- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02015676
A Study of Herceptin (Trastuzumab) in Combination Chemotherapy in Patients With Metastatic or Locally Advanced Breast Cancer
26 de febrero de 2015 actualizado por: Hoffmann-La Roche
'A Study of the Effect of First Line Treatment With Paclitaxel and Myocet in Combination With Herceptin on Overall Tumor Response in Patients With Metastatic or Locally Advanced Breast Cancer and HER2 Overexpression.'
This study will define an optimal chemotherapy dose regimen of Myocet in combination with paclitaxel and intravenous Herceptin and will evaluate the efficacy and safety of this dose regimen in patients with metastatic or locally advanced breast cancer and HER2 overexpression.
The anticipated time on study treatment is 3-12 months.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Actual)
69
Fase
- Fase 2
- 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
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Madrid, España, 28027
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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 a 70 años (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Femenino
Descripción
Inclusion Criteria:
- women 18-70 years of age;
- metastatic or locally advanced breast cancer;
- HER2 overexpression;
- >= 1 measurable lesion.
Exclusion Criteria:
- prior treatment for advanced breast cancer;
- prior treatment with Herceptin;
- bone or central nervous system metastasis as the only site of disease;
- history of another malignancy (except basal cell skin cancer and cancer in situ of the uterine cervix, and contralateral breast cancer) within 5 years of study.
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: No aleatorizado
- Modelo Intervencionista: Asignación de un solo grupo
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
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Experimental: Trastuzumab, Myocet, Paclitaxel; Phase I
Participants received an initial loading dose of trastuzumab 4 milligrams per kilogram (mg/kg), intravenously (IV), over 1.5 hours during Week 1, followed by 2 mg/kg, IV, over 30 minutes once per week from Week 2 to Week 52 or until disease progression.
Participants also received myocet, 40 mg/ square meter (m^2), IV, every 3 weeks, from Week 1; if no dose limiting toxicity (DLT) was observed in greater than or equal to (≥) two-thirds (2/3) of cohort for 2 treatment cycles, the dose was increased to 50 mg/m^2, IV, and continued for 6 cycles.
Participants also received paclitaxel 60 mg/ m^2, IV, once per week, from Week 19; if no DLT was observed in ≥ 2/3 of cohort for 2 treatment cycles, the dose was increased to 70 mg/m^2, IV, and subsequently 80 mg/m^2, IV, and continued until disease progression.
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Initial loading does of 4 mg/kg IV, followed by 2 mg/kg IV weekly, until disease progression
Otros nombres:
60 mg/m^2 IV weekly; dose increased to 70 mg/m^2, and subsequently 80 mg/m^2, after 2 treatment cycles with no evidence of DLT until disease progression
40 mg/m^2 IV weekly; dose increased to 50 mg/m^2 IV after 2 treatment cycles with no evidence of DLT for 6 cycles
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Experimental: Trastuzumab, Myocet, Paclitaxel; Phase II
Participants received an initial loading dose of trastuzumab 4 mg/kg, IV, over 1.5 hours during Week 1, followed by 2 mg/kg, IV, over 30 minutes once per week from Week 2 to Week 52 or until disease progression.
Participants also received myocet, 50 mg/m^2, IV, every 3 weeks, from Week 1 for 6 cycles.
Participants also received paclitaxel 80 mg/m^2, IV, once per week, from Week 19 until disease progression.
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Initial loading does of 4 mg/kg IV, followed by 2 mg/kg IV weekly, until disease progression
Otros nombres:
60 mg/m^2 IV weekly; dose increased to 70 mg/m^2, and subsequently 80 mg/m^2, after 2 treatment cycles with no evidence of DLT until disease progression
40 mg/m^2 IV weekly; dose increased to 50 mg/m^2 IV after 2 treatment cycles with no evidence of DLT for 6 cycles
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Percentage of Participants Achieving Complete Response (CR) or Partial Response (PR) According to World Health Organization (WHO) Handbook for Reporting Results of Cancer Treatment
Periodo de tiempo: Baseline (BL), Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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For measurable disease, CR was defined as the disappearance of all clinically detectable disease determined by 2 observations not less than 4 weeks apart; and PR was defined as a 50 percent (%) decrease in the sum of the products of the 2 greatest diameters of all measurable lesions by 2 observations not less than 4 weeks apart, and no appearance of new lesions or progression of any lesion.
For immeasurable disease, CR was defined as the complete disappearance of all known disease for at least 4 weeks; and PR was defined as an estimated decrease in tumor size of 50% or more for at least 4 weeks.
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Baseline (BL), Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Time to Disease Progression - Percentage of Participants With an Event
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Disease progression was defined as the time from the start of treatment to the date of the first recorded incident of disease progression, or the date of death due any cause.
For measurable disease, disease progression was defined as a ≥25% increase in the sum of the products of diameters of 1 or more measurable lesions with a minimal area of greater than (>)2 square centimeters (cm^2), or the appearance of new lesions; and for malignant lesions with a minimal area of 2 cm^2, an increase of ≥1 cm^2.
For immeasurable disease, disease progression was defined as the appearance of any new lesion not previously identified or an estimated increase of ≥50% in existent lesions.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Time to Disease Progression
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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The median time, in months, from the start of treatment to disease progression event.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Time to Treatment Response - Percentage of Participants With an Event
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Treatment response was defined as the time from the start of treatment to the date of recorded CR or PR of measurable disease.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Time to Treatment Response
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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The median time, in months, from the start of treatment to treatment response event.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Duration of Response - Percentage of Participants With an Event
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Duration of response was defined as the time from date CR was first recorded to the date progressive disease (PD) was first noted.
For measurable disease, PD was defined as a ≥25% increase in the sum of the products of diameters of 1 or more measurable lesions with a minimal area of >2 cm^2, or the appearance of new lesions; and for malignant lesions with a minimal area of 2 cm^2, an increase of ≥1 cm^2.
For immeasurable disease, PD was defined as the appearance of any new lesion not previously identified or an estimated increase of ≥50% in existent lesions.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Duration of Response
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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The median time, in months, from enrollment to duration of response event to Week 52.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Time to Therapy Failure - Percentage of Participants With an Event
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Therapy failure was defined as the date of the start of therapy to the date of withdrawal due to adverse events, progressive disease/insufficient therapeutic response, death, failure to return, or refusal of treatment/lack of cooperation/withdrawal of consent.
Participants were censored at the last dose of treatment if no event was recorded.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Time to Therapy Failure
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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The median time, in months, from treatment start to therapy failure event.
Participants were censored at the last date of treatment if no event was recorded.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Overall Survival (OS) - Percentage of Participants With an Event
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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OS was defined as the time from the date of the start of treatment to the date of death or the last date the participant was known to be alive.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Overall Survival
Periodo de tiempo: BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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The time, in months, from the start of treatment to OS event.
The mean survival time and it's standard error were underestimated because the largest observation was censored and the estimation was restricted to the largest event time.
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BL, Weeks 7, 13, 19, every 8 weeks thereafter until end of study (for up to 3 years)
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Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
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 julio de 2001
Finalización primaria (Actual)
1 de septiembre de 2009
Finalización del estudio (Actual)
1 de septiembre de 2009
Fechas de registro del estudio
Enviado por primera vez
3 de diciembre de 2013
Primero enviado que cumplió con los criterios de control de calidad
13 de diciembre de 2013
Publicado por primera vez (Estimar)
19 de diciembre de 2013
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
12 de marzo de 2015
Última actualización enviada que cumplió con los criterios de control de calidad
26 de febrero de 2015
Última verificación
1 de febrero de 2015
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
- Enfermedades de la piel
- Neoplasias
- Neoplasias por sitio
- Enfermedades de los senos
- Neoplasias de mama
- Mecanismos moleculares de acción farmacológica
- Agentes antineoplásicos
- Moduladores de tubulina
- Agentes antimitóticos
- Moduladores de mitosis
- Agentes antineoplásicos, fitogénicos
- Agentes antineoplásicos inmunológicos
- Paclitaxel
- Trastuzumab
Otros números de identificación del estudio
- M77035
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. .