Behavior-Based Dietary Intervention in Treating Patients With Hormone-Refractory Prostate Cancer
Prostate Cancer

About this trial
This is an interventional treatment trial for Prostate Cancer focused on measuring stage I prostate cancer, stage II prostate cancer, adenocarcinoma of the prostate
Eligibility Criteria
DISEASE CHARACTERISTICS: Histologically confirmed adenocarcinoma of the prostate No small cell component No histologically confirmed and/or demonstrable metastatic or locally recurrent disease by bone scan, chest x-ray, computed tomography (CT) scan, or transrectal ultrasound No clinical symptoms within the past 90 days Documented biochemical failure after radical prostatectomy Prostate-specific antigen must have initially nadired to an undetectable level (< 0.1 ng/mL) after prostatectomy AND is currently rising (0.3-40.0 ng/mL) Serum testosterone > 100 ng/dL PATIENT CHARACTERISTICS: Age Any age Performance status Zubrod 0-1 Life expectancy At least 1 year Hematopoietic Not specified Hepatic Not specified Renal Not specified Other No known allergic reactions to milk or soy products PRIOR CONCURRENT THERAPY: Biologic therapy Not specified Chemotherapy More than 1 year since prior chemotherapy Endocrine therapy More than 1 year since prior hormonal therapy Radiotherapy Not specified Surgery See Disease Characteristics
Sites / Locations
- University of Texas - MD Anderson Cancer Center
Arms of the Study
Arm 1
Arm 2
Experimental
No Intervention
Arm I: Dietary Intervention
Arm II: Observation
Nutritional counseling on a low-fat, high-fiber, soy supplemented diet and behavior-based activities, such as goal-setting, contracting, and stimulus control, once weekly for 6 weeks, every 3 weeks for 33 weeks, and then at weeks 44, 48, and 52.
Observation every 6 weeks for 36 weeks and then every 8 weeks for 18 weeks.