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CAPSTONE PROGRAM 1 OAKLAND UNIVERSITY WILLIAM BEAUMONT oakland.edu/medicine 1.

Dec 23, 2015

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Page 1: CAPSTONE PROGRAM 1 OAKLAND UNIVERSITY WILLIAM BEAUMONT oakland.edu/medicine 1.

CAPSTONE PROGRAM1

OAKLAND UNIVERSITY WILLIAM BEAUMONT

oakland.edu/medicine

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Page 2: CAPSTONE PROGRAM 1 OAKLAND UNIVERSITY WILLIAM BEAUMONT oakland.edu/medicine 1.

Clinical Utility of ConfirmMDx for Prostate Cancer in Management

of Suspected Prostate Cancer

1Thanh Huynh, 2Jason Hafron, MD

1Oakland University William Beaumont School of Medicine2William Beaumont Department of Urology

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Page 3: CAPSTONE PROGRAM 1 OAKLAND UNIVERSITY WILLIAM BEAUMONT oakland.edu/medicine 1.

What is the clinical utility of the ConfirmMDx Test for Prostate

Cancer, i.e. do the results of the test change frequency of repeat

biopsies, follow-up visits, and prostate-specific antigen tests?

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Introduction

• Prostate cancer is one of the most common cancers in men

• Prostate-specific antigen tests (PSA), digital rectal exams (DRE), and prostate biopsies are methods of screening and detection

• ConfirmMDx (MDxHealth, Inc, Irvine CA) is an epigenetic assay that helps confirm negative biopsy.

• Will ConfirmMDx results decrease future clinical tests?

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Page 5: CAPSTONE PROGRAM 1 OAKLAND UNIVERSITY WILLIAM BEAUMONT oakland.edu/medicine 1.

Background

• ConfirmMDx for Prostate Cancer is a relatively new test, having come out in May 2012

• Several studies have shown the effectiveness of using epigenetic assays to detect prostate cancer not seen on biopsy1, 2

• One study has shown that ConfirmMDx reduced the rate of repeat prostate biopsies in clinical practice3

• Since ConfirmMDx is a new test, more studies are needed to confirm its clinical utility.

• Want to look at other parameters other than biopsies, such as repeat office visits and PSAs to see if test has clinical utility

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Methods

• Retrospective chart review. • Compare 3 different populations using data collected

from charts of patients at the Michigan Institute of Urology: 1) control group with negative biopsies and no ConfirmMDx test2) negative biopsies with negative ConfirmMDx tests 3) positive biopsies with positive ConfirmMDx tests

• Compare differences between the groups in terms of follow-up visits, biopsies, and PSAs

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MethodsTools/Forms of Analysis

• Use statistical tests to compare treatment in the three groups

• Sample size limited due to the number of patients/charts available to analyze

• Collecting demographic data (age, race, BMI, family history) and clinical data (DRE, PSA, biopsy findings and their dates)

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Challenges/Solutions/Limitations

• Small sample size (~50-100 patients per group) may not be enough data to prove trends in physician behavior

• Using data from one source (Michigan Institute of Urology)

• Limited follow-up times• Ideally, all three groups would be matched

for the main risk factors (e.g. age, race, PSA at biopsy, etc.)

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Results

• Results pending• Hope to find that ConfirmMDx increases

clinical by decreasing the number of follow-up visits, prostate specific antigen tests, and prostate biopsies.

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Concluding Remarks and Discussion

• Most of data has been collected and hoping to perform analysis soon

• ConfirmMDx test could help reduce the number of clinical tests done after biopsy, preventing repeat testing and saving money

• Future work could include larger sample sizes with better matching between groups, and more follow-up time

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• Ayad Khourdaji, MD and Jessica Gibson (MDxHealth)for help with data collection

• MIU Men’s Health Foundation Jeff Murri Scholarship

Acknowledgements

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References1. Stewart G, Van Neste L, Delvenne P, et al. Clinical utility of a multiplexed epigenetic gene assay to detect occult cancer in histopathologically negative prostate biopsies: results of the multicenter MATLOC study. J Urol. 2013; 189: 1110-16.

2. Van Neste L, Herman JG, Otto G, et al. The epigenetic promise for prostate cancer diagnosis. Prostate. 2012; 72: 1248-1261.

3. Wojno KJ, Costa FJ, Cornell RJ, et al. Reduced rate of biopsies observed in ConfirmMDx clinical utility field study. Am Health Drug Benefits. 2014; 7(3): 129-134.

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