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Liver Neoplasms clinical trials

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NCT ID: NCT02471313 Completed - Clinical trials for Hepatocellular Carcinoma

Integrated Imaging Strategy to Phenotype Progression of Liver Tumors During and After Chemoembolization

Start date: June 12, 2015
Phase: Phase 2
Study type: Interventional

Background: - Treatment for liver cancer can include surgery, transplant, and chemotherapy. It can also include other minimally invasive tumor treatments such as transarterial chemoembolization (TACE). TACE treatment for liver cancer helps control the cancer but is not considered a cure. Researchers want to learn more about the effects of TACE on liver tumors and surrounding tissue. To do this, they will use a positive emission test (PET) and a radioactive tracer called [18F] FMISO. Objectives: - To see if [18F] FMISO is useful for evaluating what happens to liver tumors and surrounding tissue after TACE. Eligibility: - People age 18 and older with liver cancer who have been approved to have TACE. Design: - Participants will meet with a study researcher to see if they can take part in the study. - Participants will have TACE under a separate NCI protocol or at a hospital other than the NIH Clinical Center. - Before and after TACE, participants will have a CT and MRI of the abdomen. For these scans, they will lie in a machine that takes pictures of their body. They will also have blood tests and a physical exam. - The [18F] FMISO imaging study will be performed at NIH only. - Participants will have an intravenous catheter placed in their arm (if they do not have one). The [18F] FMISO tracer will be injected. - Participants will have PET-CT scans. Each scan will take about 30 minutes. - Some participants will also have [18F] FMISO and PET-CT scans before TACE. - As part of standard care for TACE, participants will have CT and MRI scans at regular intervals. This will evaluate tumor response.

NCT ID: NCT02465892 Completed - Breast Cancer Clinical Trials

Pillars4Life Trial

Pillars4Life
Start date: May 2015
Phase: N/A
Study type: Interventional

This study aims to explore whether cancer patients can benefit from completing the Pillars4Life online coping program. This randomized control trial will have half its subject completing the program and the other half receiving standard care in order to measure whether the program is beneficial in dealing with stress, anxiety, and particularly chronic pain that often accompany a cancer diagnosis.

NCT ID: NCT02461966 Completed - Liver Cancer Clinical Trials

Evaluation of the Role of Aflatoxin as an Environmental Risk Factor Attributable to Liver Cancer in Nile Delta

Start date: June 2014
Phase: N/A
Study type: Interventional

Hepatocellular carcinoma is multifactorial in etiology and complex in pathogenesis, the blend of risk factors differs in different parts of the world, and this may explain in part the diverse biologic characteristics of HCC in different populations . Exposure to aflatoxin is an additional risk factor for the development of HCC, through damage of DNA in liver cells and mutation in p53 tumor suppressor gene . A previous study showed that aflatoxin B1 has a considerable role in the development of HCC among Egyptians . Clinical studies have shown that AFB1 selectively targets at the third base position of codon 249 of the human p53 gene, a known mutational hotspot in human hepatocellular carcinoma (HCC) . A significant association between aflatoxin exposure and HCC has been reported in hyperendemic areas . A synergistic interaction between AFB1 exposure and viral hepatitis B (HBV) infection on HCC risk has been reported in several epidemiologic studies. Aflatoxin exposure may be associated with advanced liver disease in chronic hepatitis C (HCV) patients. Levels of AFB1-albumin/albumin were significantly related to ultrasono-graphic hepatic parenchyma scores in anti-HCV-positive subjects .

NCT ID: NCT02456285 Completed - Clinical trials for Colorectal Neoplasms

Colorectal Cancer With Liver-limited Synchronous Metastases: an Inception Cohort Study of Standardised Care Pathways

CoSMIC
Start date: May 20, 2015
Phase:
Study type: Observational

Background When first diagnosed, colorectal cancer has already metastasized in about 20% of patients to the liver or further (termed synchronous disease). For patients with metastatic disease limited to the liver, major surgery to resect both the primary colorectal cancer and the liver metastasis provides 5-year survival rates of 25-40%. Conventional surgery removes the colorectal primary first, followed by adjuvant chemotherapy, and then resection of the liver metastasis. Surgical advances make synchronous resection (removing both primary and liver metastasis together) and liver-first resection possible. Currently, there is no conclusive evidence to show which approach improves morbidity or survival, and therefore there is no optimum clinical pathway. Treatment is decided at multidisciplinary team (MDT) meetings and is dependent on multiple factors: cancer staging, patient health and preferences, and clinical experience. Methods "Colorectal cancer with Synchronous liver-limited hepatic Metastasis: an Inception Cohort (CoSMIC)", will consent and recruit patients with a new diagnosis of synchronous colorectal cancer limited to the liver. Patients will be recruited at Manchester Royal Infirmary (a National Health Service (NHS) regional cancer-network approved Hepato-pancreato-biliary specialist centers over 2 years using standardized data collection. The sequence of treatment received by each patient, and factors influencing treatment decisions, will be recorded and evaluated against European Society of Medical Oncology guidelines. The effect of surgery on patient quality of life, morbidity, mortality and the long-term outcome will be measured and compared for different treatment sequences adjusted for prognostic factors. Anticipated Outputs and Value of Findings Direct comparison of conventional and new surgical sequences will be explored. Patient engagement, use of standardised recording, identifying common clinical patterns and decision making, and understanding sources of variation are essential steps to develop a definite randomized control trial to resolve the optimal clinical pathway.

NCT ID: NCT02454686 Completed - Liver Neoplasms Clinical Trials

Fibroscan Predicts Complications After Hepatectomy

Fibroscan
Start date: February 2012
Phase: N/A
Study type: Observational

Most of the postoperative complications that may occur after hepatectomy are related to the underlying liver background, and the common preoperative tests do not completely predict such complications. Transient elastography by Fibroscan is used to calculate the stiffness and the steatosis of the liver, and it may be also used to predict postoperative complications after hepatectomy

NCT ID: NCT02449109 Completed - Liver Cancer Clinical Trials

Nano Drug Interventional Therapy Using Digital Subtraction Angiography(DSA) for Liver Carcinoma

Start date: May 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of nano drug(Gemzar® mix with Compound Glycyrrhizin Injection) interventional therapy using digital subtraction angiography(DSA) for liver cancer.

NCT ID: NCT02447263 Completed - Liver Cancer Clinical Trials

HepaSphere Interventional Therapy Using Digital Subtraction Angiography(DSA) for Liver Cancer

Start date: May 2015
Phase: Phase 1/Phase 2
Study type: Interventional

The purpose of this study is to evaluate the safety and efficacy of HepaSphere interventional therapy using digital subtraction angiography(DSA) for liver cancer.

NCT ID: NCT02425735 Completed - Liver Cancer Clinical Trials

Safety and Efficiency of γδ T Cell Against Hepatocellular Liver Cancer

Start date: April 2015
Phase: Phase 1/Phase 2
Study type: Interventional

In this study, effects of γδT cells on human hepatocellular liver cancer in combination with tumor reducing surgery, for example cryosurgery going to be investigated.

NCT ID: NCT02424955 Completed - Clinical trials for Hepatocellular Carcinoma

Feasibility 3D Perfusion Ultrasound for Liver Cancer SABR Planning and Response Evaluation

Start date: November 18, 2014
Phase: N/A
Study type: Interventional

The purpose of this study is to prospectively analyze the value of 3D ultrasound perfusion imaging for treatment planning, the prediction of therapy success, and to monitor the treatment response in patients with a primary or metastatic liver tumor undergoing radiation treatment.

NCT ID: NCT02416466 Completed - Liver Metastases Clinical Trials

CAR-T Hepatic Artery Infusions and Sir-Spheres for Liver Metastases

HITM-SIR
Start date: April 2015
Phase: Phase 1
Study type: Interventional

This is an open label fixed dose phase Ib of anti-CEA CAR-T cells hepatic artery infusions and yttrium-90 SIR-Spheres in patients with CEA-expressing liver metastases.