Herbal Therapy for Treatment of Recurrent Prostate Cancer

NCT ID: NCT00669656

Last Updated: 2017-04-20

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 43 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2008-07-06
• Study Completion Date: 2014-10-14

Brief Summary

This study is about Prostate Health Cocktail, a combination supplement that contains vitamin D3, vitamin E, selenium, green tea extract, saw palmetto, lycopene, and soy derivatives. This product is currently available on the market, as herb and vitamin supplements are not regulated by the FDA. Each ingredient has been studied in prostate cancer cells and/or in patients with prostate cancer. At the doses included in this supplement, no serious side effects have been reported.

The purpose of this study is to find out whether Prostate Health Cocktail can lower your PSA. Additionally, we will be looking to see whether taking this treatment causes any unexpected side effects, and whether certain blood tests can inform us about your disease status in addition to your PSA

Detailed Description

Objectives of this study are:

• To assess the PSA response in prostate cancer patients who have a PSA-only disease recurrence after curative local therapy, during treatment with a combination herbal supplement.
• To qualitatively and quantitatively describe the toxicity profile of this herbal supplement.
• To assess changes in PSA doubling time for subjects treated with this supplement.
• To measure tissue GRP78, serum neuroendocrine markers, and circulating tumor cells, for correlation with treatment response and prostate cancer outcomes

Conditions

Prostate Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Prostate Health Cocktail

Group Type: EXPERIMENTAL

Prostate Health Cocktail

Intervention Type: DRUG

3 capsules daily PO up 12 months

Interventions

Prostate Health Cocktail

3 capsules daily PO up 12 months

Intervention Type: DRUG

Other Intervention Names

Cholecalciferol; Vitamin D3; d-alpha tocopherol; vitamin E; L-selenomethionine; selenium; green tea extract; EGC; Epigallocatechin; saw palmetto; lycopene; Isoflavanoids; Daidzein; Genisetein

Eligibility Criteria

Inclusion Criteria

• Age greater than or equal to 18
• Histologically documented adenocarcinoma of the prostate
• Initial treatment with radical prostatectomy or external beam radiation

• Neoadjuvant/Adjuvant Androgen Deprivation therapy allowable, provided it was for a maximum of 24 months, with the last dose of medication at least 12 months previously
• Neoadjuvant or adjuvant chemotherapy allowable, provided it was for a maximum of 6 months, with the last dose of medication at least 12 months previously
• Adjuvant radiation after radical prostatectomy is allowed, provided at least 6 months have elapsed between completion of radiation and enrollment in study
• PSA recurrence, with a rising PSA, as defined by:

• Post Radiation Therapy:

• Absolute PSA >2.0 ng/mL
• PSA nadir <4 ng/mL after radiation
• Absolute rise of at least 0.5 ng/mL total
• At least 2 increases in PSA, separated by at least 2 weeks; these can be separated by a PSA value which declines provided the second rising value is higher than the first rising value.
• Post Prostatectomy:

• Absolute PSA >1.0 ng/mL
• Absolute rise of at least 1 ng/mL total from nadir
• At least 2 increases in PSA separated by at least 2 weeks; these can be separated by a PSA value which declines provided the second rising value is higher than the first value
• PSA Doubling Time (PSA DT) more than 3 months and less than 36 months

• PSA DT to be calculated using the web-based calculator at http://kevin.phys.unm.edu/psa/ with the following constraints:

• At least 3 values, but no more than 6
• All values must be >0.2
• Values must be separated by at least 2 months
• No radiographically evident bony or soft tissue metastases
• Documented discussion between subject and physician about the option to pursue hormone therapy and/or salvage local therapy rather than enroll in this study
• Patients who received treatment with androgen deprivation for biochemical recurrence are eligible provided:

• They did not document castration resistance (defined as 2 rising PSA values while testosteron < 50
• They have been off androgen deprivation for at least 3 months and have recovered their testosterone (>150)
• They have decided,in conjunction with their treating physician that they do not want to resume androgen deprivation
• ECOG Performance Status 0-2
• Life expectancy > 12 months
• Adequate hepatic function (AST, ALT, bilirubin <1.5 x ULN)
• Adequate renal function (eGFR by Cockcroft-Gault or comparable calculation >50 ml/min)
• Willing to discontinue all nutritional supplements and 5-alpha reductase inhibitors (finasteride, dutasteride) for the duration of study treatment, unless the medication is being used to control symptoms of BPH and the patient has been taking the medication for more than 6 weeks
• Willing to discontinue all weight control medications for the duration of study treatment
• Signed informed consent

Exclusion Criteria

• Atypical prostate carcinoma histology (ex: small cell, adenoid cystic)
• Evidence of bony or soft tissue metastatic disease on CT/MRI or bone scan or PET/CT
• Other invasive malignancy within prior 3 years, except for fully treated basal cell or squamous cell carcinoma of the skin.
• Full-dose anticoagulation therapy (warfarin or low molecular weight heparin) or antiplatelet therapy (clopidogrel or ticlopidine), with the exception of low-dose aspirin therapy (81 mg).
• Significant cardiac disease, included but not limited to angina, myocardial infarction, cardiomyopathy, congestive heart failure, and coronary artery disease which has required bypass surgery, angioplasty or stent placement.
• Significant uncontrolled comorbid condition which, in the opinion of the treating physician would compromise the subject's ability to comply with protocol requirements, or would pose undue risk for experiencing adverse events.

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

University of Southern California

OTHER

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Tanya Dorff, MD

Role: PRINCIPAL_INVESTIGATOR

University of Southern California

Locations

USC/Norris Comprehensive Cancer Center

Los Angeles, California, United States

Countries

United States

Other Identifiers

4P-07-3

Identifier Type: -

Identifier Source: org_study_id