NCT Number: NCT00023686
Surgery Versus Internal Radiation in Treating Patients With Stage II Prostate Cancer
RATIONALE: Internal radiation uses radioactive material placed directly into or near a tumor to kill tumor cells. It is not yet known whether surgery is more effective than internal radiation in treating prostate cancer.
PURPOSE: Randomized phase III trial to compare the effectiveness of surgery with that of internal radiation in treating patients who have stage II prostate cancer.
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Notify MeKey information
Conditions
Age range
Up to 75 year
Sex eligibility
Male
Study type
Interventional
Phase
Phase 3
Primary location
Vancouver General Hospital, Vancouver, British Columbia, Canada
About this study
OBJECTIVES:
- Compare overall survival in patients with stage II prostate cancer treated with radical prostatectomy vs brachytherapy.
- Compare metastasis-free survival and probability of survival without symptoms of patients treated with these regimens.
- Compare the side effects of these treatment regimens in these patients.
OUTLINE: This is a randomized study. Patients are randomized to one of two treatment arms.
- Arm I: Patients undergo radical prostatectomy.
- Arm II: Patients undergo brachytherapy with implanted iodine I 125 or palladium Pd 103 seeds Patients are followed every 6 months for 5 years and then annually thereafter.
PROJECTED ACCRUAL: A total of 1,980 patients (990 per treatment arm) will be accrued for this study within 5.5 years.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
DISEASE CHARACTERISTICS:
- Histologically confirmed adenocarcinoma of the prostate within the past 120 days
- T1c-T2a, N0, M0
- No bilateral disease
- Prostate-specific antigen (PSA) no greater than 10 ng/mL
- In patients with prior neoadjuvant hormonal therapy (NHT), PSA must be less than 10 ng/mL prior to therapy
- Gleason score no greater than 6
- Prostate gland less than 60 cc on transrectal ultrasound or with minimal pubic arch interference OR
- Prostate gland 60 cc or greater prior to NHT allowed if prostate size has been reduced to less than 60 cc by NHT
PATIENT CHARACTERISTICS:
Age:
- 75 and under
Performance status:
- ECOG 0-2 OR
- Zubrod 0-2
Renal:
- Creatinine no greater than 3 mg/dL
Cardiovascular:
- No significant cardiovascular disease
- No New York Heart Association class III or IV heart disease
Other:
- No other malignancy within the past 5 years except effectively treated basal cell or squamous cell skin cancer or other malignancy at low risk for recurrence
- No other condition that would preclude study
PRIOR CONCURRENT THERAPY:
Endocrine therapy:
- See Disease Characteristics
- At least 90 days since prior NHT
- Duration of therapy no greater than 120 days
- No concurrent NHT
Radiotherapy:
- No prior radiotherapy to pelvis
Surgery:
- No prior surgery for prostate cancer or benign disease, including:
- Transurethral resection of the prostate
- Transurethral resection of the bladder neck
- Cryotherapy
- Laser ablation
- Microwave therapy
Treatment and study plan
Radiation
RadiationPrimary outcomes
-
overall survival
Time frame: Up to 10 years
Secondary outcomes
-
disease free survival
Time frame: Up to 10 years
Sponsors and collaborators
Lead sponsor
Alliance for Clinical Trials in Oncology
Other
Collaborators
- National Cancer Institute (NCI)
Registry information
Official study title
A Randomized Trial of Radical Prostatectomy Versus Brachytherapy for Patients With T1c or T2a N0 M0 Prostate Cancer
Important dates
- Study start
- 2001
- Primary completion
- 2004
- Study completion
- 2004
- First posted
- Jan 27, 2003
- Registry last updated
- Jul 6, 2016
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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