Prostasomes as Diagnostic Tool for Prostate Cancer Detection

Sponsor
Hackensack Meridian Health (Other)
Overall Status
Recruiting
CT.gov ID
NCT03694483
Collaborator
Uppsala University, Sweden (Department of Immunology, Genetics and Pathology) (Other)
600
1
72
8.3

Study Details

Study Description

Brief Summary

Prostate cancer is the most frequently diagnosed cancer among men over 50 years old in Western societies, with an incidence that is steadily increasing in most countries. The current, most commonly used biomarker for prostate cancer is prostate specific antigen (PSA), which has well known limitations in accuracy and requires additional testing. However, prostate cancer cells secrete exosomes, also known as prostasomes, which are only detectable in the blood of prostate cancer patients. The presence of prostasomes in the blood is in itself a prostate cancer diagnosis. However, the assay that has been designed for the purification of prostasomes requires additional testing for evaluating its robustness and usefulness in the clinical setting. Additionally, the evaluation of the cargo of the purified prostasomes may provide more information on the nature of the prostate cancer, which may help develop a molecular assay for a prostate cancer liquid biopsy rather than a tissue biopsy. Therefore, the purpose of this study is two-fold: a validation phase where the purification of prostasomes will be tested on plasma collected from prostate cancer patients and a molecular testing phase where the contents of the purified prostasomes will be evaluated on their ability to determine the grade of the prostate tumors.

We will collaborate with Dr. Masood Kamali-Moghaddam at the Uppsala University (Department of Immunology, Genetics and Pathology) for molecular assay processing.

Condition or Disease Intervention/Treatment Phase
  • Diagnostic Test: Genetic analysis for the detection of prostasomes

Study Design

Study Type:
Observational
Anticipated Enrollment :
600 participants
Observational Model:
Cohort
Time Perspective:
Prospective
Official Title:
Quantification and Purification of Circulating Prostasomes as Diagnostic Tool for Prostate Cancer Detection
Actual Study Start Date :
Oct 3, 2018
Anticipated Primary Completion Date :
Oct 1, 2023
Anticipated Study Completion Date :
Oct 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Patient population

Male individuals with elevated PSA and a positive MRI-driven biopsy AND male individuals with diagnosed prostate cancer (but prior to any treatment)

Diagnostic Test: Genetic analysis for the detection of prostasomes
Whole blood will be collected and processed within 2 hours. Samples will be brought to Hackensack University Medical Center and will be centrifuged. The plasma samples will be tested for presence of prostasomes using the ExoPLA (Exosome in situ Proximity Ligation Assay) assay and the prostasomes will be purified for further miRNA sequencing.

Control Population

Male individuals with elevated PSA and a negative MRI-driven biopsy

Diagnostic Test: Genetic analysis for the detection of prostasomes
Whole blood will be collected and processed within 2 hours. Samples will be brought to Hackensack University Medical Center and will be centrifuged. The plasma samples will be tested for presence of prostasomes using the ExoPLA (Exosome in situ Proximity Ligation Assay) assay and the prostasomes will be purified for further miRNA sequencing.

Outcome Measures

Primary Outcome Measures

  1. sensitivity of the prostasome purification methodology [through study completion - up to 24 months]

    true positive rate of the prostasomes purification methodology using the prostasome detection results for each of the patient specimens (cases and controls)

  2. specificity of the prostasome purification methodology [through study completion - up to 24 months]

    true negative rate of the prostasomes purification methodology using the prostasome detection results for each of the patient specimens (cases and controls)

Secondary Outcome Measures

  1. Quantification of the miRNA expression profiles of the purified protostomes both before and after treatment (in patients cohort only) [through study completion - up to 24 months]

    identify the top 20 most frequently expressed miRNA markers and their level of expression in each of the case patient specimens

  2. Time to disease progression(in patient cohort only) [Up to 24 months]

  3. Time to disease relapse (in patient cohort only) [Up to 24 months]

  4. Overall survival (in patient cohort only) [Up to 24 months]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years and Older
Sexes Eligible for Study:
Male
Accepts Healthy Volunteers:
Yes
Inclusion Criteria:
  • Male

  • With elevated PSA or patients with diagnosed prostate cancer

  • 18 years and older

  • Willingness to participate in the study and compliance with protocol requirements

  • Have not received any type of treatment for prostate cancer

Exclusion Criteria:
  • Patients with confirmed or suspected prostate cancer that have already received any type of treatment

  • Patients with another primary cancer within the past five years of prostate cancer diagnosis. However, superficial skin cancers such as basal cell or squamous cell cancers would not exclude a patient.

Contacts and Locations

Locations

Site City State Country Postal Code
1 Hackensack University Medical Center Hackensack New Jersey United States 07601

Sponsors and Collaborators

  • Hackensack Meridian Health
  • Uppsala University, Sweden (Department of Immunology, Genetics and Pathology)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

Responsible Party:
Hackensack Meridian Health
ClinicalTrials.gov Identifier:
NCT03694483
Other Study ID Numbers:
  • Pro2018-0517
First Posted:
Oct 3, 2018
Last Update Posted:
Apr 13, 2022
Last Verified:
Apr 1, 2022
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No
Keywords provided by Hackensack Meridian Health
Additional relevant MeSH terms:

Study Results

No Results Posted as of Apr 13, 2022