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Brief Title: Perillyl Alcohol in Treating Patients With Metastatic Prostate Cancer That Has Not Responded to Hormone Therapy
Official Title: A Phase II Trial of Perillyl Alcohol (NSC 641066) Administered Daily In Patients With Metastatic Androgen Independent Prostate Cancer
Study ID: NCT00003238
Brief Summary: RATIONALE: Drugs used in chemotherapy use different way to stop tumor cells from dividing so they stop growing or die. PURPOSE: Phase II trial to study the effectiveness of perillyl alcohol in treating patients with metastatic prostate cancer that has not responded to hormone therapy with androgens.
Detailed Description: OBJECTIVES: I. Evaluate the clinical effectiveness of oral perillyl alcohol given to patients with androgen independent metastatic prostate cancer. II. Assess the toxicity of this treatment in these patients. OUTLINE: Patients receive oral perillyl alcohol 4 times a day for 4 weeks. Patients continue treatment in the absence of severe toxicity and disease progression. Patients are followed every 3 months for survival after disease progression. PROJECTED ACCRUAL: This study will accrue 20-40 patients in approximately 2 years.
Minimum Age:
Eligible Ages: CHILD, ADULT, OLDER_ADULT
Sex: MALE
Healthy Volunteers: No
Leonard C. Ferguson Cancer Center, Freeport, Illinois, United States
Green Bay Oncology, Ltd., Green Bay, Wisconsin, United States
Mercy Health System, Janesville, Wisconsin, United States
Gundersen Lutheran Medical Center, La Crosse, Wisconsin, United States
Meriter Hospital, Madison, Wisconsin, United States
University of Wisconsin Comprehensive Cancer Center, Madison, Wisconsin, United States
Sinai Samaritan Medical Center - Milwaukee, Milwaukee, Wisconsin, United States
North Central Oncology Associates, S.C., Wausau, Wisconsin, United States
Name: George Wilding, MD
Affiliation: University of Wisconsin, Madison
Role: STUDY_CHAIR