ADAPT-PSA: Anti-inflammatory Drugs and Serum Prostate-Specific Antigen Test

Sponsor
Albany Medical College (Other)
Overall Status
Recruiting
CT.gov ID
NCT05629494
Collaborator
(none)
398
1
2
23.2
17.2

Study Details

Study Description

Brief Summary

Prostate cancer is the most frequently diagnosed cancer in men in the Unites States. Nearly 1 million prostate biopsy procedures are performed in the United States annually and elevated prostate-specific antigen (PSA) level is the primary reason for prostate biopsy in > 90% of cases. However, at the PSA levels which trigger prostate biopsy, often no cancer is found in prostate biopsy specimens. PSA test can be elevated due to reasons other than cancer such as inflammation or natural variation in the level. Investigators plan to treat men with elevated PSA level with over the counter anti-inflammatory medications (ibuprofen, naproxen) to see if the PSA level will decrease to an acceptable level.

Condition or Disease Intervention/Treatment Phase
  • Drug: Ibuprofen or Naproxen
  • Diagnostic Test: PSA test
Phase 4

Detailed Description

It's known that PSA level can be elevated due to reasons other than prostate cancer including benign prostatic hypertrophy, prostatitis or other urinary tract infections, non-infectious inflammation, and physiologic variation over time. Consequently, nearly 50% of prostate biopsy procedures performed due to elevated PSA level do not yield any cancer , but still expose the patients to the risks of the procedure related complications (discomfort/pain, anxiety, bleeding, infection, and cost). Thus, measures to improve the reliability of PSA test, and potentially avoiding unnecessary procedures, are of significant importance to the patient and healthcare system.

It is common practice to check PSA level annually. PSA test results can vary over time, either due to the imprecision in the analysis and/or due to the biologic variability. This can result in an apparent rise in PSA level when no clinically meaningful rise had occurred. Its estimated that the average lab variation in PSA was approximately 6% and the average biologic variation about 14%. This, it is recommended that isolated elevation in PSA level should be confirmed after several weeks, and before proceeding with further interventions, including prostate biopsy.

Sub-clinical, histologic Inflammation (presence of inflammatory cells) within the prostate tissue and its effect on PSA level has been reported in various settings. In two population-based studies, men who were regularly using over the counter (OTC) nonsteroidal anti-inflammatory drugs (NSAIDs, e.g ibuprofen, naproxen) had lower PSA levels compared to non-users.

Currently, two strategies are utilized in clinical practice to ensure that the PSA level is truly elevated:

  1. Repeat PSA test after several weeks or

  2. A short course of OTC NSAIDs, and then repeat PSA test

Investigators propose to conduct a randomized study to determine the effect of NSAIDs on PSA level compared to the biologic variations in PSA level noted upon repeat testing.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
398 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Effect of Non-steroidal Anti-inflammatory Drugs on Serum Prostate Specific Antigen Level
Actual Study Start Date :
Sep 27, 2022
Anticipated Primary Completion Date :
Sep 1, 2023
Anticipated Study Completion Date :
Sep 1, 2024

Arms and Interventions

Arm Intervention/Treatment
Active Comparator: Repeat serum PSA test

Repeat PSA test at 6 (± 1) weeks, without any treatment

Diagnostic Test: PSA test
PSA test will repeated in 6 weeks

Experimental: Treatment with NSAIDS

Treatment with NSAIDS (Ibuprofen 400 mg, 3 times per day or Naproxen 220 mg, twice per day for 10 days), then repeat PSA test at 6 (± 1) weeks

Drug: Ibuprofen or Naproxen
Participants will receive either Ibuprofen 400 mg 3 times per day or Naproxen 220 mg, twice per day for 10 days.
Other Names:
  • Motrin, Naprosyn
  • Diagnostic Test: PSA test
    PSA test will repeated in 6 weeks

    Outcome Measures

    Primary Outcome Measures

    1. Difference in the extent of changes in PSA level between the study groups [6 weeks]

      Difference in PSA, within and between groups

    2. Participants with change in PSA level to below the age-specific PSA threshold [6 weeks]

      To determine if changes in PSA level were sufficient to avoid intervention

    Secondary Outcome Measures

    1. Correlation between the magnitude of change in PSA level and biopsy results [1 year]

      To determine if the PSA changes correlate with the cancer diagnosis

    2. Durability of the change in PSA levels [1 to 1.5 year]

      Serial PSA levels will be examined to determine whether the change in PSA level is transient or durable

    3. Changes in voiding symptoms as measured by the International Prostate Symptom Score [3-12 months]

      Patient reported symptom score, ranging from 0-35 (higher score=worse outcome)

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    18 Years to 80 Years
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • All men with an elevated PSA level (as designated by their medical provider) will be invited to participate in the study
    Exclusion Criteria:
    • Inability to use NSAIDs (allergy, side effects)

    • History of peptic ulcer disease or GI bleeding

    • Any bleeding disorders

    • Chronic kidney disease: eGlomerular Filtration Rate < 45

    • Heart failure, significant heart disease

    • Poorly controlled hypertension

    • Signs or symptoms of urinary tract infections

    • Use of 5-alpha reductase inhibitors (finasteride, dutasteride) within past 6 months

    • History of prostate cancer

    • Urinary tract instrumentation in the past 2 months (catheter, endoscopy)

    • Regular NSAIDs use (> once per week)

    • Daily Aspirin use (325 mg or 81 mg), UNLESS it can be held for the study period

    • Other anti-platelet or anticoagulant therapy

    • Steroids use (except occasionally inhaled formulations)

    • Liver disease, abnormal liver function tests

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Albany Medical Center Albany New York United States 12208

    Sponsors and Collaborators

    • Albany Medical College

    Investigators

    • Principal Investigator: Badar Mian, MD, Albany Medical College

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    Badar M. Mian, Professor of Urology, Albany Medical College
    ClinicalTrials.gov Identifier:
    NCT05629494
    Other Study ID Numbers:
    • RCT-NSAIDS-PSA
    First Posted:
    Nov 29, 2022
    Last Update Posted:
    Dec 2, 2022
    Last Verified:
    Nov 1, 2022
    Individual Participant Data (IPD) Sharing Statement:
    No
    Plan to Share IPD:
    No
    Studies a U.S. FDA-regulated Drug Product:
    Yes
    Studies a U.S. FDA-regulated Device Product:
    No
    Product Manufactured in and Exported from the U.S.:
    No
    Keywords provided by Badar M. Mian, Professor of Urology, Albany Medical College
    Additional relevant MeSH terms:

    Study Results

    No Results Posted as of Dec 2, 2022