Zoledronate and BMS-275291 in Treating Patients With Prostate Cancer

NCT ID: NCT00039104

Last Updated: 2013-06-05

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 50 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2002-04-30

Brief Summary

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.

Detailed Description

PRIMARY OBJECTIVES:

I. To evaluate the confirmed response rate of hormone refractory prostate cancer patients treated with Zometa with BMS-275291.

SECONDARY OBJECTIVES:

I. To evaluate the toxicity profile associated with this treatment in this patient population.

II. To evaluate the overall and progression-free survival associated with this treatment regimen.

III. To explore changes markers for bone turnover, fPYR, fDPYR, and serum samples for cross-linked N-telopeptides from baseline.

IV. To assess changes in bone tumor metabolism after treatment using PET scans. V. To assess changes in MMP-1, MMP-9, VEGF and bFGF from baseline after treatment.

OUTLINE: This is an open-label, multicenter study. Patients are stratified according to prior chemotherapy (yes vs no) and participating center.

ARM I: Patients receive zoledronate IV over at least 15 minutes on day 1 and oral BMS-275291 daily on days 1-28.

ARM II (CLOSED TO ACCRUAL AS OF 10/10/2003): Patients receive zoledronate as in Arm I.

In both arms, courses repeat every 28 days in the absence of disease progression or unacceptable toxicity.

Patients are followed every 3 months until disease progression and then every 6 months for up to 2 years.

Conditions

Adenocarcinoma of the Prostate; Recurrent Prostate Cancer; Stage IV Prostate Cancer

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Arm I (rebimastat, zoledronic acid)

Patients receive zoledronate IV over at least 15 minutes on day 1 and oral BMS-275291 daily on days 1-28.

Group Type: EXPERIMENTAL

rebimastat

Intervention Type: DRUG

Given PO

zoledronic acid

Intervention Type: DRUG

Given IV

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

Arm II (zoledronic acid)

Patients receive zoledronate as in Arm I.

Group Type: EXPERIMENTAL

zoledronic acid

Intervention Type: DRUG

Given IV

laboratory biomarker analysis

Intervention Type: OTHER

Correlative studies

Interventions

rebimastat

Given PO

Intervention Type: DRUG

zoledronic acid

Given IV

Intervention Type: DRUG

laboratory biomarker analysis

Correlative studies

Intervention Type: OTHER

Other Intervention Names

BMS-275291; D2163; CGP 42446; CGP42446A; NDC-zoledronate; zoledronate; Zometa

Eligibility Criteria

Inclusion Criteria

• 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

Exclusion Criteria

• 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

• Minimum Eligible Age: 18 Years
• Eligible Sex: MALE
• Accepts Healthy Volunteers: No

Sponsors

National Cancer Institute (NCI)

NIH

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Roberto Pili

Role: PRINCIPAL_INVESTIGATOR

Mayo Clinic

Locations

Mayo Clinic

Rochester, Minnesota, United States

Countries

United States

Other Identifiers

MC0151

Identifier Type: -

Identifier Source: secondary_id

N01CM17104

Identifier Type: NIH

Identifier Source: secondary_id

View Link

NCI-2012-02799

Identifier Type: -

Identifier Source: org_study_id