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Zoledronate and BMS-275291 in Treating Patients With Prostate Cancer

4 de junio de 2013 actualizado por: National Cancer Institute (NCI)

A Phase II, Open-Label, Randomized Trial of Zoledronic Acid (Zometa™) and BMS-275291 (NSC#713763) in Patients With Hormone Refractory Prostate Cancer

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.

Descripción general del estudio

Descripción detallada

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.

Tipo de estudio

Intervencionista

Inscripción (Actual)

50

Fase

  • Fase 2

Contactos y Ubicaciones

Esta sección proporciona los datos de contacto de quienes realizan el estudio e información sobre dónde se lleva a cabo este estudio.

Ubicaciones de estudio

    • Minnesota
      • Rochester, Minnesota, Estados Unidos, 55905
        • Mayo Clinic

Criterios de participación

Los investigadores buscan personas que se ajusten a una determinada descripción, denominada criterio de elegibilidad. Algunos ejemplos de estos criterios son el estado de salud general de una persona o tratamientos previos.

Criterio de elegibilidad

Edades elegibles para estudiar

18 años y mayores (Adulto, Adulto Mayor)

Acepta Voluntarios Saludables

No

Géneros elegibles para el estudio

Masculino

Descripción

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

Plan de estudios

Esta sección proporciona detalles del plan de estudio, incluido cómo está diseñado el estudio y qué mide el estudio.

¿Cómo está diseñado el estudio?

Detalles de diseño

  • Propósito principal: Tratamiento
  • Asignación: Aleatorizado
  • Modelo Intervencionista: Asignación paralela
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: 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.
Estudios correlativos
Dado IV
Otros nombres:
  • Zometá
  • CGP 42446
  • CGP42446A
  • NDC-zoledronato
  • zoledronato
Given PO
Otros nombres:
  • BMS-275291
  • D2163
Experimental: Arm II (zoledronic acid)
Patients receive zoledronate as in Arm I.
Estudios correlativos
Dado IV
Otros nombres:
  • Zometá
  • CGP 42446
  • CGP42446A
  • NDC-zoledronato
  • zoledronato

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Confirmed response (PSA decline of greater than 50% confirmed at least four weeks apart)
Periodo de tiempo: Up to 2 years
Up to 2 years

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Overall survival time
Periodo de tiempo: From registration to death due to any cause, assessed for up to 2 years
The distribution of survival time will be estimated using the method of Kaplan-Meier.
From registration to death due to any cause, assessed for up to 2 years
Time to disease progression
Periodo de tiempo: From registration to documentation of disease progression, assessed up to 2 years
The distribution of time to progression will be estimated using the method of Kaplan-Meier.
From registration to documentation of disease progression, assessed up to 2 years
Duration of PSA response or duration of PSA control
Periodo de tiempo: Up to 2 years
The distribution of this response duration will be estimated using the method of Kaplan-Meier.
Up to 2 years
Incidence of toxicity as per NCI CTCAE version 2.0
Periodo de tiempo: Up to 2 years
The maximum grade for each type of toxicity will be recorded for each patient, and frequency tables will be reviewed to determine toxicity patterns.
Up to 2 years

Colaboradores e Investigadores

Aquí es donde encontrará personas y organizaciones involucradas en este estudio.

Investigadores

  • Investigador principal: Roberto Pili, Mayo Clinic

Fechas de registro del estudio

Estas fechas rastrean el progreso del registro del estudio y los envíos de resultados resumidos a ClinicalTrials.gov. Los registros del estudio y los resultados informados son revisados ​​por la Biblioteca Nacional de Medicina (NLM) para asegurarse de que cumplan con los estándares de control de calidad específicos antes de publicarlos en el sitio web público.

Fechas importantes del estudio

Inicio del estudio

1 de abril de 2002

Finalización primaria (Actual)

1 de enero de 2005

Fechas de registro del estudio

Enviado por primera vez

6 de junio de 2002

Primero enviado que cumplió con los criterios de control de calidad

26 de enero de 2003

Publicado por primera vez (Estimar)

27 de enero de 2003

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

5 de junio de 2013

Última actualización enviada que cumplió con los criterios de control de calidad

4 de junio de 2013

Última verificación

1 de junio de 2013

Más información

Términos relacionados con este estudio

Otros números de identificación del estudio

  • NCI-2012-02799
  • MC0151
  • N01CM17104 (Subvención/contrato del NIH de EE. UU.)

Esta información se obtuvo directamente del sitio web clinicaltrials.gov sin cambios. Si tiene alguna solicitud para cambiar, eliminar o actualizar los detalles de su estudio, comuníquese con register@clinicaltrials.gov. Tan pronto como se implemente un cambio en clinicaltrials.gov, también se actualizará automáticamente en nuestro sitio web. .

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