- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT01985958
A Pilot Study to Evaluate Radiotherapy-Induced Anti-Tumor Immunity in Metastatic Carcinoma of the Pancreas
A Pilot Study to Evaluate Radiotherapy-Induced Ant-Tumor Immunity in Metastatic Carcinoma of the Pancreas
Primary Objective: To estimate the rate at which radiotherapy to the primary or a metastatic lesion produces an immune response in patients with metastatic carcinoma of the pancreas.
Secondary Objectives: To characterize the kinetics of an immune response induced by radiotherapy. To characterize the dependency of the immune response on prior exposure to chemotherapy.
Descripción general del estudio
Estado
Intervención / Tratamiento
Tipo de estudio
Inscripción (Actual)
Fase
- No aplica
Contactos y Ubicaciones
Ubicaciones de estudio
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Pennsylvania
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Philadelphia, Pennsylvania, Estados Unidos, 19104
- Abramson Cancer Center of the University of Pennsylvania
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Criterios de participación
Criterio de elegibilidad
Edades elegibles para estudiar
Acepta Voluntarios Saludables
Géneros elegibles para el estudio
Descripción
Inclusion Criteria:
- Histological or cytological diagnosis of pancreatic carcinoma
- Patients ≥ 18 years of age
- Eastern Cooperative Oncology Group (ECOG) performance status 0,1,or 2
- Patients must have distant metastatic disease (stage 4)
- Satisfactory organ and bone marrow function as defined by: Absolute neutrophil count> 1,000/uL, Platelets > 75,000uL Hemoglobin > 9 Bilirubin ≤ 2.0x the institutional normal upper limit unless secondary to bile duct obstruction by tumor,
- Creatinine ≤ 1.5x the institutional normal upper limit
- Serum alanine aminotransferase (ALT) or aspartate aminotransferase (AST) ≤ 5x the institutional normal upper limit.
- A clinical recommendation for radiotherapy to the primary or a metastatic lesion had been made.
- Must be able to provide informed consent.
Exclusion Criteria:
- No prior radiation to the area planned for radiotherapy
- Active invasive cancer other than pancreatic adenocarcinoma. Non-melanoma skin cancer, superficial cervical or bladder cancer and prostate cancer with PSA level < 1.0 are not excluded.
- Known HIV, HCV and/or HBV positive (by patient report/medical record)
- Patients with ongoing or active infection
- Planned concurrent treatment with systemic high dose corticosteroids.
- Received an anticancer treatment (systemic therapy or radiation therapy)within 21 days prior to enrollment.
- Immunotherapy (e.g. monoclonal antibodies)within 21 days prior to enrollment.
- Immunosuppressive therapies (e.g. steroids, cyclosporine) are not permitted.
Plan de estudios
¿Cómo está diseñado el estudio?
Detalles de diseño
- Propósito principal: Diagnóstico
- Asignación: N / A
- Modelo Intervencionista: Asignación de un solo grupo
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
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Experimental: Single arm
In this trial, we will deliver low-dose (8Gy in a single fraction) radiotherapy (SBRT or any other acceptable delivery method as determined by the treating physician) for palliation of symptoms in patients in whom it is clinically indicated.
This dose is far lower than what has been used in the definitive settings described above.
This is a safe dose, and is entirely consistent with the dose range used for routine palliation.
Therefore, this trial does not involve an experimental intervention; the research aspect of this protocol is the evaluation of the immune response to clinically indicated palliative radiotherapy.
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¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Periodo de tiempo |
|---|---|
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Number of Participants With Adverse Events
Periodo de tiempo: One Year
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One Year
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Colaboradores e Investigadores
Investigadores
- Investigador principal: Edgar Ben-Josef, MD, Abramson Cancer Center of the University of Pennsylvania
Fechas de registro del estudio
Fechas importantes del estudio
Inicio del estudio
Finalización primaria (Actual)
Finalización del estudio (Actual)
Fechas de registro del estudio
Enviado por primera vez
Primero enviado que cumplió con los criterios de control de calidad
Publicado por primera vez (Estimar)
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
Última actualización enviada que cumplió con los criterios de control de calidad
Última verificación
Más información
Términos relacionados con este estudio
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- UPCC 14213
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