Exogenous Testosterone Plus Dutasteride for the Treatment of Castrate Metastatic Prostate Cancer

Inclusion Criteria:

Patients should have histologically confirmed castration-resistant metastatic prostate cancer with evidence of disease progression. Patients must have been in a castrate state either by orchiectomy or by GnRH analogues for a minimum of one year. In detail, they should meet all of the following criteria:
Adult male > or = to 18 years of age
Histologically confirmed prostate cancer, currently with progressive disease, defined as rising PSA (50% or more increase to a level of 2 ng/mL or more, based on at least 3 PSA determinations obtained at least 1 weeks apart), or 2 new osseous lesions by bone scan, soft tissue disease progression by RECIST 1.1 criteria , or the appearance of new sites of disease (by MRI/CT).

Evidence of metastatic disease, documented within 4 weeks prior to dutasteride treatment initiation, based on a:

CT or MRI of the abdomen and pelvis, and/or
Radionuclide bone scan (in case of findings suspicious for spinal metastasis, MRI of the spine will be performed to rule out epidural disease)
Serum PSA ≥ 2 ng/mL within 4 weeks prior to dutasteride treatment initiation in order to register to the protocol

Normal organ function with acceptable initial laboratory values documented within 4 weeks prior to dutasteride treatment initiation:

WBC > or = to 3000/µL
Platelets > or = to 100,000/µL
Creatinine < or = to 2 mg/dL
Bilirubin < or = to 1.5 X ULN (institutional upper limits of normal)
AST/ALT < or = to 2 X ULN
Karnofsky performance status > or = to 70%
Willingness to undergo serial blood draws for the purpose of measuring CTCs and other biomarkers. MSKCC patients will need to agree to participate in MSKCC protocol 90-040 Molecular studies and clinical correlations in human prostate cancer [PI: Scher]. Also, MSKCC patients will undergo serial imaging by FDHT and FDG PET scans, under protocol 00-095 [18f]-fluoro-2-deoxy-D-glucose and [18f]-dihydro-testosterone PET imaging in patients with progressive prostate cancer (PI: Morris), depending on tracer and scanner time availability. If the study is opened in other centers outside MSKCC, those centers will be exempt from procedures linked to the MSKCC Protocol # 00-095.
ADT treatment for at least 12 months prior to study entry with serum testosterone < 50 ng/dL.
Ability to understand and willingness to sign a written informed consent document

Exclusion Criteria:

Patients meeting any of the following criteria will not be eligible for study entry:
Evidence of small-cell or neuroendocrine pathologic features
Uncontrolled urinary obstruction
Osseous metastatic disease with imminent risk (at the discretion of the treating physician) of pathologic fracture or cord compression (in patients with known spinal metastasis raising concern for cord compression, MRI of the spine should be performed to rule out epidural disease)
Any situation where, at the discretion of the treating physician, a potential "tumor flare" would be life-threatening
Sleep apnea (unless under good control with current treatment)
Polycythemia vera
History of allergic reactions attributed to compounds of similar chemical or biological composition to dutasteride
Uncontrolled intercurrent illness including, but not limited to, ongoing or active infection, symptomatic congestive heart failure, unstable angina pectoris, cardiac arrhythmia, or psychiatric illness or social situation that would compromise compliance with study requirements
Currently active secondary malignancy (as determined by the treating physician) other than non-melanoma skin cancer

Use of the following medications will be prohibited during the study:

Current and/or previous use of the following medications:
Finasteride (Proscar, Propecia) or dutasteride (GI198745, Avodart) exposure within 6 months of study entry.
Anabolic androgenic steroids, including but not limited to testosterone, 17β testosterone esters, methyltestosterone, stanozolol, and danazol (within 6 months of study entry). Corticosteroids, including hydrocortisone, dexamethasone and prednisone are acceptable.
Additional hormonal therapy within 4 weeks of study entry:
Including megestrol, medroxyprogesterone, cyproterone, and DES
Drugs with antiandrogenic properties (eg, spironolactone if > 50mg/d, flutamide, bicalutamide, nilutamide, ketoconazole,* progestational agents) * Includes topical ketoconazole.
Evidence of epidural disease by MRI