- ICH GCP
- Registro de ensayos clínicos de EE. UU.
- Ensayo clínico NCT02864316
Phase 2 Study of Nivolumab in Solid Tumors Induced by Prior Radiation Exposure
9 de agosto de 2019 actualizado por: Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
The purpose of this study is to determine whether Nivolumab is effective in the treatment of radiation-induced solid tumors.
Descripción general del estudio
Estado
Terminado
Condiciones
Intervención / Tratamiento
Tipo de estudio
Intervencionista
Inscripción (Actual)
6
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
-
-
Maryland
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Baltimore, Maryland, Estados Unidos, 21231
- Sidney Kimmel Cancer Center @ Johns Hopkins
-
-
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 metastatic or unresectable solid tumor which standard curative or palliative measures do not exist or are no longer effective. The primary site of the metastatic or unresectable tumor must have arisen within a previously irradiated site and be considered a radiation-induced tumor.
- Pre-treatment tumor specimen available. Patients with no available archived specimen must be willing to undergo a pre-treatment tumor biopsy.
- Measurable disease.
- Progressive disease on study entry.
- Received adjuvant or neoadjuvant chemotherapy and developed recurrent or metastatic disease within 6 months of completing therapy.
- Age >18 years.
- Eastern Cooperative Oncology Group (ECOG) performance status <2.
- Life expectancy of greater than 3 months.
- Adequate organ and marrow function as defined below:
- White Blood Cell >2,000/per microliter
- Absolute neutrophil count >1,500/per microliter
- Platelets >100,000/per microliter
- Hemoglobin ≥9.0 g/dL
- Total bilirubin ≤1.5 times the institutional upper limit of normal (ULN) (except subjects with Gilbert Syndrome, who can have total bilirubin < 3.0 mg/dL)
- Aspartate Aminotransferase(SGOT)/Alanine Aminotransferase (SGPT) <3 X institutional ULN
- Creatinine ≤1.5 X institutional ULN OR
- Creatinine clearance >40 mL/min for patients with creatinine Levels above institutional normal (calculated using the Cockcroft-Gault formula below)
- Female Creatinine Clearance = (140 - age in years) x weight in kg x 0.85 72 x serum creatinine in mg/dL
- Male Creatinine Clearance = (140 - age in years) x weight in kg x 1.00 72 x serum creatinine in mg/dL
- Women of childbearing potential (WOCBP) and men must agree to use adequate contraception prior to study entry and for the duration of study participation and up to 31 weeks after the last dose of nivolumab.
- Women of childbearing potential (WOCBP) must have a negative serum or urine pregnancy test within 24 hours prior to the start of nivolumab.
- Ability to understand and the willingness to sign a written informed consent document.
- Biopsiable disease at the time of enrollment as biopsies after progression are required for participation.
Exclusion Criteria:
- Any active, known or suspected autoimmune disease.
- Requiring continuous supplemental oxygen.
- Chemotherapy or radiotherapy within 2 weeks (6 weeks for nitrosoureas or mitomycin C) prior to entering the study or unresolved toxicity due to agents administered more than 2 weeks earlier.
- Uncontrolled brain metastases.
- History of allergic reactions attributed to compounds of similar chemical or biologic composition to nivolumab.
- Uncontrolled inter-current illness.
- Pregnant or currently breastfeeding.
- Receiving any other anticancer therapy.
- Prior therapy with anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, anti-CTLA- 4 antibody therapies, any other antibody or drug specifically targeting T-cell costimulation or checkpoint pathways.
- History of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).
- Positive test for hepatitis B virus surface antigen (HBV sAg) or hepatitis C virus ribonucleic acid (HCV antibody) indicating ongoing acute or chronic infection.
- Requiring systemic treatment with either corticosteroids (> 10 mg daily prednisone equivalent) or other immunosuppressive medications within 14 days of study drug administration.
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 paralela
- Enmascaramiento: Ninguno (etiqueta abierta)
Armas e Intervenciones
Grupo de participantes/brazo |
Intervención / Tratamiento |
|---|---|
|
Experimental: Radiation-Induced Metastatic Sarcoma
a flat dose of Nivolumab 240 mg will be administered intravenously every 2 weeks until disease progression.
|
Otros nombres:
|
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Experimental: Radiation-Induced Non-Sarcoma Metastatic Solid Tumors
a flat dose of Nivolumab 240 mg will be administered intravenously every 2 weeks until disease progression.
|
Otros nombres:
|
¿Qué mide el estudio?
Medidas de resultado primarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Best Objective Response Rate
Periodo de tiempo: Up to 24 weeks
|
Number of participants with response.
Response will be assessed at baseline (within 4 weeks prior to starting nivolumab) and then every 8 weeks while on Nivolumab, up to 24 weeks.
The best objective response will be assessed at 24 weeks.
Response will be defined based on RECIST 1.1 criteria where complete response (CR)= disappearance of all target lesions, partial response (PR) is =>30% decrease in sum of diameters of target lesions, progressive disease (PD) is >20% increase in sum of diameters of target lesions, stable disease (SD) is <30% decrease or <20% increase in sum of diameters of target lesions.
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Up to 24 weeks
|
Medidas de resultado secundarias
Medida de resultado |
Medida Descripción |
Periodo de tiempo |
|---|---|---|
|
Percentage of Patients Progression-free at 24 Weeks From the Time of Enrollment
Periodo de tiempo: 24 weeks
|
Disease status at 24 weeks will be compared to disease status at the time of enrollment, and response coded based on RECIST 1.1 criteria.
|
24 weeks
|
|
Progression-free Survival
Periodo de tiempo: Up to 22 months
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Number of participants alive without progression.
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Up to 22 months
|
|
Duration of Response
Periodo de tiempo: Up to 22 months
|
The duration of overall response is measured from the time measurement criteria are met for Complete Response or Partial Response (whichever is first recorded) until the first date that recurrent or progressive disease is objectively documented, accessed up to 3 years.
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Up to 22 months
|
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Number of Participants With Treatment-related Adverse Events
Periodo de tiempo: up to 100 days post-intervention
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Number of participants with treatment-related adverse events as defined by CTCAE 4.0 criteria.
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up to 100 days post-intervention
|
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Overall Survival
Periodo de tiempo: Up to 22 months
|
Overall survival was planned to be measured at 5 years post-intervention as the time from enrollment until death.
Instead, due to early termination for low accrual, the number of participants alive at the time of study termination is reported.
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Up to 22 months
|
Colaboradores e Investigadores
Aquí es donde encontrará personas y organizaciones involucradas en este estudio.
Colaboradores
Investigadores
- Investigador principal: Patrick Forde, MB, BCH, Sidney Kimmel Comprehensive Cancer Center at Johns Hopkins
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 2016
Finalización primaria (Actual)
1 de agosto de 2018
Finalización del estudio (Actual)
1 de septiembre de 2018
Fechas de registro del estudio
Enviado por primera vez
2 de agosto de 2016
Primero enviado que cumplió con los criterios de control de calidad
9 de agosto de 2016
Publicado por primera vez (Estimar)
12 de agosto de 2016
Actualizaciones de registros de estudio
Última actualización publicada (Actual)
28 de agosto de 2019
Última actualización enviada que cumplió con los criterios de control de calidad
9 de agosto de 2019
Última verificación
1 de agosto de 2019
Más información
Términos relacionados con este estudio
Palabras clave
Términos MeSH relevantes adicionales
Otros números de identificación del estudio
- J1695
- IRB00105682 (Otro identificador: JHMIRB)
Plan de datos de participantes individuales (IPD)
¿Planea compartir datos de participantes individuales (IPD)?
NO
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. .