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NCT Number: NCT06116851

Prostate Metabolism, Cancer Risk and Gut Microbiota

This is a prospective, single center translational multiple cohort study to investigate the association of gut microbiota and prostate cancer.

Recruiting

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Key information

Age range

18 year and older

Sex eligibility

Male

Study type

Observational

Primary location

Turku University Hospital, Turku, Finland

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About this study

Prostate cancer (PCa) is a significant health care system challenge. PCa is the most common male cancer in Finland and most western countries. Interestingly, although the incidence of indolent (latent) PCa is very similar throughout the globe, there is a remarkable global age-adjusted incidence variation (up to 40-fold difference between highest and lowest incidences).

Epidemiological data suggest that aging in men is associated with neoplastic processes in the prostate but only a subset of men will develop a true malignancy potentially affecting their life-span or quality of life. Genetic factors have a significant effect on PCa risk, but very likely life-style (e.g. diet and physical activity) affect PCa risk as well, but the mechanisms mediating protective or harmful effects of life-style remain unclear.

Gut microbiota, i.e. the collection of microbes colonizing the gastrointestinal tract, has been acknowledged to play significant role in many metabolic pathways and pathogenetic processes in the human body. Although there is some evidence suggesting that gut microbiota affects therapy responses (especially androgen deprivation) in PCa, it´s potential role in prostate carcinogenesis is not well documented. Our previous studies suggest that gut microbiota composition is different in men with and without PCa potentially contributing to the Pca risk, and that changes in steroid hormone synthesis may be one mechanism how gut microbiota affects PCa risk.

PROMIC is a prospective, single center translational multiple cohort study to investigate the association of gut microbiota and PCa. The main aim is to validate our preliminary findings of association between gut microbiota and PCa. We also study metabolic characteristics in the gut, systemic circulation, and prostate tissue in men with different gut microbiota signatures. The study is carried out in Turku University Hospital and University of Turku.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Provision of signed and dated informed consent form.
  • Ability and stated willingness to comply with all study procedures and availability for the duration of the study.

Exclusion criteria

  • inability to comply with study procedures or unwillingness to participate in the study.

Treatment and study plan

MRI scan and laboratory visit

Other

Prostate MRI scan is performed according to the protocol used in earlier studies (PMID 31158230). In addition to the PCa diagnostics, the scan will include abdominal imaging to body composition analysis (visceral and subcutaneous fat and psoas muscle). Baseline blood and urine samples are collected in Turku University Hospital laboratory.

Prostate biopsies

Procedure

The visit follows routine outpatient clinic protocol. The results from MRI and laboratory findings are discussed and the potential benefits and harms from prostate biopsies are evaluated. After a mutual decision, prostate biopsies are performed.

Radical prostatectomy and blood, urine and tissue sampling

Procedure

Baseline blood and urine samples are collected at the time of surgery. Robotic assisted laparoscopic prostatectomy (RALP) is performed according to routine protocol. Routine diagnostic histopathological procedures will be followed, and study tissue samples are obtained in the department of pathology.

TURP and blood, urine and tissue sampling

Procedure

Baseline blood and urine samples are collected the time of surgery. TURP is performed according to normal protocol. Routine diagnostic histopathological procedures will be followed in the department of pathology. Additionally, tissue samples (a total of 10 resection chips) will be collected for study analyses. Due to the study, no additional tissue samples are removed, i.e. study samples are from the tissues removed as clinically indicated.

Radical cystoprostatectomy and blood, urine and tissue sampling

Procedure

Baseline blood and urine samples are collected at the time of surgery. Radical cystoprostatectomy is performed according to routine protocol. Routine diagnostic histopathological procedures will be followed, and study tissue samples are obtained in the department of pathology.

Primary outcomes

  1. Gut microbiota signature

    Time frame: immediately before prostate biopsy

    Gut microbiota signature in men with clinically significant prostate cancer, clinically non-significant prostate cancer, and benign prostate histology

Secondary outcomes

  1. Gut metabolomics

    Time frame: immediately before prostate biopsy

    Metabolic characteristics in the gut in men with different gut microbiota signatures

Other outcomes

  1. Systemic circulation metabolomics

    Time frame: immediately before prostate biopsy

    Metabolic characteristics in the systemic circulation in men with different gut microbiota signatures

  2. Prostate tissue metabolomics

    Time frame: immediately before prostate biopsy

    Metabolic characteristics in the prostate tissue in men with different gut microbiota signatures

Study contacts

Contact information is provided by the study sponsor or research team.

Peter J. Bostrom, MD, PhD

CONTACT

[email protected]

+358-2-3135925

Tarja Lamminen, PhD

CONTACT

[email protected]

Sponsors and collaborators

Lead sponsor

Turku University Hospital

Other Gov

Collaborators

  • University of Turku

Registry information

Acronym: PROMIC

Important dates

Study start
2022
Primary completion
2024
Study completion
2026
First posted
Nov 3, 2023
Registry last updated
Nov 3, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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