Benefits of Adherence to 5-alpha Reductase Inhibitor Treatment in Men With Enlarged Prostate: An Assessment of Medicare and Medicaid Patients Using the MarketScan Database

Sponsor
GlaxoSmithKline (Industry)
Overall Status
Completed
CT.gov ID
NCT01376258
Collaborator
(none)
28,903
2

Study Details

Study Description

Brief Summary

Adherence and length of treatment with a 5-alpha reductase inhibitor (5ARI) therapy may be associated with improved clinical outcomes for patients with enlarged prostates (EP) and lower health care related costs.

The objectives of this study are to quantify 1.) the relationship between 5ARI adherence and length of therapy and the likelihood of acute urinary retention (AUR), prostate-related surgery (emergency and non-emergency), and clinical progression (defined as AUR and/or prostate-related surgery); and 2.) the monthly EP-related, medical costs in a Medicaid and Medicare population. The null hypothesis is that no differences will be observed in the outcomes and costs of patients who adhere to long-term 5ARI therapy and those who do not. The test hypothesis is that patients with higher levels of adherence to 5ARI for a longer period of time will experience significantly fewer adverse outcomes and significantly lower treatment costs.

The data source for this analysis is the MarketScan database, which contains medical and pharmacy claims for commercial health plan members and Medicare recipients. Medical and pharmacy claims data are sourced directly from health plans and employers. The database represents approximately 18 to 20 million individuals annually and nearly 22 million Medicaid enrollees from multiple states. The database includes the Medicare-covered portion of payment, the employer-paid portion, and any out-of-pocket expenses paid by the beneficiary.

The study design is a retrospective cohort analysis. Each patient's index date was defined as the date of the first fill for a 5ARI prescription.

Condition or Disease Intervention/Treatment Phase

Study Design

Study Type:
Observational
Actual Enrollment :
28903 participants
Observational Model:
Cohort
Time Perspective:
Retrospective
Official Title:
Benefits of Adherence to 5-alpha Reductase Inhibitor Treatment in Men With Enlarged Prostate: An Assessment of Medicare and Medicaid Patients Using the MarketScan Database
Study Start Date :
Oct 1, 2010
Actual Primary Completion Date :
Dec 1, 2010
Actual Study Completion Date :
Dec 1, 2010

Arms and Interventions

Arm Intervention/Treatment
Patients adherent to 5-alpha reductase inhibitor (5ARI)

Patients with benign prostate hyperplasia (BPH) who are adherent (as measured by a medication possession ratio (MPR)) based on 3 MPR threshold values of 70%, 75% and 80%

Drug: 5ARI
dutasteride or finasteride
Other Names:
  • Proscar® (finasteride)
  • Avodart® (dutasteride)
  • Patients who are non-adherent to 5ARI therapy

    Patients with BPH who are not adherent to 5ARI therapy as measured by 3 MPR threshold values of 70%, 75%, and 80%

    Drug: 5ARI
    dutasteride or finasteride
    Other Names:
  • Proscar® (finasteride)
  • Avodart® (dutasteride)
  • Outcome Measures

    Primary Outcome Measures

    1. Mean number of patients with a diagnosis code for acute urinary retention (AUR) and/or a procedure code for prostate surgery [1 year following the first therapy date or until an event that signifies clinical progression is observed (whichever occurs first)]

      AUR and prostate surgery are indicative of clinical progression of enlarged prostate (EP)

    Secondary Outcome Measures

    1. Adjusted benign prostatic hyperplasia (BPH)-related costs [1 year following the first therapy date]

      Differences in cost will be compared across cohorts. BPH-related costs include those associated with ICD-9-CM codes 222.2x or 600.xx

    2. Medication Possession Ratio (MPR) [1 year following the first therapy date]

      A measure of medication adherence (compliance and discontinuation) in patients taking monotherapy versus early combination therapy. Discontinuation is defined as a 30-day gap in therapy

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    65 Years and Older
    Sexes Eligible for Study:
    Male
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Male

    • Age 65 or older

    • A diagnostic claim of BPH (ICD-9-CM code 222.2x or 600.xx)

    • A prescription claim for a 5ARI for at least 60 days during the observation period

    • Continuous eligibility for 6 months prior to and at least 91 days after the index date

    Exclusion Criteria:
    • A prostate cancer diagnosis

    • A procedure cost for any prostate-related surgical procedure prior to the index date

    Contacts and Locations

    Locations

    No locations specified.

    Sponsors and Collaborators

    • GlaxoSmithKline

    Investigators

    • Study Director: GSK Clinical Trials, GlaxoSmithKline

    Study Documents (Full-Text)

    None provided.

    More Information

    Publications

    None provided.
    Responsible Party:
    GlaxoSmithKline
    ClinicalTrials.gov Identifier:
    NCT01376258
    Other Study ID Numbers:
    • 113907
    First Posted:
    Jun 20, 2011
    Last Update Posted:
    May 22, 2017
    Last Verified:
    May 1, 2017

    Study Results

    No Results Posted as of May 22, 2017