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The Utility of Positron Emission Tomography (PET) in Staging of Patients With Potentially Operable Carcinoma of the Thoracic Esophagus

0 criterios cumplidosConsulta de un vistazo cómo tu perfil cumple con cada criterio de elegibilidad.
Qué se está evaluando

conventional surgery

+ positron emission tomography

+ radionuclide imaging

ProcedimientoRadiaciónMedicamento
Quiénes están siendo reclutados

Carcinoma+11

+ Carcinoma de Células Escamosas

+ Enfermedades del Sistema Digestivo

A partir de 18 años
Ver todos los criterios de elegibilidad
Cómo está diseñado el estudio

Estudio Diagnóstico

Intervencional
Inicio del estudio: noviembre de 1999
Ver detalles del protocolo

Resumen

Patrocinador PrincipalAlliance for Clinical Trials in Oncology
Última actualización: 24 de enero de 2017
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Fecha de inicio: 1 de noviembre de 1999

Fecha en la que se inscribió al primer participante.

OBJECTIVES: Primary Objective: To evaluate whether FDG-PET imaging can detect lesions that would preclude surgery (esophagectomy) in patients found to be surgical candidates by standard imaging procedures. Secondary Objective: To use the collected data to generate hypotheses to be used in future studies, such as which types of previously undetected lesions FDG-PET imaging is best able to identify.

NCT00004867
Patrocinador PrincipalAlliance for Clinical Trials in Oncology
Última actualización: 24 de enero de 2017
Extraido de una base de datos validada por el gobierno.Reclamar como socio

Protocolo

Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.
Detalles del Diseño

Se reclutarán 235 pacientes

Número total de participantes que el ensayo clínico espera reclutar.

Estudio Diagnóstico

Los estudios diagnósticos se centran en mejorar como se detecta o confirma una enfermedad. Prueban nuevas herramientas o técnicas que podrían ofrecer diagnósticos más rápidos o precisos.



Elegibilidad

Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.
Condiciones
Criterios

Cualquier sexo

Sexo biológico de los participantes elegibles para inscribirse.

A partir de 18 años

Rango de edades de los participantes que pueden unirse al estudio.

Voluntarios sanos no permitidos

Indica si personas sanas, sin la condición que se estudia, pueden participar.

Condiciones

Patología

CarcinomaCarcinoma de Células EscamosasEnfermedades del Sistema DigestivoNeoplasias del sistema digestivoEnfermedades del esófagoEnfermedades GastrointestinalesNeoplasias GastrointestinalesNeoplasias de cabeza y cuelloNeoplasiasNeoplasias por tipo histológicoNeoplasias por SitioNeoplasias glandulares y epitelialesCarcinoma de células escamosas del esófagoNeoplasias Esofágicas

Criterios

Inclusion Criteria: Patient must be ≥ 18 years of age. Patient must have histologically confirmed squamous cell carcinoma or adenocarcinoma of the thoracic esophagus (greater than or equal to 20 cm from incisors) or gastroesophageal junction. (Pathology report must be submitted). Patient must be deemed medically fit for surgical staging procedures and esophagectomy following the thoracic surgeon's evaluation of general medical fitness. Patient's clinical staging data (clinical examination, laboratory tests, and standard radiological staging assessments) must be obtained within 60 days prior to registration and must suggest that the tumor is potentially resectable, including tumors staged T1-3, N0-1, M0. Patient must be able to tolerate FDG-PET scan (e.g., not claustrophobic and able to lie supine for 1.5 hrs). Female patient of childbearing potential must have a negative serum or urine pregnancy test within 72 hours prior to FDG-PET. NOTE: Pregnancy test is required to avoid unnecessary fetal radiation exposure and because the use of furosemide is contraindicated in pregnancy. Patient or the patient's legally acceptable representative must provide a signed and dated written informed consent prior to registration and any study related procedures. Patient must provide written authorization to allow the use and disclosure of their protected health information. NOTE: This may be obtained in either the study-specific informed consent or in a separate authorization form and must be obtained from the patient prior to study pre-registration. A cancer survivor is eligible provided that ALL of the following criteria are met and documented: the patient has undergone potentially curative therapy for all prior malignancies and there has been no evidence of any prior malignancies for at least five years (except for completely resected cervical or non-melanoma skin cancer) and the patient is deemed by their treating physician to be at low risk for recurrence from prior malignancies. Exclusion Criteria: Patient has proximal esophageal cancer (less than 20 cm from incisors) potentially requiring pharyngolaryngoesophagectomy. Patient has unresectable lesions (stage M1b, with biopsy confirmation of distant metastatic disease; or those with unresectable locoregional invasion, T4 Nx Mx). Patient has evidence of metastatic disease. NOTE: Obvious metastasis that is based on clinical evaluation includes any or all of the following: positive cytology of pleura, pericardium, or peritoneum; metastasis to brain, bone, lung, liver, or adrenals; positive biopsy or cytology of metastasis to supraclavicular lymph nodes; and involvement of the tracheobronchial tree (positive bronchoscopic biopsy or overt esophago-respiratory fistula). Patient has had a prior FDG-PET scan for evaluation of their esophageal cancer. Patient has uncontrolled diabetes mellitus, as evidenced by a fasting blood glucose value >200 mg/dL, within 12 hours of FDG-PET scan. Patient has received neoadjuvant chemotherapy and/or radiotherapy PRIOR to FDG-PET scan being performed.

Plan de Estudio

Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.
Grupos de Tratamiento
Objetivos del Estudio

Un solo grupo de intervención está designado en este estudio

0% de probabilidad de ser asignado al grupo placebo

Grupos de Tratamiento

Grupo I

Experimental
Patients receive fludeoxyglucose F 18 (FDG) IV followed 45-60 minutes later by positron emission tomography (PET) imaging. Confirmatory studies, such as biopsy or other imaging studies, are then conducted to confirm the FDG PET imaging results. Patients with no metastases identified by FDG PET imaging may undergo esophagectomy with or without neoadjuvant chemoradiotherapy within 1 month of evaluation. Patients are followed within 6 months after surgery.

Objetivos del Estudio

Objetivos Primarios

Objetivos Secundarios

Centros del Estudio

Estos son los hospitales, clínicas o centros de investigación donde se lleva a cabo el estudio. Puedes encontrar la ubicación más cercana a ti y su estado de reclutamiento.

Este estudio tiene 35 ubicaciones

Comprehensive Cancer Center at University of Alabama at Birmingham

Birmingham, United StatesAbrir Comprehensive Cancer Center at University of Alabama at Birmingham en Google Maps

Mobile Infirmary Medical Center

Mobile, United States

University of South Alabama Cancer Research Institute

Mobile, United States

Jonsson Comprehensive Cancer Center at UCLA

Los Angeles, United States
Completado35 Centros de Estudio