A Pilot Study on the Feasibility of Combined Chemoembolization and Adjuvant Systemic Hyperthermia for Palliative Treatment of Unresectable Hepatocellular Carcinoma(HCC)
TACE with Hyperthermia Treatment
Adenocarcinoma+8
+ Carcinoma
+ Enfermedades del Sistema Digestivo
Estudio de Tratamiento
Resumen
Fecha de inicio: 1 de marzo de 2013
Fecha en la que se inscribió al primer participante.Most patients with Hepatocellular carcinoma (HCC) are diagnosed at an intermediate and advanced stage when the tumors become unresectable. Transcatheter arterial chemoembolization (TACE) has been shown to be effective in prolongation of survival for patients with unresectable HCC and generally adopted as a standard palliative treatment option for patients with intermediate stage HCC. However, the therapeutic effect of TACE in terms of objective tumor response is variable and modest (27%-40%), indicating that there is actually much room for improvement in the treatment. In many cases, patients with intrahepatic HCC uncontrolled after TACE treatment may not be suitable for other treatment options because of their physical condition. For these patients, repeat TACE combined with adjuvant systemic hyperthermia may offer a chance of disease control.
Protocolo
Esta sección proporciona detalles del plan del estudio, incluyendo cómo está diseñado y qué se está evaluando.Se reclutarán 8 pacientes
Número total de participantes que el ensayo clínico espera reclutar.Estudio de Tratamiento
Elegibilidad
Los investigadores buscan pacientes que cumplan ciertos criterios, conocidos como criterios de elegibilidad: estado general de salud o tratamientos previos.Cualquier sexo
Sexo biológico de los participantes elegibles para inscribirse.De 18 a 75 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
Criterios
Inclusion Criteria: Patient factor Age between 18 and 75 Child-Pugh A cirrhosis Eastern Cooperative Oncology Group(ECOG) performance status Grade 2 or below No serious concurrent medical illness Prior treatment for HCC including surgery, local ablation, or transarterial treatments allowed Imaging evidence of poor intralesional treatment response or disease progression despite transarterial treatment Platelet count ≥ 50 10^9/L Tumor factor HCC diagnosed by typical enhancement patterns on cross sectional imaging or histology Unresectable and locally advanced disease without extra-hepatic disease Hypervascular lesions on CT Greatest dimension of the largest tumor ≤15cm Exclusion Criteria: Patient factor History of significant concurrent medical illness such as ischemic heart disease or heart failure Metallic body implants, not including dental fillings Serum creatinine level > 130 umol/L Presence of biliary obstruction not amenable to drainage Child-Pugh B or C cirrhosis Unable to give consent Evidence of impaired liver function History of hepatic encephalopathy Intractable ascites not controllable by medical therapy History of variceal bleeding within last 3 months Serum total bilirubin level >25 umol/L for the first 5 patients, serum total bilirubin level >35 umol/L for the second 5 patients Serum albumin level < 30g/L International normalized ratio(INR) >1.3 Tumor factor Presence of extrahepatic metastasis Infiltrative lesion Vascular invasion Hepatic artery thrombosis Partial or complete thrombosis of the main portal vein Tumor invasion of portal branch of contralateral lobe Hepatic vein tumor thrombus Significant arterioportal shunt Significant arteriovenous shunt Contraindication for hyperthermia Known brain metastasis Recent stroke or cerebral hemorrhage within last 6 months Poorly controlled epilepsy Poorly controlled cardiac arrhythmias Myocardial infarction within last 6 months Unstable angina within last 6 months Poorly controlled hypertension Poorly controlled diabetes History of malignant hyperthermia Photodermatosis Pregnancy Lactation Serious infection Grade 3 or above adverse event in serological total bilirubin or albumin according to Version 4.0 of National Cancer Institute Common Terminology Criteria for Adverse Events Elevation of serum alanine transaminase ≥ 10 times upper limit of normal
Plan de Estudio
Conoce todos los tratamientos administrados en este estudio, su descripción detallada y en qué consisten.Un solo grupo de intervención está designado en este estudio
0% de probabilidad de ser asignado al grupo placebo
Grupos de Tratamiento
Grupo I
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 2 ubicaciones
Department of Clinical Oncology, Prince of Wales Hospital, The Chinese University of Hong Kong
Hong Kong, Hong KongAbrir Department of Clinical Oncology, Prince of Wales Hospital, The Chinese University of Hong Kong en Google MapsDepartment of Imaging and Interventional Radiology, Prince of Wales Hospital, The Chinese University of Hong Kong
Hong Kong, Hong Kong