NCT Number: NCT00027794
Radical Prostatectomy in Treating Patients With Locally Advanced Prostate Cancer
RATIONALE: Radical prostatectomy may be an effective treatment for locally advanced prostate cancer.
PURPOSE: Phase II trial to study the effectiveness of radical prostatectomy in treating patients who have locally advanced prostate cancer.
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Notify MeKey information
Conditions
Age range
Up to 70 year
Sex eligibility
Male
Study type
Interventional
Phase
Phase 2
Primary location
Virga Jesse Hospital, Hasselt, Belgium
About this study
OBJECTIVES:
- Determine the success rate of radical prostatectomy in patients with locally advanced adenocarcinoma of the prostate.
- Determine the serious toxic event rate of this surgery in these patients.
- Determine the pN status of patients treated with this surgery.
- Determine the percentage of patients found to have organ-confined tumors (pT2) after undergoing this surgery.
- Determine the 2-year prostate-specific antigen-free survival rate of patients treated with this surgery.
- Determine the surgical morbidity rates of patients treated with this surgery.
OUTLINE: This is a multicenter study.
Patients undergo limited pelvic lymphadenectomy and then radical retropubic prostatectomy.
Patients who are found to have pN-positive disease receive further treatment according to the investigator's discretion. Patients with pN0 disease are followed every 3 months for 1 year and then every 4 months for 1 year.
PROJECTED ACCRUAL: A total of 32-74 patients will be accrued for this study.
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
- Unilateral cT3a, cN0, M0
- Well or moderately differentiated tumor
- Gleason score no greater than 7 (4 plus 3 or 3 plus 4)
- Total serum prostate-specific antigen no greater than 20 ng/mL (Hybritech equivalent)
PATIENT CHARACTERISTICS:
Age:
- 70 and under
Performance status:
- WHO 0-1
Life expectancy:
- Not specified
Hematopoietic:
- WBC greater than 3,000/mm^3
- Platelet count greater than 100,000/mm^3
- Hemoglobin greater than 9 g/dL
Hepatic:
- Bilirubin no greater than 1.5 times normal
- ALT or AST less than 3 times normal
- PT and PTT normal
Renal:
- Creatinine no greater than 1.5 mg/dL
Cardiovascular:
- No preexisting uncontrolled cardiac disease, signs of cardiac failure, or rhythm disturbances requiring therapy
- No myocardial infarction within the past 6 months
Pulmonary:
- No gross abnormalities on chest x-ray
Other:
- No other disease that would preclude surgery
- No other prior malignancy except adequately treated basal cell skin cancer
- No other concurrent primary malignancy
- No psychological, familial, sociological, or geographical condition that would preclude compliance
PRIOR CONCURRENT THERAPY:
Biologic therapy:
- Not specified
Chemotherapy:
- Not specified
Endocrine therapy:
- No prior hormonal therapy that would affect assessment of clinical T staging, margin positivity, or definitive pT staging
Radiotherapy:
- No prior pelvic radiotherapy that would affect surgical resectability and perioperative morbidity
Surgery:
- No prior surgery in the small pelvis (vascular surgery, mesh graft hernia repair, any surgery for benign prostatic hypertrophy, or transurethral resection of prostate) that would preclude prostatectomy
Treatment and study plan
Sponsors and collaborators
Lead sponsor
European Organisation for Research and Treatment of Cancer - EORTC
Network
Registry information
Official study title
Radical Prostatectomy for Locally Advanced Prostate Cancer. A Feasibility Study
Important dates
- Study start
- 2001
- Primary completion
- 2005
- First posted
- Jan 27, 2003
- Registry last updated
- Sep 24, 2012
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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