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Liver Cancer clinical trials

View clinical trials related to Liver Cancer.

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NCT ID: NCT01075399 Completed - Lung Cancer Clinical Trials

Study of [F 18]HX4 Positron Emission Tomography (PET) as a Tool to Detect Hypoxia in Tumors

HX4-200
Start date: February 2010
Phase: Phase 2
Study type: Interventional

This pilot phase II study is designed as a test and retest study to investigate [F 18]HX4 as a reliable non-invasive PET imaging marker for detection of tumor hypoxia regions and to establish a threshold for [F 18]HX4 uptake in the tumor. The study will evaluate the relationship between hypoxia biomarkers (HIF1α and CA-IX) by immunohistochemistry (IHC) and tumor uptake of [F 18]HX4 by PET imaging.

NCT ID: NCT01075113 Completed - Liver Cancer Clinical Trials

Sorafenib and Vorinostat in Treating Patients With Advanced Liver Cancer

Start date: August 10, 2010
Phase: Phase 1
Study type: Interventional

This phase I trial is studying the side effects and best dose of vorinostat when given together with sorafenib tosylate in treating patients with advanced liver cancer. Sorafenib tosylate and vorinostat may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth or by blocking blood flow to the tumor.

NCT ID: NCT01071434 Terminated - Lung Cancer Clinical Trials

Feasibility of Using Real-time Cine-MRI for Treating Moving & Deforming Tumors

Start date: February 2009
Phase: N/A
Study type: Observational

This study aims to investigate and optimize imaging sequences and parameters of rapid real-time MRI in order to obtain adequate guidance for accurately and precisely delivering radiation to moving abdominal and thoracic tumors.

NCT ID: NCT01061840 Completed - Clinical trials for Non Small Cell Lung Cancer

Trial of Bi-shRNA-furin and GMCSF Augmented Autologous Tumor Cell Vaccine for Advanced Cancer

Start date: December 2009
Phase: Phase 1
Study type: Interventional

Autologous Vigil™ vaccine expresses rhGMCSF and bi-shRNAfurin from the Vigil™ plasmid. The GMCSF protein is a potent stimulator of the immune system, recruiting immune effectors to the site of intradermal injection and promoting antigen presentation. The furin bifunctional shRNA blocks furin protein production at the post transcriptional and translational levels. This decrease in furin in turn decreases the conversion of the proforms TGFβ1 and TGFβ2 proteins. Also, reduced furin protein levels have a negative feedback inhibition on TGFβ1 and TGFβ2 gene expression, decreasing the levels of their mRNAs. The resulting decrease in TGFβ1 and TGFβ2 proteins reduces the local immunosuppression they cause and promotes tumor surface antigen and MHC protein display.

NCT ID: NCT01042041 Completed - Clinical trials for Hepatocellular Carcinoma

Sorafenib Tosylate and Chemoembolization in Treating Patients With Unresectable Liver Cancer

Start date: September 2009
Phase: Phase 1
Study type: Interventional

RATIONALE: Sorafenib tosylate may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth or by blocking blood flow to the tumor. Drugs used in chemotherapy work in different ways to stop the growth of cancer cells, either by killing the cells or by stopping them from dividing. Chemoembolization kills tumor cells by blocking the blood flow to the tumor and keeping chemotherapy drugs near the tumor. PURPOSE: This phase I trial is studying side effects and best dose of sorafenib tosylate when given together with chemoembolization in treating patients with unresectable liver cancer.

NCT ID: NCT01033695 Completed - Pancreatic Cancer Clinical Trials

Interobserver Agreement of Endoscopic Ultrasonography and Endoscopic Sonoelastography in the Evaluation of Lymph Nodes

Start date: January 2008
Phase: N/A
Study type: Observational

Endoscopic ultrasound (EUS) is an important part of the pre-treatment evaluation of patients with upper gastrointestinal tract cancer (esophageal, gastric, pancreatic and liver cancer). When planning the optimal therapy in patients with upper gastrointestinal malignancies it is essential to know the exact lymph node stage. Recently endoscopic sonoelastography(ES) has been added to conventional EUS examination and may provide complementary information to distinguish benign for malignant lymph nodes. The N-stage relates to the treatment choice and the prognosis, and it is therefore of particular interest to know the interobserver agreement in operator dependent techniques. This study evaluate the interobserver agreement of EUS and ES evaluation og lymph nodes.

NCT ID: NCT01033240 Completed - Liver Cancer Clinical Trials

CS1008- in Combination With Sorafenib Compared to Sorafenib Alone in Subjects With Advanced Liver Cancer

Start date: July 9, 2010
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the safety and efficacy of CS-1008 in combination with sorafenib to sorafenib alone for treating liver cancer. Approximately 160 participants will take part in this study at approximately 22 sites (4 in the US, 8 in Japan, and 10 in Asia).

NCT ID: NCT01030757 Terminated - Liver Cancer Clinical Trials

Study of Stereotactic Body Radiation Therapy Using Tomotherapy for Metastatic Tumors to the Liver

Start date: June 2009
Phase: Phase 2
Study type: Interventional

The purpose of this study is to determine the response of liver tumors to radiation therapy using Tomotherapy.

NCT ID: NCT01024530 Recruiting - Clinical trials for Hepatocellular Carcinoma

Phase II/III Trial of Hepatocellular Carcinoma Patients Treated by ex Vivo Expanded Autologous Immune Killer Cells as the Adjunct Therapy

Start date: May 2009
Phase: Phase 2/Phase 3
Study type: Interventional

The purpose of this study is to evaluate the efficacy of ex vivo expanded autologous immune killer cells in treating hepatocellular carcinoma patients in: 1. Reduction of tumor size 2. Reducing the relapse rate: Reducing the frequency of TACE treatment by IKC injections.

NCT ID: NCT01020812 Terminated - Clinical trials for Carcinoma, Hepatocellular

Combination SBRT With TACE for Unresectable Hepatocellular Carcinoma

Start date: September 2009
Phase: Phase 1/Phase 2
Study type: Interventional

To determine the efficacy and toxicity of TACE combined with SBRT