Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
Not provided
| Name | Class |
|---|---|
| Bio-Techne Corporation | UNKNOWN |
Not provided
Not provided
Not provided
Not provided
Magnetic resonance imaging (MRI) has become the current standard of care in risk stratifying men with an elevated Prostate-specific antigen (PSA) to determine who needs to undergo prostate biopsy, which is invasive and carries a 3-5% risk of serious infection. Recent data shows the negative predictive value of MRI to be only 77%, indicating that some men may inappropriately forego biopsy based on a negative MRI. Urinary exosomes can be captured and analyzed by the ExosomeDx (ExoDx) Prostate test, a urine based, gene signature derived from PCA3 (prostate cancer antigen 3) and ERG (erythroblast transformation-specific related gene), and SPDEF (SAM pointed domain-containing ETS transcription factor); ExoDx carries a 90% negative predictive value.
The use of ExoDx test among patients with negative MRIs has the potential to improve the risk stratification of patients with an elevated PSA in a way that the Urologist can more accurately determine which patients need to undergo prostate biopsy. In doing so, the Urologist can better risk-stratify which patients should undergo prostate biopsy and be exposed to the associated potential risks, and also be more confident about the safety of foregoing biopsy in those patients with negative MRI and negative ExoDx test.
Not provided
Not provided
Not provided
Not provided
Not provided
| Label | Type | Description | Intervention Names |
|---|---|---|---|
| Participants with elevated or rising PSA | Experimental | Participants who have been diagnosed with an elevated or rising PSA as determined by their urologist, and who have a negative (PIRADS 1 or 2) prostate MRI will be offered enrollment in this trial. ExoDx Study Kit will be collected onsite. Participants will then be scheduled for transrectal ultrasound-guided or transperineal 12-core prostate biopsy as per the standard diagnostic practice. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| Urinary ExoDx test | Device | A urine sample for ExoDx Study Kit will be collected onsite and shipped to Exosome Diagnostic's laboratory. |
|
| Measure | Description | Time Frame |
|---|---|---|
| Sensitivity | Sensitivity is defined as the probability that clinically significant cancer is detected when it is cancer. Sensitivity = true positive cases / true positive cases + false negative cases | duration of study, average 3 months |
| Specificity | Specificity is defined as the probability that clinically significant cancer is not detected when it is not cancer. Specificity = true negative cases / true negative cases + false positive cases | duration of study, average 3 months |
| Measure | Description | Time Frame |
|---|---|---|
| Cancer Detection Rate | Cancer Detection Rate (CDR): Cancer detection rate is defined as the proportion of enrolled patients with histologically Gleason grade group 1+ cancers and as determined by the Investigator. Cancer detection rate = true positive (histologically Gleason grade 1+) / all tests performed | duration of study, average 3 months |
Not provided
Inclusion Criteria:
To be eligible to participate in this study, an individual must meet all the following criteria;
Willingness to participate and provide signed and dated informed consent form
Male (sex)
Age ≥ 18 years
PSA screen-eligible, per investigator discretion
PSA ≥ 2.0 ng/mL and ≤ 10.0 ng/mL
MRI PIRADS score of 1 or 2
ECOG 0-1
Must have a negative urine culture prior to biopsy
No prior prostate biopsies within the last 5 years (biopsy-naïve)
Willingness to undergo a prostate biopsy as part of the diagnostic work-up
Digital rectal exam with no palpable nodules
Exclusion Criteria:
An individual who meets any of the following criteria will be excluded from participation in this study;
All men who present to Mount Sinai Health System urology clinic and, in the course of routine PSA screening, who are found to have an elevated PSA and a negative MRI (PIRADS 1 or 2) will be approached for consideration to participate in this study.
Not provided
Not provided
Not provided
| Name | Role | Phone | Extension | |
|---|---|---|---|---|
| Nikhil Waingankar, MD | Contact | (718) 808-7777 | nikhil.waingankar@mountsinai.org |
| Name | Affiliation | Role |
|---|---|---|
| Nikhil Waingankar, MD | Icahn School of Medicine at Mount Sinai | Principal Investigator |
| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Mount Sinai Beth Israel / Union Square | New York | New York | 10003 | United States |
Individual participant data that underlie the results reported in this article, after deidentification (text, tables, figures, and appendices).
Immediately following publication. No end date.
Researchers who provide a methodologically sound proposal. To achieve aims in the approved proposal. Specify Other Mechanism Email proposal to Principal Investigator.
Not provided
Not provided
| ID | Term |
|---|---|
| D011471 | Prostatic Neoplasms |
| ID | Term |
|---|---|
| D005834 | Genital Neoplasms, Male |
| D014565 | Urogenital Neoplasms |
| D009371 | Neoplasms by Site |
| D009369 | Neoplasms |
Not provided
Not provided
A prospective diagnostic test design will be used to compare the sensitivity of ExoDx with PSA density (H0: SensitivityPSA Density ≤ SensitivityExoDx versus H1: SensitivityPSA Density > SensitivityExoDx) and the specificity (H0: Specificity PSA Density ≤ Specificity ExoDxversus H1: Specificity PSA Density > Specificity ExoDx).
Not provided
Not provided
Not provided
Not provided
| Transrectal ultrasound-guided prostate biopsy | Diagnostic Test | Participants will be scheduled for transrectal ultrasound-guided prostate biopsy as per the standard diagnostic practice after urinary test. |
|
| Transperineal 12-core prostate biopsy | Diagnostic Test | Participants will be scheduled for transperineal 12-core prostate biopsy as per the standard diagnostic practice after urinary test. |
|
| csPCa Detection Rate | csPCa Detection Rate (csCDR): clinically significant cancer detection rate is defined as the proportion of enrolled patients with histologically Gleason grade group 2+ cancers. csPCa detection rate = true positive (histologically Gleason grade 2+) / all tests performed | duration of study, average 3 months |
| Biopsy aversion rate | Biopsy aversion rate is defined as the proportion of patients in whom the biopsy could have been potentially averted using ExosomeDx, as compared to decisions based on PSA density. | duration of study, average 3 months |
| Net Benefit | Decision curve analysis will be used to calculate the net benefit of adding ExoDx to PSA density (including kinetics and density) and MRI in the diagnostic workflow following. Net benefit is calculated across a range of threshold probabilities, defined as the minimum probability of disease at which further intervention would be warranted, as net benefit = sensitivity × prevalence - (1 - specificity) × (1 - prevalence) × w where w is the odds at the threshold probability. | duration of study, average 3 months |
| Diagnostic Accuracy | Accuracy is defined as the potential of ExoDx to correctly detect the presences or absence of disease. Diagnostic Accuracy = (True Positive) + True Negative / All) * 100 | duration of study, average 3 months |
| Positive Predictive Value (PPV) | Positive predictive value is defined as the probability that an elevated ExoDx actually has cancer. Positive Predictive Value = (True Positive)/(True Positive + False Positive) | duration of study, average 3 months |
| Negative Predictive Value (NPV) | Negative predictive value is defined as the probability a negative ExoDx test does not cancer. Negative Predictive Value = (True Negative)/(True Negative + False Negative) | duration of study, average 3 months |
| Mount Sinai West | New York | New York | 10019 | United States |
|
| Mount Sinai Morningside | New York | New York | 10025 | United States |
| Mount Sinai Hospital | New York | New York | 10029 | United States |
|
| Mount Sinai Queens | New York | New York | 11102 | United States |
|
| Mount Sinai Brooklyn | New York | New York | 11234 | United States |
|
| D005832 |
| Genital Diseases, Male |
| D000091662 | Genital Diseases |
| D000091642 | Urogenital Diseases |
| D011469 | Prostatic Diseases |
| D052801 | Male Urogenital Diseases |