Soy Bread Diet in Improving Immune Function in Participants With Prostate Cancer



Status:Recruiting
Conditions:Prostate Cancer
Therapuetic Areas:Oncology
Healthy:No
Age Range:18 - Any
Updated:9/2/2018
Start Date:August 15, 2018
End Date:June 1, 2020
Contact:The Ohio State University Comprehensive Cancer Center
Email:OSUCCCClinicaltrials@osumc.edu
Phone:1-800293-5066

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The Effect of a Soy Bread Diet Intervention on Immune Function in Men With Prostate Cancer

This phase II trial studies the effects of a soy bread versus a wheat bread in improving
immune function in participants who are beginning a course of androgen deprivation therapy
for prostate cancer. Components found in soy foods may influence the immune system in a way
that may be beneficial for prostate cancer prevention and survivorship.

PRIMARY OBJECTIVES:

I. To precisely define the impact of soy on myeloid derived suppressor cells (MDSC) in a
human model clinical trial.

OUTLINE: Participants are randomized to 1 of 2 arms.

ARM I (SOY BREAD): Participants consume 2 slices of soy bread daily for approximately 20
weeks in the absence of unacceptable toxicity. Concurrent with the intervention, participants
will be staring androgen deprivation therapy at the direction of their medical oncologist.

ARM II (WHEAT BREAD): Participants consume 2 slices of wheat bread daily for approximately 20
weeks in the absence of unacceptable toxicity. Concurrent with the intervention, participants
will be staring androgen deprivation therapy at the direction of their medical oncologist.

Inclusion Criteria:

- Have biopsy proven adenocarcinoma of the prostate (no small cell, sarcomatoid, or
other rare subtypes)

- Be planning a course of at least 5 months of androgen deprivation therapy. Patients
who have had androgen deprivation therapy in the past as part of salvage therapy or
primary therapy, but are initiating a new course will be eligible.

- Have a testosterone concentration within normal limits.

- No neoadjuvant hormonal or chemotherapy (other clinical trials) for their prostate
cancer

- Have an Eastern Cooperative Oncology Group (ECOG) performance status of 0-1.

- Have blood, urea, nitrogen (BUN)/creatinine (Cr), liver enzymes, complete blood count
(CBC), and prothrombin time (PT)/partial thromboplastin time (PTT)/international
normalized ratio (INR) within normal limits

- Voluntarily agree to participate and a sign an informed consent document

- Agree to have prostate biopsy blocks provided to the study for evaluation

- Willing to discontinue all current vitamin/mineral supplements

- Not currently be taking complementary or alternative products (i.e. PC-SPES, Saw
Palmetto) that target the prostate or may impact the hormonal environment

- Agree to consume a standardized vitamin and mineral supplement (provided by the study)
and avoid other nutrition, dietary, or alternative medications/supplements for the
duration of the study

Exclusion Criteria:

- Have an active malignancy other than prostate cancer that requires therapy

- No diagnosed hematologic malignancy

- Not currently taking steroid medications (i.e., chronic lymphocytic leukemia [CLL])

- No chronic infection (i.e., human immunodeficiency virus-positive [HIV+])

- No history of organ transplant requiring immunosuppressive medications

- History of nephrolithiasis (renal stones)

- Renal insufficiency with creatinine > 1.8, including anyone on dialysis regardless of
nadir creatinine

- Have certain medical conditions. Have no history of malabsorptive disorders or other
metabolic disorders requiring special diet recommendations (for example, Crohn?s
disease or gluten enteropathy)
We found this trial at
1
site
Columbus, Ohio 43210
Principal Investigator: Steven Clinton, MD
?
mi
from
Columbus, OH
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