Status:
WITHDRAWN
Stereotactic Body Radiotherapy (SBRT) With Concurrent Boost for Low- and Intermediate-Risk Prostate Cancer
Lead Sponsor:
Rocky Mountain Cancer Centers
Collaborating Sponsors:
Dr. Dennis Carter
Conditions:
Prostate Cancer
Eligibility:
MALE
18+ years
Phase:
PHASE2
Brief Summary
The purpose of this study is to determine whether stereotactic body radiation therapy (SBRT) with simultaneous boost (higher radiation dose) to areas within the prostate with more prominent cancerous ...
Detailed Description
Standard external beam radiation therapy (EBRT) for low- to intermediate-risk prostate cancer involves several weeks of daily treatment sessions. Stereotactic body radiation therapy (SBRT) is a newer ...
Eligibility Criteria
Inclusion
- Histologically proven diagnosis of prostate adenocarcinoma within one year
- Gleason Score 2-7
- Clinical T-stage T1b-T2c (AJCC 7th Edition)
- Clinical Nx or N0, and Mx or M0
- PSA \< 20 ng/mL
- Low or intermediate risk according to NCCN guidelines: Low: Clinical Stage (CS) T1b-T2a and Gleason 2-6 and PSA \< 10 ng/ml; Intermediate: CS T2b-T2c and Gleason 2-6 and PSA \< 10 ng/ml, or CS T1b-T2a and Gleason 7 and PSA \< 10 ng/ml, or CS T1b-T2a and Gleason 2-6 and PSA 10-20ng/mL
- ECOG performance status 0 or 1
- Has had a pre-treatment PSA drawn within a month of the beginning of protocol therapy
- If androgen-deprivation therapy (ADT) has been initiated, must have a documented pre-ADT PSA; this baseline PSA should not be obtained during following periods: 1) 10-day period following prostate biopsy; 2) within 30 days after discontinuation of finasteride; or 3) within 90 days after discontinuation of dutasteride.
- Has completed a baseline health-related quality of life assessment Extended Prostate Cancer Index Composite questionnaire (EPIC-26)
- Has had a history and physical examination (including digital rectal examination and a formal morbidity assessment via the ACE-27) within 60 days
- Morbidity score (via the ACE-27) of none (0), mild (1) or moderate (2)
- Willing and able to use adequate contraception during protocol treatment and for 3 months after the completion of protocol treatment
Exclusion
- Invasive (carcinoma in situ is allowed) solid or hematologic malignancy (other than this prostate cancer, or basal or squamous skin cancers) in the last 5 years
- Prior prostatectomy or cryotherapy of the prostate
- Prior radiotherapy to the prostate or lower pelvis
- Prior or concurrent cytotoxic chemotherapy for prostate cancer (prior chemotherapy for a different cancer is allowed)
- Implanted hardware near the planning target volume that would prohibit appropriate treatment planning or treatment delivery in the investigator's opinion
Key Trial Info
Start Date :
August 1 2011
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
August 1 2022
Estimated Enrollment :
Patients enrolled
Trial Details
Trial ID
NCT01409473
Start Date
August 1 2011
End Date
August 1 2022
Last Update
February 12 2014
Active Locations (2)
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1
Rocky Mountain Cancer Centers - Aurora
Aurora, Colorado, United States, 80012
2
Rocky Mountain Cancer Centers - Littleton
Littleton, Colorado, United States, 80120