- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT00609804
Sorafenib and Erlotinib or Sorafenib Alone in Advanced Non-Small Cell Lung Cancer Progressing on Erlotinib
10 de marzo de 2016 actualizado por: SCRI Development Innovations, LLC
Randomized Phase II Trial of Sorafenib and Erlotinib or Sorafenib Alone in Patients With Advanced Non-Small Cell Lung Cancer Progressing on Erlotinib
This is a randomized, open-label, multi-center, Phase II study of treatment of patients with advanced NSCLC who have progressed on erlotinib with the combination of sorafenib and erlotinib or sorafenib alone.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Actual)
53
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
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Florida
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Fort Myers, Florida, Estados Unidos, 33901
- Florida Cancer Specialists
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Georgia
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Gainesville, Georgia, Estados Unidos, 30501
- Northeast Georgia Medical Center
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Marietta, Georgia, Estados Unidos, 30060
- Wellstar Cancer Research
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Indiana
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Terre Haute, Indiana, Estados Unidos, 47802
- Providence Medical Group
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Kentucky
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Louisville, Kentucky, Estados Unidos, 40207
- Norton Cancer Institute
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Louisiana
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Baton Rouge, Louisiana, Estados Unidos, 70806
- Hematology Oncology Clinic, LLP
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Maryland
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Bethesda, Maryland, Estados Unidos, 20817
- Center for Cancer and Blood Disorders
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Bethesda, Maryland, Estados Unidos, 20817
- National Capital Clinical Research Consortium
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Mississippi
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Jackson, Mississippi, Estados Unidos, 39202
- Jackson Oncology Associates
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Missouri
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Chesterfield, Missouri, Estados Unidos, 63017
- St. Louis Cancer Care
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Kansas City, Missouri, Estados Unidos, 64132
- Research Medical Center
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Nebraska
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Omaha, Nebraska, Estados Unidos, 68114
- Nebraska Methodist Cancer Center
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New Jersey
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Morristown, New Jersey, Estados Unidos, 07960
- Hematology-Oncology Associates of Northern NJ
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Tennessee
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Chattanooga, Tennessee, Estados Unidos, 37404
- Chattanooga Oncology Hematology Associates
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Chattanooga, Tennessee, Estados Unidos, 37404
- Associates in Hematology Oncology
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Nashville, Tennessee, Estados Unidos, 37023
- Tennessee Oncology, PLLC
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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 y mayores (Adulto, Adulto Mayor)
Acepta Voluntarios Saludables
No
Géneros elegibles para el estudio
Todos
Descripción
Inclusion Criteria:
- Histologically confirmed stage IIIB/IV or relapsed non-small cell lung carcinoma (squamous carcinoma, adenocarcinoma, or large cell carcinoma). Patients with mixed tumors with small-cell elements are ineligible.
- Patients with no more than 2 prior lines of therapy, with the latest of those therapies being single-agent erlotinib.
- Evidence of progressive disease on erlotinib as assessed by the treating physician. Erlotinib must be the last treatment for NSCLC prior to enrollment into this study. Patients may be on erlotinib until enrollment. If erlotinib has already been stopped, the period of time off Erlotinib cannot exceed 14 days prior to study enrollment.
- Patients must have experienced a clinical benefit (complete response [CR], partial response [PR], or stable disease [SD]) from prior therapy with erlotinib for a period of 8 weeks.
- Patient must have one measurable lesion measuring at least 10 mm in the longest diameter (LD) by spiral computed tomography (CT), or 20 mm with conventional techniques according to the Response Evaluation Criteria in Solid Tumors (RECIST).
- Recovery from any toxic effects of erlotinib to ≤ grade 1 per the National Cancer Institute (NCI) Common Terminology Criteria for Adverse Events (CTCAE).
- Completion of palliative radiation therapy prior to the start of study treatment. Previously irradiated lesions in the advanced setting cannot be included as target lesions unless clear tumor progression has been observed following the completion of radiation therapy.
- Eastern Cooperative Oncology Group (ECOG) performance status of 0, 1, or 2.
- Absolute neutrophil count (ANC) >=1,500 and platelets >=75,000 (within 7 days prior to initial study treatment).
- Hemoglobin >=9 g/dL (within 7 days prior to initial treatment).
- International normalized ratio (INR) <=1.5 or prothrombin time (PT)/partial thromboplastin time (PTT) within normal limits (WNL) of the institution if not on anticoagulation therapy. Patients receiving anti-coagulation treatment with an agent such as warfarin or heparin may be allowed to participate with the therapeutic range established prior to study treatment initiation.
- Serum creatinine <=1.5 x institutional upper limit of normal (ULN) within 7 days prior to initial study treatment. If the absolute value is greater than 2mg/dL, the creatinine clearance, calculated according to the Cockroft-Gault formula, must be >=45 mL/min to be eligible.
- Bilirubin <=1.5 x the ULN; transaminases <=3 x institutional ULN, except in known hepatic metastasis, wherein these may be >=5 x institutional ULN.
- Patients must be able to understand the nature of this study, give written informed consent, and comply with study requirements.
- Agreement of male patients (with partners of childbearing potential) and female patients of childbearing potential to use effective contraception to prevent pregnancy during treatment and for a minimum of 90 days thereafter. Additionally, women should not breastfeed during this time.
Exclusion Criteria:
- Past or current history of neoplasm other than the entry diagnosis, with the exception of treated non-melanoma skin cancer or carcinoma in situ of the cervix, or other cancers cured by local therapy alone, and a disease-free survival (DFS) >=3 years.
- Pregnancy or lactation. All females of child-bearing potential must have negative serum or urine pregnancy tests within 7 days prior to study treatment.
- Prior epithelial growth factor receptor (EGFR) inhibitors, with the exception of erlotinib, are not allowed. This includes both tyrosine kinase inhibitors (TKIs) and monoclonal antibodies. Prior vascular endothelial growth factor (VEGF) inhibitors, with the exception of bevacizumab, are not allowed.
Significant cardiac disease within 90 days of starting study treatment including:
- superior vena cava syndrome
- new onset angina
- congestive heart failure (CHF) > Class 2 per New York Heart Association (NYHA) classification
- arrhythmia
- valvular heart disease.
- Myocardial infarction within 6 months prior to initiation of study treatment
- Cardiomegaly on chest imaging or ventricular hypertrophy on electrocardiogram (ECG) unless the left ventricular ejection fraction (LVEF) is within normal range for the institution.
- Poorly controlled hypertension (defined as systolic blood pressure [BP] >150 mm Hg and/or diastolic BP >100 mm Hg on antihypertensive medications).
- Unstable angina (anginal symptoms at rest).
- Cardiac ventricular arrhythmias requiring anti-arrhythmic therapy.
- Presence of cardiac disease that, in the opinion of the investigator, increases the risk of ventricular arrhythmia.
- A serious active infection (> grade 2) at the time of treatment
- A serious underlying medical condition that would impair the ability of the patient to receive protocol treatment.
- Untreated brain metastases. Patients who have treated metastases >=4 weeks out (with surgery and/or radiation therapy) and no evidence of central nervous system (CNS) progression are eligible.
- Treatment with a non-approved or investigational drug within 28 days of initial study treatment.
- A major surgical procedure, open biopsy, or significant traumatic injury within 28 days of beginning treatment or anticipation of need for major surgery during the course of the study.
- Thrombolic or embolic events such as a stroke and transient ischemic attack (TIA) within the past 6 months.
- Any prior history of hypertensive crisis or hypertensive encephalopathy.
- Pulmonary hemorrhage/bleeding event >= grade 2 within 28 days of initial study treatment.
- Any other non-pulmonary hemorrhage/bleeding event >= grade 3 within 28 days of initial study treatment.
- Evidence or history of bleeding diathesis or coagulopathy.
- Serious non-healing wound, ulcer, or bone fracture.
- Use of St. John's Wort or rifampin (rifampicin).
- Known or suspected allergy/hypersensitivity to any agent given in the course of this trial.
- Any malabsorption problem.
- Any condition that impairs the patient's ability to swallow whole pills.
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 |
|---|---|
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Experimental: Sorafenib+Erlotinib
Sorafenib 400 mg twice daily by mouth Erlotinib 150 mg once daily by mouth
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Sorafenib 400 mg twice daily by mouth Study treatment will be given in cycles of 28 days.
Patients will be re-staged every 2 treatment cycles (every 8 weeks).
Patients with an objective response or stable disease will continue study treatment.
Patients will continue until disease progression or intolerable toxicity occurs.
Otros nombres:
Erlotinib 150 mg once daily by mouth
Otros nombres:
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Comparador activo: Sorafenib
Sorafenib 400 mg twice daily by mouth.
|
Sorafenib 400 mg twice daily by mouth Study treatment will be given in cycles of 28 days.
Patients will be re-staged every 2 treatment cycles (every 8 weeks).
Patients with an objective response or stable disease will continue study treatment.
Patients will continue until disease progression or intolerable toxicity occurs.
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Progression-free Survival (PFS)
Periodo de tiempo: 18 months
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The Length of Time, in Months, That Patients Were Alive From Their First Date of Protocol Treatment Until Worsening of Their Disease.
Progression is defined using Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0), as a 20% increase in the sum of the longest diameter of target lesions, or a measurable increase in a non-target lesion, or the appearance of new lesions.
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18 months
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
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Overall Response Rate
Periodo de tiempo: 18 months
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The Number of Patients Who Experience an Objective Benefit From Treatment.
Per Response Evaluation Criteria In Solid Tumors Criteria (RECIST v1.0) for target lesions and assessed by MRI or CT: Complete Response (CR), Disappearance of all target lesions; Partial Response (PR), >=30% decrease in the sum of the longest diameter of target lesions; Overall Response (OR) = CR + PR.
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18 months
|
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Number of Participants With Treatment-emergent Adverse Events as a Measure of Safety and Tolerability
Periodo de tiempo: 18 months
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Defined as the number of participants with treatment-emergent grade 3/4 adverse events utilizing the National Cancer Institute Common Technology Criteria for Adverse Events (NCI CTCAE) v3.0
|
18 months
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Patrocinador
Investigadores
- Silla de estudio: David Spigel, M.D., SCRI Development Innovations, LLC
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 marzo de 2008
Finalización primaria (Actual)
1 de mayo de 2012
Finalización del estudio (Actual)
1 de noviembre de 2014
Fechas de registro del estudio
Enviado por primera vez
24 de enero de 2008
Primero enviado que cumplió con los criterios de control de calidad
24 de enero de 2008
Publicado por primera vez (Estimar)
7 de febrero de 2008
Actualizaciones de registros de estudio
Última actualización publicada (Estimar)
8 de abril de 2016
Última actualización enviada que cumplió con los criterios de control de calidad
10 de marzo de 2016
Última verificación
1 de marzo de 2016
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
- Enfermedades de las vías respiratorias
- Neoplasias
- Enfermedades pulmonares
- Neoplasias por sitio
- Neoplasias de las vías respiratorias
- Neoplasias torácicas
- Carcinoma Broncogénico
- Neoplasias Bronquiales
- Neoplasias Pulmonares
- Carcinoma de pulmón de células no pequeñas
- Mecanismos moleculares de acción farmacológica
- Inhibidores de enzimas
- Agentes antineoplásicos
- Inhibidores de la proteína quinasa
- Clorhidrato de erlotinib
- Sorafenib
Otros números de identificación del estudio
- SCRI LUN 162
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. .