helpful to other patients in the future.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Prostate Cancer
Keywords
Radical Prostatectomy

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
2 (Actual)

8. Arms, Groups, and Interventions

Arm Title
11C Acetate Imaging
Arm Type
Experimental
Arm Description
11C acetate imaging
Intervention Type
Other
Intervention Name(s)
11C Acetate Imaging
Intervention Description
Single scan
Primary Outcome Measure Information:
Title
Sensitivity of 11C Acetate PET
Description
Preliminarily demonstrate that the 11C acetate PET imaging of subjects who have experienced PSA relapse after prostatectomy for prostate cancer is more sensitive than currently available imaging techniques. Enrolled participants will have no evidence of recurrent disease on gold-standard imaging with CT abdomen/pelvis and 99mTc MDP bone scan (approximate sensitivity of 0%). The primary outcome is evidence of residual/recurrent disease as demonstrated by 11C acetate PET uptake outside of the prostatectomy bed.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Establish a Preliminary Institutional Experience with 11C Acetate Imaging
Description
To establish a preliminary institutional experience with 11C acetate imaging of men with prostate cancer
Time Frame
1 year
Title
Correlate 11C Acetate PET Imaging Findings with PSA Evidence of Response
Description
To descriptively correlate 11C acetate PET imaging findings with PSA evidence of response to subsequent salvage radiation therapy at 3 months and 6 months after the conclusion of radiation
Time Frame
1 year

10. Eligibility

Sex
Male
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically or cytologically confirmed adenocarcinoma of the prostate History of radical prostatectomy Age ≥18 years PSA ≥0.5 and <4.0 ng/mL Abdominal-Pelvic CT scan without evidence of prostate cancer 99mTc MDP bone scan without evidence of prostate cancer Patient and clinician decision to proceed to salvage pelvic radiation therapy Exclusion Criteria: Presence of known extra-pelvic evidence of prostate cancer Unable to fast for 4 hours Uncontrolled diabetes History of bilateral orchiectomies Ongoing treatment with any systemic therapy intended for the treatment of prostate cancer
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Umar Mahmood, MD, PhD
Organizational Affiliation
Massachusetts General Hospital
Official's Role
Principal Investigator
Facility Information:
Facility Name
Massachusetts General Hospital
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Learn more about this trial

11C Acetate Imaging Post Prostatectomy

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