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

Prostate Adenocarcinoma Clinical Trial

Official title:

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

Clinical Trial Details — Status: Active, not recruiting

Administrative data

• NCT number: NCT03654638
• Other study ID #: OSU-12042
• Secondary ID: NCI-2018-00808R0
• Status: Active, not recruiting
• Phase: Phase 2
• Start date: August 15, 2018
• Est. completion date: March 1, 2025

Study information

• Verified date: February 2024
• Source: Ohio State University Comprehensive Cancer Center
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

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.

Description:

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.

Recruitment information / eligibility

• Status: Active, not recruiting
• Enrollment: 25
• Est. completion date: March 1, 2025
• Est. primary completion date: March 9, 2022
• Accepts healthy volunteers: No
• Gender: Male
• Age group: 18 Years and older

Eligibility

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)

Related Conditions & MeSH terms

• Adenocarcinoma
• Prostate Adenocarcinoma

Intervention

Combination Product:
• Dietary Intervention
The dietary intervention requires men to consume 2 slices soy bread each day for 20 weeks while initiating hormone therapy
• Dietary Intervention
The dietary intervention requires men to consume 2 slices wheat bread each day for 20 weeks while initiating hormone therapy

Other:
• Questionnaire Administration
Ancillary studies

Locations

Country	Name	City	State
United States	Ohio State University Comprehensive Cancer Center	Columbus	Ohio

Sponsors (2)

Lead Sponsor	Collaborator
Ohio State University Comprehensive Cancer Center	National Cancer Institute (NCI)

Country where clinical trial is conducted

United States, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in peripheral blood myeloid derived suppressor cells (MDSC)	A two-sample t-test will be used to compare the differences (log-transformed if necessary to improve normality).	Week 0 to week 20
Primary	Treatment effect on peripheral blood MDSC	Mixed-effects regression models will be used to estimate the treatment effect on peripheral blood MDSC after adjusting for covariates such as age, compliance, and weight. A condition by time (pre versus [vs.] post) interaction will be included to test for a treatment effect. A random effect will be included for each subject to account for the dependency between the pre-post measurements. Correlations (Pearson and Spearman) between measures will be evaluated to determine if positive or negative relationships exist between the measures themselves or the week 0 to week 5 differences (e.g. MSDC vs. T-cell proliferation, MDSC vs. cytokines). Model adequacy and assumptions will be evaluated via residual plots. In the event that model assumptions are violated, outcomes will be transformed or non-parametric methods will be used. Tissue MDSC will be compared using linear regression.	Up to week 20
Primary	Treatment effects in plasma cytokines	Mixed-effects regression models will be used to estimate the treatment effect. Correlations (Pearson and Spearman) between measures will be evaluated to determine if positive or negative relationships exist between the measures themselves or the week 0 to week 5 differences (e.g. MSDC vs. T-cell proliferation, MDSC vs. cytokines). Model adequacy and assumptions will be evaluated via residual plots. In the event that model assumptions are violated, outcomes will be transformed or non-parametric methods will be used.	Up to week 20
Primary	Treatment effects in T-cell proliferation	Mixed-effects regression models will be used to estimate the treatment effect. Correlations (Pearson and Spearman) between measures will be evaluated to determine if positive or negative relationships exist between the measures themselves or the week 0 to week 20 differences (e.g. MSDC vs. T-cell proliferation, MDSC vs. cytokines). Model adequacy and assumptions will be evaluated via residual plots. In the event that model assumptions are violated, outcomes will be transformed or non-parametric methods will be used.	Up to week 20
Primary	Treatment effects in prostate specific antigen (PSA)	Mixed-effects regression models will be used to estimate the treatment effect.	Up to week 20
Secondary	PSA response	Mixed-effects models will be used to explore treatment effects in PSA outcomes	Up to week 20

External Links

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