Non-Invasive Biomarkers in Prostate Cancer Disease Management

Clinicaltrials.gov ID: NCT06144619
db-list-check Status RECRUITING
b-loader Phase
b-people Age 35 - 85 Years
b-bullseye-arrow Enrollments 500

Conditions

Prostate Cancer

Summary

This study is an observational retrospective/ prospective study with diagnosed low/intermediate risk (no-surgery) & high risk (surgery) prostate cancer that are eligible and willing to undergo standard of care (SOC) assessment, annually along with biopsies, bio-fluid collection. Participants will obtain genomic and histological evaluation on their biopsied samples. Study follows SOC collection with additional body fluid collection (blood, urine). Biopsy/surgery will not require additional sample collection

Locations

1 location Found with status Recruiting

Status

  • RECRUITING

Contact Person

Principal Investigator

  • Yoganand Balagurunathan, PhD

Eligibility Criteria

Inclusion Criteria:

* Prostate cancer patients who had received primary diagnosis at Moffitt or outside the cancer center with available records (radiology, pathology, access to samples).
* No-Surgery (Intermediate risk) group: patients diagnosed with pre-biopsy mpMRI, blood plasma: the biopsy must consist of a pathological diagnosis with a Gleason pattern score.
* Surgery (High risk) group: patients who had radical prostatectomy (RP) with (or with-out) mpMR imaging, bio fluids available for research will be accrued for this group. We follow the NCCN recommendations for high-risk (Unfavorable intermediate risk or High-risk) groups inclusion and follow-up criteria (58, 89, 90).
* ≥ 4 ng/ml and ≤ 20 ng/ml and PSA ≤ 10 ng/ml (for late disease), within 3 months of study enrollment.
* Age 35 through 85 years.
* Zubrod/ECOG performance status <2;
* Ability to understand and willingness to sign a written informed consent document.
* Patients who agree to have a multiparametric MRI with targeted/template biopsy.
* Patients must agree to fill out the longitudinal psychosocial questionnaires assessing health related quality of life.
* Availability of Bio-samples (blood plasma, urine) for exosomal, proteomic, genomic and pathology (H&E slides, IHC slides).
* Quantity of bio-samples; Blood, Urine, tissue sections (including FFPE) for each region of interest.

Exclusion Criteria:

* Subject is not a candidate for multiparametric MRI with contrast. Some reasons may include (but are not limited to): renal insufficiency, foreign body or pacemakers.
* No prior pelvic radiotherapy
* No prior surgery to the prostate, other than transurethral procedures for benign prostatic hyperplasia (e.g., transurethral resection, green light laser treatment)
* No concurrent, active malignancy, other than non-metastatic skin cancer of any type, superficial bladder cancer, or early-stage chronic lymphocytic leukemia (well-differentiated small cell lymphocytic lymphoma) or > Bilateral hip replacement.

Study Plan

Intermediate risk group (no-surgery)

Participants diagnosed with pre-biopsy mpMRI.

  • GENETIC:

    Genomic and Histological Evaluation

    Description:

    Participants will obtain genomic and histological evaluation on their biopsied samples. (Follows SOC)

High-risk group (surgery)

Participants who had radical prostatectomy (RP) with (or with-out) mpMR imaging.

  • GENETIC:

    Genomic and Histological Evaluation

    Description:

    Participants will obtain genomic and histological evaluation on their biopsied samples. (Follows SOC)

Outcome Measures

Primary Outcome Measures

Disease Progression

Time Frame: Up to 3 years

Timeline

  • Last Updated
    September 19, 2024
  • Start Date
    November 22, 2023
  • Today
    January 16, 2025
  • Completion Date ( Estimated )
    January 31, 2029

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