Esta página se tradujo automáticamente y no se garantiza la precisión de la traducción. por favor refiérase a versión inglesa para un texto fuente.

Docetaxel, Capecitabine, and Bevacizumab in Treating Patients With Metastatic Breast Cancer

5 de diciembre de 2016 actualizado por: Alliance for Clinical Trials in Oncology

Phase II Trial Of Docetaxel With Capecitabine And Bevacizumab As First-Line Chemotherapy For Patients With Metastatic Breast Cancer

RATIONALE: Drugs used in chemotherapy, such as docetaxel and capecitabine, work in different ways to stop tumor cells from dividing so they stop growing or die. Monoclonal antibodies such as bevacizumab can locate tumor cells and either kill them or deliver tumor-killing substances to them without harming normal cells. Bevacizumab may also stop the growth of tumor cells by stopping blood flow to the tumor. Combining chemotherapy with monoclonal antibody therapy may kill more tumor cells.

PURPOSE: This phase II trial is studying how well giving docetaxel and capecitabine together with bevacizumab works in treating patients with metastatic breast cancer.

Descripción general del estudio

Estado

Terminado

Condiciones

Descripción detallada

OBJECTIVES:

Primary

  • Determine the response rate in patients with metastatic breast cancer treated with docetaxel, capecitabine, and bevacizumab as first-line chemotherapy.

Secondary

  • Determine time to disease progression in patients treated with this regimen.
  • Determine survival of patients treated with this regimen.
  • Determine the toxicity profile of this regimen in these patients.
  • Determine the duration of response in patients treated with this regimen.

OUTLINE: This is a multicenter study.

Patients receive docetaxel IV over 1 hour and bevacizumab IV over 30-90 minutes on day 1. Patients also receive oral capecitabine twice daily on days 1-14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients achieving a complete response (CR) receive at least 2 additional courses beyond CR.

Patients are followed every 3 months for 1 year, every 6 months for 1 year, and then annually for 3 years.

Tipo de estudio

Intervencionista

Inscripción (Actual)

46

Fase

  • Fase 2

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

DISEASE CHARACTERISTICS:

  • Histologically or cytologically confirmed invasive breast cancer

    • Clinical evidence of metastatic disease

      • No bone metastases as the only evidence of metastasis
  • Measurable disease

    • At least 1 lesion ≥ 2.0 cm by CT scan or MRI OR ≥ 1.0 cm by spiral CT scan

      • Lesions on chest x-ray allowed provided they are clearly defined and surrounded by aerated lung
    • Clincal lesions only considered measurable when they are superficial (e.g., skin nodules or palpable lymph nodes)
    • Target lesion must not have been exposed to prior radiotherapy unless disease has progressed since completion of radiotherapy
    • The following are not considered measurable disease:

      • Bone lesions
      • Leptomeningeal disease
      • Ascites
      • Pleural or pericardial effusion
      • Inflammatory breast disease
      • Lymphangitis cutis or pulmonis
      • Abdominal masses that are not confirmed and followed by imaging techniques
      • Cystic lesions
  • No HER2/neu-positive tumors by immunohistochemistry or amplified fluorescence in situ hybridization unless disease has progressed after trastuzumab (Herceptin®)-containing therapy alone or with antiestrogen hormonal therapy for metastatic disease OR trastuzumab is contraindicated
  • Prior breast cancer allowed
  • No prior or active brain metastases
  • Hormone receptor status:

    • Not specified

PATIENT CHARACTERISTICS:

Age

  • 18 and over

Sex

  • Male or female

Menopausal status

  • Not specified

Performance status

  • ECOG 0-1

Life expectancy

  • At least 3 months

Hematopoietic

  • Absolute neutrophil count ≥ 1,500/mm^3
  • Platelet count ≥ 100,000/mm^3
  • Hemoglobin ≥ 8.0 g/dL
  • No bleeding diathesis or uncontrolled coagulopathy

Hepatic

  • Bilirubin normal
  • Meets 1 of the following criteria:

    • AST and ALT normal AND alkaline phosphatase ≤ 5 times upper limit of normal (ULN)
    • AST and ALT ≤ 1.5 times ULN AND alkaline phosphatase ≤ 2.5 times ULN
    • AST and ALT ≤ 5 times ULN AND alkaline phosphatase normal

Renal

  • Creatinine clearance ≥ 30 mL/min
  • No proteinuria OR
  • Protein < 1 g by 24-hour urine collection
  • No nephrotic syndrome

Cardiovascular

  • No uncontrolled hypertension (i.e., blood pressure > 160/90 mm Hg on ≥ 2 different observations ≥ 5 minutes apart)

    • Blood pressure < 140/90 mm Hg on ≥ 3 different observations over ≥ 14 days, for patients who recently began or adjusted anti-hypertensive medication
  • No atrial or venous thrombosis within the past month
  • No clinically significant heart disease, including any of the following:

    • Congestive heart failure
    • Symptomatic coronary artery disease
    • Uncontrolled cardiac arrhythmias
    • Unstable angina
  • No myocardial infarction within the past 12 months
  • No history of cerebrovascular accident

Pulmonary

  • No hemoptysis within the past 6 months

Gastrointestinal

  • No lack of physical integrity of the upper gastrointestinal tract
  • No malabsorption syndrome
  • Able to receive oral medication

Other

  • No other stage III or IV invasive malignancy requiring treatment within the past 5 years
  • No pre-existing peripheral neuropathy > grade 1
  • No history of allergy or hypersensitivity to study drugs, agents that are chemically similar to study drugs, or drugs that contain polysorbate 80
  • No prior severe reaction to fluoropyrimidines
  • No known hypersensitivity to fluorouracil
  • No known dihydropyrimidine dehydrogenase deficiency
  • No active infection
  • No significant medical condition that would preclude study participation
  • Not pregnant or nursing
  • Negative pregnancy test
  • Fertile patients must use effective contraception during and for 30 days after study participation

PRIOR CONCURRENT THERAPY:

Biologic therapy

  • See Disease Characteristics
  • No other concurrent biologic therapy

Chemotherapy

  • Prior adjuvant or neoadjuvant chemotherapy allowed for primary disease
  • No prior chemotherapy for metastatic disease
  • More than 4 weeks since prior cytotoxic chemotherapy
  • More than 6 months since prior taxanes (e.g., docetaxel or paclitaxel)
  • No other concurrent chemotherapy

Endocrine therapy

  • See Disease Characteristics
  • Prior antiestrogen hormonal therapy allowed in the adjuvant or metastatic setting

Radiotherapy

  • See Disease Characteristics
  • More than 4 weeks since prior radiotherapy to a target lesion

    • Prior single-dose palliative radiotherapy allowed within the past 4 weeks
  • No concurrent radiotherapy

Surgery

  • More than 4 weeks since prior major surgery

Other

  • More than 2 weeks since prior aspirin, anticoagulants, or thrombolytic agents

    • Concurrent low-dose warfarin (1 mg/day) to maintain patency of vascular access device allowed
  • More than 4 weeks since prior investigational agents
  • No concurrent aspirin, anticoagulants, or thrombolytic agents
  • No concurrent participation in another clinical trial involving investigational agents or procedures

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: docetaxel + bevacizumab + capecitabine

Patients receive docetaxel IV over 1 hour and bevacizumab IV over 30-90 minutes on day 1. Patients also receive oral capecitabine twice daily on days 1-14. Courses repeat every 21 days in the absence of disease progression or unacceptable toxicity. Patients achieving a complete response (CR) receive at least 2 additional courses beyond CR.

Patients are followed every 3 months for 1 year, every 6 months for 1 year, and then annually for 3 years.

¿Qué mide el estudio?

Medidas de resultado primarias

Medida de resultado
Periodo de tiempo
Confirmed tumor response (complete or partial) rate as measured by RECIST
Periodo de tiempo: Up to 5 years
Up to 5 years

Medidas de resultado secundarias

Medida de resultado
Periodo de tiempo
Supervivencia libre de progresión
Periodo de tiempo: Hasta 5 años
Hasta 5 años
Sobrevivencia promedio
Periodo de tiempo: Hasta 5 años
Hasta 5 años

Colaboradores e Investigadores

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

Publicaciones y enlaces útiles

La persona responsable de ingresar información sobre el estudio proporciona voluntariamente estas publicaciones. Estos pueden ser sobre cualquier cosa relacionada con el estudio.

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 diciembre de 2004

Finalización primaria (Actual)

1 de agosto de 2006

Finalización del estudio (Actual)

1 de diciembre de 2010

Fechas de registro del estudio

Enviado por primera vez

4 de agosto de 2004

Primero enviado que cumplió con los criterios de control de calidad

4 de agosto de 2004

Publicado por primera vez (Estimar)

5 de agosto de 2004

Actualizaciones de registros de estudio

Última actualización publicada (Estimar)

7 de diciembre de 2016

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

5 de diciembre de 2016

Última verificación

1 de diciembre de 2016

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. .

Suscribir