Zoledronate and BMS-275291 in Treating Patients With Prostate Cancer

Completed · Phase 2

Conditions studied: Adenocarcinoma of the Prostate, Recurrent Prostate Cancer, Stage IV Prostate Cancer

In brief

Phase II trial to study the effectiveness of combining zoledronate with BMS-275291 in treating patients who have prostate cancer that has not responded to previous hormone therapy. Zoledronate may prevent bone loss and stop the growth of tumor cells in bone. BMS-275291 may stop the growth of tumor cells by blocking the enzymes necessary for cancer cell growth. Combining zoledronate with BMS-275291 may kill more tumor cells.

Key facts

Study ID

NCT00039104

Run by

National Cancer Institute (NCI)

People needed

50

Starts

2002-04-01

Last updated by the study team

2013-06-05

Who can join

Age: 18 and older. Sex: male. Healthy volunteers: not accepted.

You may qualify if…

• Histologically or cytologically confirmed (adeno)carcinoma of the prostate refractory to hormone therapy
• Metastatic bone disease, as documented by bone scan and confirmed by x-rays, CT scan or MRI scan
• Note: Patients may also have measurable disease in the lymph nodes (retroperitoneal, pelvic or inguinal only), prostate and /or prostatic bed; measurable disease is defined as lesions that can be accurately measured in at least one dimension (longest diameter to be recorded) as >= 20 mm =< 21 days prior to registration
• PSA progression defined as two consecutive increases in PSA value over the previous reference value; the first increase of PSA should occur no earlier than one (1) week after the reference measurement; all patients need to demonstrate continued PSA elevation with an increasing PSA four weeks after the required cessation of their antiandrogen treatment; the required cessation period is 4 weeks for flutamide, nilutamide, and Megace-based treatment, and 8 weeks for bicalutamide-based treatment
• One of the following:
• Continuing primary androgen suppression (LHRH agonist)
• Orchiectomy
• WBC >= 2000/mm\^3
• Absolute neutrophil count (ANC) >= 1500/mm\^3
• PLT >= 100,000/mm\^3
• Hgb >= 9.0 g/dL
• Total bilirubin =< institutional upper normal limits (UNL)
• AST =< 1.5 x UNL
• Serum creatinine =< 1.5 x UNL
• PSA >= 5 ng/mL
• Serum testosterone < 50 ng/dL =< 3 months prior to registration
• Estimated life expectancy of >= 6 months
• ECOG Performance Status (PS) 0, 1, or 2
• Capable of understanding the investigational nature, potential risks and benefits of the study and able to provide valid informed consent
• If sexually active, willing to use an accepted and effective method of contraception consistently for the duration of study participation

You may not qualify if…

• Any of the following:
• > 2 prior chemotherapy regimen
• > 2 non-hormonal treatments for metastatic disease (including biologics, gene therapy, angiogenesis inhibitors, etc., but excluding external radiotherapy)
• Prior therapy with a matrix metalloproteinase inhibitor (MMPI)
• Immunotherapy =< 4 weeks prior to study entry
• Biologic therapy =< 4 weeks prior to study entry
• Radiation therapy =< 4 weeks prior to study entry
• Concomitant hormonal treatment (except LHRH)
• Prior use of systemic radiopharmaceuticals such as samarium and strontium
• PC-Spes =< 4 weeks prior to study entry
• Failure to fully recover from adverse effects of prior therapies regardless of interval since last treatment
• Other concurrent chemotherapy, immunotherapy, or radiotherapy directed at the cancer
• Other therapy or supportive care that is considered investigational
• Known CNS metastases
• Known visceral metastases (pulmonary, liver, kidney, splenic lesions); patients with retroperitoneal, pelvic or inguinal lymph node metastases and/or disease in the prostate (or prostatic bed) will not be excluded
• Uncontrolled intercurrent illness including, but not limited to:
• Ongoing or active infection
• Symptomatic congestive heart failure
• Unstable angina pectoris, cardiac arrhythmia
• Psychiatric illness/social situations that would limit compliance with study requirements
• HIV-positive patients receiving combination anti-retroviral therapy
• Prior malignancy except for adequately treated basal cell or squamous cell skin cancer, adequately treated noninvasive carcinomas, or other cancer from which the patient has been disease free for >= 5 years

Where it is running

• Mayo Clinic — Rochester, Minnesota, United States

Full record on ClinicalTrials.gov

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