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Temsirolimus and Imatinib Mesylate in Treating Patients With Chronic Myelogenous Leukemia

11 de enero de 2013 actualizado por: National Cancer Institute (NCI)

A Phase I Study of CCI-779 in Combination With Imatinib Mesylate in Chronic Myelogenous Leukemia

This phase I trial is studying the side effects and best dose of temsirolimus when given with imatinib mesylate in treating patients with chronic myelogenous leukemia. Drugs used in chemotherapy, such as temsirolimus, work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Imatinib mesylate may stop the growth of cancer cells by blocking some of the enzymes needed for cell growth. Giving temsirolimus with imatinib mesylate may kill more cancer cells

Descripción general del estudio

Descripción detallada

OBJECTIVES:

I. Determine the safety and tolerability of temsirolimus when administered with imatinib mesylate in patients with chronic myelogenous leukemia.

II. Determine potential dose-limiting toxic effects of this regimen in these patients.

III. Determine, preliminarily, hematologic and cytogenetic response rates in patients treated with this regimen.

OUTLINE: This is a multicenter, dose-escalation study of temsirolimus.

Patients receive temsirolimus intravenously (IV) over 30 minutes once on days 1, 8, 15, and 22 and oral imatinib mesylate once daily on days 1-28. Courses repeat every 28 days in the absence of unacceptable toxicity or disease progression. Patients receive 2 additional courses beyond maximal response. Cohorts of 3-6 patients receive escalating doses of temsirolimus until the maximum tolerated dose (MTD) is determined. The MTD is defined as the dose preceding that at which 2 of 3 or 2 of 6 patients experience dose-limiting toxicity.

Patients are followed for survival.

Tipo de estudio

Intervencionista

Inscripción (Actual)

21

Fase

  • Fase 1

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

    • California
      • Orange, California, Estados Unidos, 92868
        • University of California Medical Center At Irvine-Orange Campus

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

Todos

Descripción

Inclusion Criteria:

  • Histologically confirmed chronic myelogenous leukemia (CML)

    • Philadelphia chromosome-positive OR Bcr-Abl-positive disease, meeting 1 of the following criteria:

      • Accelerated phase, defined by at least 1 of the following:

        • 10-19% blasts in the peripheral blood or bone marrow
        • At least 20% basophils in peripheral blood or bone marrow
        • Platelet count < 100,000/mm^3 (unrelated to therapy)
        • Platelet count > 1,000,000/mm^3 (unresponsive to therapy)
        • Increasing splenomegaly AND increasing WBC count (unresponsive to therapy)
        • Clonal evolution
      • Blast phase, defined by 1 of the following:

        • At least 20% blasts in peripheral blood or bone marrow
        • Extramedullary disease
      • Chronic phase, defined by all of the following:

        • Less than 10% blasts in peripheral blood or bone marrow
        • Less than 20% basophils in peripheral blood or bone marrow
        • Platelet count > 100,000/mm^3
        • Absence of clonal evolution
  • May have received and/or failed prior imatinib mesylate therapy

    • Patients not previously treated with imatinib mesylate receive oral imatinib mesylate once daily 14 days before beginning study drug

      • Must be able to tolerate 600 mg per day of imatinib mesylate before starting CCI-779
    • Patients with chronic phase disease must have failed prior imatinib mesylate at a dose ≥ 600 mg/day, as defined by 1 of the following:

      • Must not have achieved or must have lost hematologic response within 3 months after the start of imatinib mesylate
      • Must not have achieved or must have lost cytogenetic response after 6 months of treatment with imatinib mesylate
      • Must not have achieved or must have lost major cytogenetic response after 12 months of treatment with imatinib mesylate
      • Must have lost complete cytogenetic response
  • Bone marrow aspirate and biopsy with cytogenetics and fluorescent in situ hybridization confirming t(9;22) completed within the past 28 days
  • Performance status - SWOG 0-2
  • More than 3 months
  • See Disease Characteristics
  • Bilirubin normal
  • AST and ALT < 2.5 times upper limit of normal (ULN) (5 times ULN if suspected liver involvement with leukemia)
  • Creatinine normal
  • Creatinine clearance > 60 mL/min
  • No symptomatic congestive heart failure
  • No unstable angina pectoris
  • No cardiac arrhythmia
  • Ejection fraction ≥ 50% by echocardiogram or MUGA scan for patients with known positive cardiac history (e.g., heart failure, coronary artery disease, cardiomegaly on prior chest x-ray, or valvular heart disease)
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception
  • Fasting cholesterol ≤ 350 mg/dL
  • Fasting triglycerides ≤ 400 mg/dL
  • No history of allergic reaction attributed to compounds of similar chemical or biologic composition to temsirolimus or imatinib mesylate
  • No active or ongoing infection
  • No psychiatric illness or social situation that would preclude study compliance
  • No other active malignancy except nonmelanoma skin cancer
  • No other uncontrolled illness
  • At least 48 hours since prior interferon alfa for CML
  • At least 6 weeks since prior stem cell transplantation
  • No concurrent biologic agents
  • No concurrent prophylactic colony-stimulating factors
  • At least 24 hours since prior hydroxyurea for CML
  • At least 7 days since prior mercaptopurine or vinca alkaloids for CML
  • At least 7 days since prior low-dose cytarabine (< 30 mg/m^2 every 12-24 hours) for CML
  • At least 14 days since prior homoharringtonine for CML
  • At least 14 days since prior moderate-dose cytarabine (100-200 mg/m^2 for 5-7 days) for CML
  • At least 21 days since prior anthracyclines, mitoxantrone, cyclophosphamide, etoposide, or methotrexate for CML
  • At least 28 days since prior high-dose cytarabine (1-3 g/m^2 every 12-24 hours for 6-12 doses) for CML
  • At least 6 weeks since prior busulfan for CML
  • No concurrent hydroxyurea
  • No other concurrent chemotherapy
  • At least 7 days since prior steroids for CML
  • No prior organ transplantation
  • More than 2 weeks since prior major surgery (e.g., thoracotomy or intra-abdominal surgery)
  • Recovered from all prior therapy
  • Prior experimental therapy allowed provided completion of treatment corresponds to a duration > 5 half-lives of the experimental drug or any known active metabolite before study
  • No concurrent cyclosporine
  • No concurrent anagrelide
  • No concurrent oral anticoagulants, including warfarin
  • No concurrent CYP3A4 inducers or inhibitors
  • No concurrent tacrolimus
  • No concurrent plasmapheresis
  • No concurrent combination antiretroviral therapy for HIV-positive patients
  • No other concurrent investigational agents
  • No other concurrent anticancer therapies

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: N / A
  • Modelo Intervencionista: Asignación de un solo grupo
  • Enmascaramiento: Ninguno (etiqueta abierta)

Armas e Intervenciones

Grupo de participantes/brazo
Intervención / Tratamiento
Experimental: Treatment (imatinib mesylate, temsirolimus)
Patients receive temsirolimus IV over 30 minutes once on days 1, 8, 15, and 22 and oral imatinib mesylate once daily on days 1-28. Courses repeat every 28 days in the absence of unacceptable toxicity or disease progression
Estudios correlativos
Administrado oralmente
Otros nombres:
  • Gleevec
  • CGP 57148
  • Glivec
Dado IV
Otros nombres:
  • Torisel
  • CCI-779
  • inhibidor del ciclo celular 779

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Unacceptable toxicity graded according to the NCI CTCAE version 3.0
Periodo de tiempo: Up to 5 years
Up to 5 years

Medidas de resultado secundarias

Medida de resultado
Medida Descripción
Periodo de tiempo
Enfermedad progresiva
Periodo de tiempo: Hasta 5 años
Hasta 5 años
Supervivencia
Periodo de tiempo: Hasta 5 años
Hasta 5 años
Duration of response
Periodo de tiempo: Up to 5 years
Presented using descriptive statistics.
Up to 5 years

Colaboradores e Investigadores

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

Investigadores

  • Investigador principal: Tiong Ong, University of California Medical Center At Irvine-Orange Campus

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 2005

Finalización primaria (Actual)

1 de junio de 2010

Fechas de registro del estudio

Enviado por primera vez

7 de enero de 2005

Primero enviado que cumplió con los criterios de control de calidad

7 de enero de 2005

Publicado por primera vez (Estimar)

10 de enero de 2005

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

14 de enero de 2013

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

11 de enero de 2013

Última verificación

1 de enero de 2013

Más información

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. .

Ensayos clínicos sobre análisis de biomarcadores de laboratorio

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