Metabolic Impact of Prospective Controlled Mediterranean Type Diets on Prostate Cancer
- Conditions
- Prostate Cancer
- Interventions
- Other: Lower-Carbohydrate Med-t-DietOther: Low-Fat Med-t-Diet
- Registration Number
- NCT05590624
- Lead Sponsor
- Case Comprehensive Cancer Center
- Brief Summary
The purpose of this study is to examine the impact of Mediterranean-type diets on the metabolism of men with localized prostate cancer.
The optimal diet for men with a suspected diagnosis of Prostate Cancer (PCa) is currently unknown. More specifically, the suggested benefits of low carbohydrate and low fat diets in PCa are not determined.
- Detailed Description
Primary Objective
-Evaluate the impact of Mediterranean diets (Med-t-Diets) on non-malignant prostate tissue metabolism
Secondary Objectives
* Evaluate the impact of Med-t-Diets on host metabolism
* Evaluate the impact of Med-t-Diets on systemic biomarkers after consuming Med-t-Diets
* Evaluate the impact of Med-t-Diets on the microbiome and dietary behavior and compliance after consuming Med-t-Diets
Recruitment & Eligibility
- Status
- RECRUITING
- Sex
- Male
- Target Recruitment
- 30
- Males ≥18 years old
- High suspicion of prostate cancer (PCa) per urologist's clinical evaluation
- BMI >18.5
- No prior PCa diagnosis or hormonal therapy (-ies)
- Ability to read, write, speak, and understand English
- Ability to provide informed consent
- Candidate for and elects active surveillance (AS) if diagnostic biopsy is positive
- Willingness to consume provided dietary interventions
- Adequate organ and marrow function: White blood cell count (WBC) ≥2,500/mcL, Absolute neutrophil count (ANC) ≥1,500/mcL, Platelets ≥100,000/mcL, Hemoglobin ≥9 g/dL (transfusions permitted), Total bilirubin ≤1.5 x the institutional upper limit of normal (ULN) (for subjects with Gilbert's disease ≤3.0 mg/dL), Aspartate aminotransferase (AST)/Alanine aminotransferase (ALT) ≤2.5 x institutional ULN, Creatinine clearance ≥51 ml/min as defined by Cockcroft-Gault equation
- Currently consuming a Mediterranean, lower carbohydrate, ketogenic, vegan, vegetarian, high fiber diet (14g fiber > per 1,000 Calories) and/or any supplements (including herbal), vitamins, minerals, that would interfere with diets being tested in the study as determined by dietitian and/or investigators.
- Previous intolerability to fiber-rich diets
- Colitis, Irritable Bowel Syndrome, or other gastrointestinal condition per clinician discretion
- Unwilling to undergo transperineal PCa biopsies
- Food allergies or other major dietary restrictions
- Receiving active medical treatment for Type I or Type II diabetes mellitus
- Prior antibiotic usage (i.e. within last 30 days) at time of consent
- Recent weight loss (both intentional and unintentional) as defined by 5%+ body weight in the last 30 days
- Undergone any type of weight loss surgery
- Any medical contraindications as determined by investigators
- High risk as defined by PSA≥20 and/or PI-RADS 5 lesion as per clinician evaluation
- History of diabetic ketoacidosis
- Gout
- Patients that are immunosuppressed (transplant history, on immunosuppression, etc.) as per clinician discretion
- Recent (within last 30 days) device implant/joint requiring antibiotics as per clinician determination
- Prior history of prostate biopsy infection
- Uncontrolled hypertension as defined by blood pressure greater than 140/80 (with or without medication)
- Gallbladder removed or plan to remove per clinician evaluation
- Other malignancies actively receiving systemic treatment as per clinician evaluation
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- CROSSOVER
- Arm && Interventions
Group Intervention Description Mediterranean-type Diet(s)-Arm 2 Lower-Carbohydrate Med-t-Diet Diet randomization occurs two weeks prior to the Standard of Care (SOC) diagnostic biopsy. If patient is randomized to Arm 2, they will receive Lower Carbohydrate (LC) Mediterranean Diet first. The results of the diagnostic biopsy determines how the patient will proceed on the trial. If there is a confirmed Prostate Cancer (PCa) diagnosis AND is a candidate for Active Surveillance (AS) per SOC, then patient will undergo a washout period and cross-over to the Low Fat (LF) Mediterranean Diet two weeks prior to the SOC confirmatory biopsy. A long-term follow-up (LTFU) visit will occur 3 months after the second dietary intervention has concluded. If patient does not have PCa or is not placed on AS, then they will only have the first dietary intervention and a LTFU visit 3 months after. Mediterranean-type Diet(s)-Arm 2 Low-Fat Med-t-Diet Diet randomization occurs two weeks prior to the Standard of Care (SOC) diagnostic biopsy. If patient is randomized to Arm 2, they will receive Lower Carbohydrate (LC) Mediterranean Diet first. The results of the diagnostic biopsy determines how the patient will proceed on the trial. If there is a confirmed Prostate Cancer (PCa) diagnosis AND is a candidate for Active Surveillance (AS) per SOC, then patient will undergo a washout period and cross-over to the Low Fat (LF) Mediterranean Diet two weeks prior to the SOC confirmatory biopsy. A long-term follow-up (LTFU) visit will occur 3 months after the second dietary intervention has concluded. If patient does not have PCa or is not placed on AS, then they will only have the first dietary intervention and a LTFU visit 3 months after. Mediterranean-type Diet(s)-Arm 1 Low-Fat Med-t-Diet Diet randomization occurs two weeks prior to the Standard of Care (SOC) diagnostic biopsy. If patient is randomized to Arm 1, they will receive Low Fat (LF) Mediterranean Diet first. The results of the diagnostic biopsy determines how the patient will proceed on the trial. If there is a confirmed Prostate Cancer (PCa) diagnosis AND is a candidate for Active Surveillance (AS) per SOC, then patient will undergo a washout period and cross-over to the Lower Carbohydrate (LC) Mediterranean Diet two weeks prior to the SOC confirmatory biopsy. A long-term follow-up (LTFU) visit will occur 3 months after the second dietary intervention has concluded. If patient does not have PCa or is not placed on AS, then they will only have the first dietary intervention and a LTFU visit 3 months after Mediterranean-type Diet(s)-Arm 1 Lower-Carbohydrate Med-t-Diet Diet randomization occurs two weeks prior to the Standard of Care (SOC) diagnostic biopsy. If patient is randomized to Arm 1, they will receive Low Fat (LF) Mediterranean Diet first. The results of the diagnostic biopsy determines how the patient will proceed on the trial. If there is a confirmed Prostate Cancer (PCa) diagnosis AND is a candidate for Active Surveillance (AS) per SOC, then patient will undergo a washout period and cross-over to the Lower Carbohydrate (LC) Mediterranean Diet two weeks prior to the SOC confirmatory biopsy. A long-term follow-up (LTFU) visit will occur 3 months after the second dietary intervention has concluded. If patient does not have PCa or is not placed on AS, then they will only have the first dietary intervention and a LTFU visit 3 months after
- Primary Outcome Measures
Name Time Method Evaluate the impact of Med-t-Diets on non-malignant prostate tissue metabolism Change from diagnostic biopsy (Week 2) at confirmatory biopsy Change in non-malignant prostate tissue metabolomics using mass spectrometry to assess differences in ions/metabolites and corresponding metabolic pathways after different dietary interventions expressed as a fold-change. As an exploratory study, metabolomics will be untargeted and as such is not run with a standard curve and does not have a unit of measure.
- Secondary Outcome Measures
Name Time Method Changes in energy substrate(s) Change from baseline at two weeks on diet Change measured by respiratory exchange ratio (VCO2/VO2) difference between baseline and at two weeks on diet
Changes in blood glucose (mg/dL) Change from baseline at two weeks on diet Change as measured by the difference between blood glucose levels at baseline and at week two on diet
Changes in lipid particle number (nmol/L and/or μmol/L) Change from baseline at two weeks on diet Change measured by the difference in lipid particle number at baseline and at 2 weeks on diet using Nuclear Magnetic Resonance (NMR)
Prostate health changes Change from baseline at two weeks on diet As measured by changes in the Prostate Health Index
Safety and tolerability of the diets Through study completion, an average of 7.5 month Safety and tolerability measured by the number of adverse events and by the gastric tolerance questionnaire
Changes in alpha and beta diversity of the gut microbiome Change from baseline at two weeks on diet Changes measured by Shannon or Simpson diversity index (alpha diversity) and pairwise Bray-Curtis metric values (beta diversity)
Changes in blood metabolomics Change from baseline at two weeks on diet Change in blood metabolomics using mass spectrometry to assess differences in ions/metabolites and corresponding metabolic pathways after different dietary interventions expressed as a fold-change. As an exploratory study, metabolomics will be untargeted and as such is not run with a standard curve and does not have a unit of measure
Changes in ketone levels (mM or mcg/mL) Change from baseline at two weeks on diet Change measured by the difference between ketone levels between baseline and at two weeks on diet
Changes in C-reactive protein (CRP) (mg/L) Change from baseline at two weeks on diet Change measured by the difference between CRP levels at baseline and at 2 weeks on diet
Changes in lipid particle size (nm) Change from baseline at two weeks on diet Change measured by the difference in lipid particle size at baseline and at 2 weeks on diet using Nuclear Magnetic Resonance (NMR).
Diet compliance throughout controlled feeding period(s), two weeks per diet Compliance measured by \>90% of provided calories consumed
Changes in hemoglobin A1C (HbA1C) (%) Change from baseline at two weeks on diet Change measured by the difference between A1C levels at baseline and at 2 weeks on diet
Changes in insulin sensitivity [(Homeostatic Model Assessment of Insulin Resistance (HOMA-IR score)] Change from baseline at two weeks on diet Change as measured by the Homeostatic Model Assessment of Insulin Resistance (HOMA-IR) score using fasting insulin and glucose from longitudinal blood specimens at baseline and at two weeks on diet. The HOMA-IR test tests how resistant a participant is to insulin. A score of less than 1 indicates that a participant is insulin-sensitive, a score greater than 1.9 indicates some insulin resistance, and a score greater than 2.9 indicates significant insulin resistance.
Changes in dietary behavior Through study completion, an average of 7.5 months Behavioral changes measured by validated 24 hour dietary recalls collected by trained dietetics personnel on 2 week days and 1 weekend to capture specific dietary information
Trial Locations
- Locations (1)
Case Comprehensive Cancer Center, Cleveland Clinic Foundation
🇺🇸Cleveland, Ohio, United States