Ibrutinib as Neoadjuvant Therapy in Localized Prostate Cancer

Inclusion Criteria

• 18 years of age or older
• ECOG performance status 0 or 1
• Histologically documented adenocarcinoma of the prostate
• Patients must be suitable for and willing to undergo a radical prostatectomy at the completion of study therapy.
• Adequate bone marrow function, defined as:
• WBC >2,500 cells/mm3
• ANC >1,500 cells/mm3
• Hemoglobin >9 mg/dL
• Platelet count >100,000 cells/mm3
• Adequate renal function, defined as serum creatinine 30 mL/min
• Adequate liver function, defined as:
• AST and ALT <2.5x institutional ULN
• Serum bilirubin <1.5x institutional ULN
• Adequate coagulation function, defined as normal PT/INR and PTT
• Ability to understand and willingness to sign a written informed consent document
• Available evaluable archival tumor tissue for correlative studies including assessment of immune infiltration and Btk expression is required. If archival tissue is unavailable, patients must be willing to undergo repeat prostate biopsy. Tissue is considered sufficient for correlative endpoint analyses if they are obtained from at least 2 prostate cores and consist of at least 15 unstained slides from the largest tumor volume and/or highest Gleason score. The availability of archival tissue or consent for repeat prostate biopsy is required for study eligibility; determination of tissue sufficiency is not required for study eligibility.
• The effects of ibrutinib on the developing human fetus is unknown. Men treated or enrolled on this protocol must agree to use adequate contraception prior to the study, for the duration of the study participation, and for 3 months after completion of treatment.

Exclusion Criteria

• Patients with neuroendocrine or small cell features are not eligible.
• Any evidence of metastatic disease. Pre-operative staging will be undertaken per urologic standard of care.
• Any prior use of hormonal therapy, including:
• GNRH agonists or GNRH antagonists (e.g., leuprorelin, degarelix)
• Antiandrogens (e.g., bicalutamide, flutamide, nilutamide)
• Novel androgen-directed therapies (e.g., abiraterone, enzalutamide)
• Any estrogen containing compounds
• 5-alpha reductase inhibitors (e.g., finasteride, dutasteride)
• PC-SPES or PC-x products. Other herbal therapies or supplements will be considered by the Principle Investigator on a case by case basis based on their potential for hormonal or anti-cancer therapies.
• Chemotherapy ≤ 21 days prior to first administration of study treatment and/or monoclonal antibody ≤ 6 weeks prior to first administration of study treatment
• Prior radiation therapy for prostate cancer
• Prior exposure to BTK inhibitors
• Prior investigational therapy for prostate cancer
• Patients may not receive any other concurrent investigational agents while on study.
• Use of systemic steroid therapy within 28 days of study screening. Patients on inhaled or topical steroids are eligible.
• Concurrent systemic immunosuppressive therapy within 21 days of the first dose of study drug.
• Major surgery requiring the use of general anesthetic within 4 weeks of study enrollment
• HIV, active hepatitis B (HBV) or active hepatitis C (HCV)
• Patients with past HBV infection or resolved HBV infection, defined as the presence of hepatitis B core antibody (HBc Ab) and absence of hepatitis B surface antigen (HBsAg) are eligible. HBV DNA must be obtained in these patients prior to day 1 of ibrutinib therapy, but detection of HBV DNA in these patients will not exclude study participation.
• Patients positive for HCV antibody are eligible only if polymerase chain reaction is negative for HCV RNA.
• Inability to swallow capsules or presence of malabsorption syndromes, disease significantly affecting gastrointestinal function, history of resection of the stomach or small bowel, symptomatic inflammatory bowel disease or ulcerative colitis, or partial or complete small obstruction.
• Currently active, clinically significant cardiovascular disease, such as uncontrolled arrhythmia or