Efficacy and Safety Study of LE-DT to Treat Metastatic Castrate Resistant Prostate Cancer

Inclusion Criteria

• •1. Be 18 years or older and male.
• •2. Have histologically or cytologically confirmed diagnosis of adenocarcinoma of the prostate.
• •3. Patients without evidence of PSA progression must have clinical or radiographic evidence of metastatic disease.
• •4. Must have castrate levels of testosterone (serum testosterone less than 50ng/dl) by either being on androgen ablation therapy with a luteinizing hormone-releasing hormone (LHRH) agonist or have had a prior bilateral orchiectomy.
• •5. Patients must have documented evidence of disease progression: progressive disease is defined as a minimum of three consecutive elevations in PSA each obtained a minimum of one week apart with the last value being greater than 2 ng/mL and/or new metastatic lesions on bone scan (minimum of 2) and/or new or progressive disease on CT or MRI scan.
• •6. For patients on an antiandrogen (flutamide, nilutamide, bicalutamide)
• •1. If given as part of first line therapy or for patients who did respond to antiandrogen second line therapy, the patient must demonstrate progression of disease at least 4 weeks beyond discontinuation of such agents to rule out an antiandrogen withdrawal response.
• •2. If given as a second line therapy and the patient did not respond or had a decline in PSA for less than 3 months, it is not required to observe for a withdrawal response.
• •7. Chemotherapy-naïve patients (unlimited prior regimens of hormonal therapy are acceptable).
• •8. Have no other malignancy within the past five years, except non-melanoma, skin cancer.
• •9. Have recovered from acute toxicities of prior treatment:
• •1. Greater than or equal to 4 weeks must have elapsed since receiving hormonal therapy (except for chronic non-investigational gonadotropin releasing hormone analogs or other primary androgen suppressive therapy which are required), biologic agents or any investigational agent (palliative bisphosphonate therapy for bone pain can be administered as clinically indicated).
• •2. Greater than or equal to 4 weeks must have elapsed since receiving any radiotherapy
• •3. Greater than or equal to 2 weeks must have elapsed since any prior surgery or granulocyte-stimulating growth factor therapy.
• •10. Have the following hematology levels at Baseline:
• •1. Absolute Neutrophil Count (ANC) greater than or equal to1,500 x 106 cells/L
• •2. Platelets greater than or equal to 100 x 109 cells/L
• •3. Hemoglobin greater than or equal to 9 g/L.
• •11. Have the following chemistry levels at Baseline:
• •1. AST (SGOT), ALT (SGPT) less than or equal to 1.5 x ULN
• •2. Total bilirubin less than or equal to 1.5 ULN
• •3. Creatinine less than or equal to 1.5 ULN; or 24-hour creatinine clearance greater than 60 mL/min
• •4. Normal serum electrolytes and magnesium levels
• •12. Have a life expectancy of greater than or equal to 12 weeks.
• •13. Have an Eastern Cooperative Oncology Group (ECOG) Performance status of 0-2.
• •14. Patient or legal representative must understand the investigational nature of this study and sign an Independent Ethics Committee (EC)/Institutional Review Board (IRB)-approved written informed consent form (ICF) prior to receiving any study related procedure.