Dutasteride in Treating Patients With Prostate Cancer

NCT ID: NCT01193855

Last Updated: 2013-08-26

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 42 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2010-06-30

Brief Summary

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.

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.

Conditions

Prostate Cancer

Keywords

stage IIB prostate cancer; stage IIA prostate cancer

Study Design

• Allocation Method: RANDOMIZED
• Primary Study Purpose: TREATMENT
• Blinding Strategy: DOUBLE

Interventions

dutasteride

Intervention Type: DRUG

gadolinium-chelate

Intervention Type: DRUG

active surveillance

Intervention Type: OTHER

diffusion-weighted magnetic resonance imaging

Intervention Type: PROCEDURE

functional magnetic resonance imaging

Intervention Type: PROCEDURE

prostate biopsy

Intervention Type: PROCEDURE

ultrasound imaging

Intervention Type: PROCEDURE

Eligibility Criteria

Inclusion Criteria

• 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

• Maximum Eligible Age: 80 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

University College London Hospitals

OTHER

Sponsor Role: lead

Principal Investigators

Mark Emberton, MD, FRCS, MBBS

Role: PRINCIPAL_INVESTIGATOR

University College London Hospitals

Locations

University College of London Hospitals

London, England, United Kingdom

Site Status: RECRUITING

Countries

United Kingdom

Facility Contacts

Contact Person

Role: primary

Other Identifiers

UCL-09-0221

Identifier Type: -

Identifier Source: secondary_id

EUDRACT-2009-012405-18

Identifier Type: -

Identifier Source: secondary_id

EU-21067

Identifier Type: -

Identifier Source: secondary_id

CDR0000684018

Identifier Type: -

Identifier Source: org_study_id