Assessment Of Dutasteride (AVODART) In Extending The Time To Progression Of Low-Risk, Localized Prostate Cancer In Men

GlaxoSmithKline (GSK)

Status and phase

Completed

Phase 4

Conditions

Neoplasms, Prostate

Treatments

Drug: Dutasteride

Drug: Matching placebo

Study type

Interventional

Funder types

Industry

Identifiers

NCT00363311

AVO105948

Details and patient eligibility

About

The purpose of this study is to examine the effect of dutasteride on the inhibition of low-risk, localized prostate cancer progression in men who would otherwise receive no active therapy (expectant management).

Enrollment

302 patients

Sex

Male

Ages

50 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

Must be male ≥48 and ≤82 years of age
Have biopsy proven, low-risk, localized prostate cancer and active in expectant management not more than 14 months. [For the purposes of assessing subject eligibility a diagnostic biopsy must have included at least 10 cores, (< 4 cores positive and <50% of any one core positive) and must have been obtained within 8 months of screening]. If a saturation biopsy was performed (20 or more cores obtained) 2-3 cores are to be positive for prostate cancer and with <50% of any one core positive. Initial diagnosis of T1a/T1b obtained during a Transrectal ultrasound (TURP) is not allowed.
Gleason score ≤6 [Gleason pattern 4 or above must not be present on any biopsy (initial or entry)]
Clinical stage T1c-T2a
Serum Prostate Specific Antigen (PSA) ≤11ng/mL. If the screening PSA value from the central laboratory is greater than 11ng/ml, one PSA retest is allowed through the central laboratory
A life expectancy greater than five years.
Able to swallow and retain oral medication
Able and willing to participate in the full 3 years of the study
Able to read and write (health outcomes questionnaires are self-administered), understand instructions related to study procedures and give written informed consent.

Exclusion criteria

Subject has ever been treated for prostate cancer with any of the following:
Radiotherapy (external beam or brachytherapy)
Chemotherapy
Hormonal therapy (e.g., megestrol, medroxyprogesterone, cyproterone, diethylstilbestrol (DES)
Oral glucocorticoids
Gonadotropin-releasing hormone (GnRH) analogues (e.g., leuprolide, goserelin)
Glucocorticoids, except inhaled or topical, are not permitted within 3 months prior to visit one
Current and/or previous use of the following medications:
Finasteride (Proscar, Propecia), or Dutasteride (GI198745, AVODART) exposure within 6 months prior to study entry are excluded.
Any other investigational 5α-reductase inhibitors within the past 12 months.
Anabolic steroids (subject must discontinued for 6 months prior to study entry to be eligible)
Drugs with antiandrogenic properties within the past 6 months (e.g,. spironolactone, flutamide, bicalutamide, *cimetidine, *ketoconazole, metronidazole, progestational agents) NOTE: Use of dietary and herbal supplements (e.g., selenium, Vitamin E, saw palmetto) during the study is discouraged but not prohibited. All dietary and herbal supplement usage will be recorded in the case report form (CRF).

*The use of cimetidine is permitted prior to study entry. The use of topical ketoconazole is permitted prior to and during the study.
Prostate volume >80 cc
Subject has had prior prostatic surgery including Transurethral needle ablation of the prostate (TUNA), TURP, Transurethral incision of the prostate (TUIP), laser treatment, thermotherapy, balloon dilatation, prosthesis, and ultrasound ablation within 3 months of enrolment
Severe Benign Prostatic Hyperplasia (BPH) symptoms as manifested by International Prostate Symptom Score (IPSS) symptom score (calculated using the first 7 questions only) of ≥25 or >20 if already on alpha blocker therapy.
Participation in any investigational or marketed drug trial within the 30 days prior to the first dose of study drug or anytime during the study period.
Any unstable serious co-existing medical condition(s) including but not limited to 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 or peptic ulcer disease which is uncontrolled by medical management.
Abnormal liver function test (greater than 2 times the upper limit of normal for alanine aminotransferase [ALT], aspartate aminotransferase [AST], or alkaline phosphatase [ALP]); or bilirubin >1.5 times the upper limit of normal.
Serum creatinine >1.5 times the upper limit of normal.
History of another malignancy within five years that could affect the diagnosis of prostate cancer.
History or current evidence of drug or alcohol abuse within the last 12 months.
History of any illness (including psychiatric) that, in the opinion of the investigator, might confound the results of the study or pose additional risk to the subject.
Known hypersensitivity to any 5α-reductase inhibitor or to any drug chemically related to dutasteride.