Dutasteride in Treating Patients With Prostate Cancer

August 23, 2013 updated by: University College London Hospitals

Single Site, Phase II, Double Blind, Randomized, Placebo Controlled Study of the Effect of Dutasteride (Avodart) 0.5mg on the Volume and Characteristics of Prostate Cancer, as Assessed by Multifunctional Magnetic Resonance Imaging (MRI) With Lower Risk Prostate Cancer Suitable for Active Surveillance. (MAPPED TRIAL)

RATIONALE: Dutasteride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.

PURPOSE: This randomized phase II trial is studying how well giving dutasteride works in treating patients with prostate cancer.

Study Overview

Status

Unknown

Conditions

Intervention / Treatment

Detailed Description

OBJECTIVES:

Primary

  • To evaluate the change in volume of foci of prostate cancer as assessed by T2-weighted MRI, following exposure to dutasteride (Avodart) 0.5 mg daily for six months.

Secondary

  • To determine the change in volume of prostate cancer as determined by gadolinium-enhanced MRI and diffusion-weighted MRI after 6 months of dutasteride 0.5 mg compared to placebo.
  • To determine the change in volume of prostate cancer as determined by T2-weighted MRI, gadolinium-enhanced MRI, and diffusion-weighted MRI after 3 months of dutasteride compared to placebo.
  • To determine the changes in MR characteristics of prostate cancer (perfusion, cell density) between baseline and six months in patients on dutasteride compared to placebo.
  • To determine the change in volume of prostate cancer as assessed by HistoScan transrectal ultrasound between baseline and six months, in patients on dutasteride compared to placebo.
  • To determine the association between the measured prostate cancer volumes on MRI with the measured prostate cancer volumes on HistoScan at baseline and six months in patients on dutasteride compared to placebo.
  • To determine the association between the measured changes in prostate cancer volume using MRI, and the measured changes in prostate cancer volume using HistoScan transrectal ultrasound, at baseline and at six months, in patients on dutasteride compared to placebo.
  • To correlate changes in tumor volume and characteristics seen on MRI with changes seen on HistoScan between baseline and six months in patients on dutasteride compared to placebo.
  • To correlate change in tumor volume and characteristics seen on MRI with histological features as seen on 6-month biopsy (Gleason score and sum, number of cores involved, cancer core length) in patients on dutasteride compared to placebo.

OUTLINE: Patients are randomized to 1 of 2 treatment arms.

  • Arm I: Patients receive oral dutasteride once daily for 6 months. Treatment continues in the absence of unacceptable toxicity.
  • Arm II: Patients receive oral placebo once daily for 6 months. Treatment continues in the absence of unacceptable toxicity.

Patients undergo a multi-sequence MRI at baseline, 3 months, and 6 months and HistoScan transrectal ultrasound at baseline and 6 months. Patients may also undergo a targeted biopsy of the prostate (standard transrectal biopsy plus ultrasound-guided targeting of lesions seen on MRI) at 6 months.

Study Type

Interventional

Enrollment (Anticipated)

42

Phase

  • Phase 2

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Locations

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Eligibility Criteria

Ages Eligible for Study

No older than 78 years (Child, Adult, Older Adult)

Accepts Healthy Volunteers

No

Genders Eligible for Study

Male

Description

DISEASE CHARACTERISTICS:

  • Histologically confirmed prostate cancer, meeting all of the following criteria:

    • Prostate-specific antigen (PSA) < 10.0 ng/mL
    • T1c-T2a disease
    • Gleason sum of 6 or 7 (secondary pattern 4 only)

  • Patients with low risk disease must meet the following criteria:

    • Gleason pattern 3 + 3
    • PSA < 10.0 ng/mL
    • Clinical T2a disease
  • Patients with Gleason secondary pattern 4 (i.e., Gleason Pattern 3 + 4) are eligible but must not have a primary pattern 4, PSA > 10 ng/mL, or clinical T2b disease
  • Measurable disease on MRI of at least 0.2 cc, based on planimetry volume

  • Biopsy-proven disease within 2 years of screening visit

    • No biopsy artifact on MRI scan (minimum 12-week interval between biopsy and baseline MRI)
  • Eligible for active surveillance according to the criteria set out by the National Institute for Health and Clinical Excellence

PATIENT CHARACTERISTICS:

  • ALT and AST ≤ 2 times the upper limit of normal (ULN)
  • Alkaline phosphatase ≤ 2 times ULN
  • Bilirubin ≤ 1.5 times ULN
  • Estimated glomerular filtration rate (eGFR) ≥ 60 mL/min
  • Able to swallow and retain oral medication
  • Able and willing to participate in the study for its duration
  • Able to read and write (health-outcomes questionnaires are written)
  • Able to understand instructions related to study procedures and give written informed consent
  • No history of another malignancy within five years that could affect the diagnosis of prostate cancer
  • No history or current evidence of drug or alcohol abuse within the last 12 months that might confound the results of the study or pose additional risk to the patient
  • No known hypersensitivity to any 5α-reductase inhibitor or to any drug chemically related to dutasteride

  • No contraindication for undergoing gadolinium-enhanced MRI, including any of the following:

    • Inability to see tumor focus of ≥ 0.2 cc on T2 sequences
    • Previous allergic reaction to gadolinium
    • Serum creatinine > ULN
    • Incompatible pacemaker
    • Metal fragments in eyes
    • Hip replacements that give artifact with prostate/pelvis views
    • Any artifact or condition that reduces image quality of MRI (e.g., inability to keep still)

  • No unstable serious co-existing medical condition(s) including, but not limited, to any of the following:

    • Myocardial infarction, coronary bypass surgery, unstable angina, cardiac arrhythmias, clinically evident congestive heart failure, or cerebrovascular accident within 6 months prior to screening visit
    • Uncontrolled diabetes
    • Peptic ulcer disease uncontrolled by medical management

PRIOR CONCURRENT THERAPY:

  • No prior radiotherapy (external-beam or brachytherapy), high-intensity focused ultrasound (HIFU), or photodynamic therapy (PDT)
  • No prior chemotherapy
  • At least 3 months since prior and no concurrent prostatic surgery, including TUNA, TURP, TUIP, laser treatment, thermotherapy, balloon dilatation, prosthesis, and ultrasound ablation

  • No prior oral glucocorticoids

    • Glucocorticoids, except inhaled or topical, are not permitted within 3 months prior to visit one
  • No prior GnRH analogues (e.g., leuprolide, goserelin)
  • No prior or concurrent hormonal treatment (e.g., megestrol, medroxyprogesterone, cyproterone, DES) of prostate cancer

  • No current and/or prior use of the following medications:

    • Finasteride (Proscar, Propecia), or dutasteride (GI198745, AVODART) exposure within 12 months prior to study entry
    • Any other investigational 5α-reductase inhibitors within the past 12 months
    • Anabolic steroids within the past 6 months

    • Drugs with antiandrogenic properties within the past 6 months (e.g., spironolactone, flutamide, bicalutamide, cimetidine, ketoconazole, progestational agents)

      • The use of cimetidine is permitted prior to study entry
      • The use of topical ketoconazole is permitted prior to and during the study
  • No participation in another investigational or marketed drug trial within the 30 days prior to the first dose of study drug or anytime during the study period

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

How is the study designed?

Design Details

  • Primary Purpose: Treatment
  • Allocation: Randomized
  • Masking: Double

What is the study measuring?

Primary Outcome Measures

Outcome Measure
The change in volume of foci of prostate cancer (PC) as assessed by T2-weighted (T2w) MRI between baseline and 6 months

Secondary Outcome Measures

Outcome Measure
The change in volume of PC as determined by gadolinium-enhanced (GE) MRI and diffusion-weighted (DW) MRI at 6 months
The change in volume of PC as determined by T2w MRI, GE MRI, and DW MRI at 3 months
The changes in MR characteristics of PC (perfusion, cell density) between baseline and 6 months
The change in volume of PC as assessed by HistoScan transrectal ultrasound (TRUS) between baseline and 6 months
The association between the measured PC volumes on MRI with the measured PC volumes on TRUS at baseline and 6 months
The association between the measured changes in PC volume using MRI vs TRUS at baseline and 6 months
The association of PC volume change with qualitative changes seen on TRUS between baseline and 6 months
The association between MR changes in volume and characteristics with histological features as seen on 6-month biopsy (Gleason score and sum, number of cores involved, cancer core length)

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

Sponsor

University College London Hospitals

Investigators

  • Principal Investigator: Mark Emberton, MD, FRCS, MBBS, University College London Hospitals

Study record dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Major Dates

Study Start

June 1, 2010

Primary Completion (Anticipated)

January 1, 2012

Study Registration Dates

First Submitted

September 1, 2010

First Submitted That Met QC Criteria

September 1, 2010

First Posted (Estimate)

September 2, 2010

Study Record Updates

Last Update Posted (Estimate)

August 26, 2013

Last Update Submitted That Met QC Criteria

August 23, 2013

Last Verified

August 1, 2011

More Information

Terms related to this study

Keywords

Additional Relevant MeSH Terms

Other Study ID Numbers

  • CDR0000684018
  • UCL-09-0221
  • EUDRACT-2009-012405-18
  • EU-21067

This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.

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