ZANTE: Zometa and Taxotere in Hormone Refractory Prostate Cancer

Phase I Study of the Combination of Zoledronic Acid and Docetaxel in Patients With Hormone Refractory Metastatic Prostate Cancer

This phase I trial is studying the side effects and best dose of docetaxel when given with zoledronic acid in patients with bone metastasis from prostate cancer that has not responded to hormone therapy.

Docetaxel has been used alone and in combination with other anti-cancer therapies in the treatment of hormone refractory metastatic prostate cancer. Zoledronic acid has been used in the treatment of bone metastasis from prostate cancer. This is a study of the combination of these two agents. The Zante study will test a dose escalation of docetaxel in association with a predetermined dose of zoledronic acid (2 mg), given every 14 days for a minimum of 6 and maximum of 12 cycles.

Sequence A: Docetaxel on day 1 and zoledronic acid on day 2

Sequence B: Zoledronic acid on day 1 and docetaxel on day 2

Patients are enrolled sequentially in cohorts of 3 for each dose level, and a maximum of 36 patients will be enrolled.

Inclusion Criteria:

• Written informed consent
• Hormone refractory prostate cancer
• Stage IV disease with bone metastasis
• No immunotherapy, hormonal therapy or radiotherapy within the previous month
• Performance status < or = 2 (ECOG)
• Serum creatinine < 1.5 mg/100ml
• Serum bilirubin < or = 1.25 x UNL (upper normal limit) (or < or = 1.5 x UNL in the presence of hepatic metastases); SGOT e SGPT < or = 1.5 x UNL (or < or = 2.5 x UNL in presence of hepatic metastases)
• Left ventricular ejection fraction > or = 50% (measured by cardiac ultrasound or MUGA scan)
• Neutrophils > 1500/mm3; platelets >100000/mm3; hemoglobin >10 g/100 ml· Life expectancy of at least 3 months

Exclusion Criteria:

• Previous malignancies with the exception of radically treated epithelioma
• Previous chemotherapy
• Comorbidities that would, in the Investigator's opinion, contraindicate the use of the drugs in the study
• Uncontrolled Diabetes
• Severe cardiac arrhythmias, severe uncontrolled congestive heart failure, severe ischemic cardiac disease or myocardial infarction within the previous 6 months
• severe infection
• cerebral metastasis
• Pre-existing motor or sensory neurotoxicity > or = grade 2 according to CTC (Common Toxicity Criteria).