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Hepatocellular Carcinoma clinical trials

View clinical trials related to Hepatocellular Carcinoma.

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NCT ID: NCT00162669 Recruiting - Clinical trials for Hepatocellular Carcinoma

Bevacizumab in Advanced Hepatocellular Carcinoma

Start date: May 2005
Phase: Phase 2
Study type: Interventional

Primary liver cancer (hepatocellular carcinoma) is the fifth most common malignant disorder, with an increasing incidence in Europe and the USA as a result of the high prevalence of hepatitis C. Most patients are not suitable for potentially curative treatment. There is no standard palliative treatment for patients with advanced hepatocellular carcinoma (HCC), as no drug has been demonstrated to be efficient in this disease in terms of survival. The use of anti-vascular agents might be a promising approach in view of the highly vascular nature of this tumor. The aim of this phase II trial is to evaluate the potential benefit of bevacizumab in terms of disease control rate, progression-free and overall survival in adult patients with advanced primary liver cancer. Bevacizumab is an angiogenesis inhibitor already successfully used in patients with colorectal and renal cancers.

NCT ID: NCT00155272 Recruiting - Clinical trials for Hepatocellular Carcinoma

Radiotherapy Plus Thalidomide in Locally Advanced Hepatocellular Carcinoma

Start date: March 2005
Phase: Phase 1/Phase 2
Study type: Interventional

This is a pilot study of concomitant radiotherapy and thalidomide for patients with locally advanced HCC.Besides toxicity and efficacy, mechanistic studies including dynamic contrast enhanced MRI and serum cytokines will be evaluated.

NCT ID: NCT00154817 Completed - Clinical trials for Hepatocellular Carcinoma

A Phase II Study of Radiotherapy for Locally Advanced Hepatocellular Carcinoma (HCC)

Start date: January 2002
Phase: Phase 2
Study type: Interventional

1. This is a phase II study of radiotherapy for patients with locally advanced HCC. 2. Patients whose tumor(s) are not suitable for other local treatment, such as surgery, trans-arterial chemoembolization (TAE), ethanol injection, or radiofrequency ablation. will be enrolled. 3. Radical radiotherapy will be started after pre-treatment evaluation. The total dose of RT will be 50Gy in 25 fractions to local tumor(s). 4. Dynamic contrast enhanced MRI and serum samples will be done at the following time points to assess the change in tumor perfusion: (1) before the start of thalidomide treatment; (2) 2weeks after radiotherapy begins; and (3) 1 month after radiotherapy completes. DCEMRI will then be done every 3 months until disease progression. 5. The study was designed to evaluate the response rate and tolerability of radical radiotherapy for locally advanced HCC. The sample size was determined by the expected incidence of grade 4 toxicity and response rate of radiotherapy for locally advanced HCC. Since the grade 4 toxicity of radiotherapy alone is 10%, the response rate is 60% we need at least 12 patients to evaluate for the treatment.

NCT ID: NCT00154544 Recruiting - Clinical trials for Hepatocellular Carcinoma

Searching for the Liver Cancer-Related Biomarkers

Start date: August 2004
Phase: Phase 1
Study type: Observational

Hepatocellular carcinoma (HCC) has been the leading cause of cancer death in Taiwan. About 6000-8000 people died of this cancer every year in Taiwan. Though regular sonographic examination can early detect small HCC and there are many therapeutic modalities for HCC, the therapeutic results remains unsatisfactory. Though Alpha-fetoprotein (AFP) and des-γ-carboxy prothrombin (DCP) are used as the tumor markers for diagnosis of HCCs, these two markers are not good enough for the early detection of small HCCs. To improve the survival, further investigations of the early diagnostic markers are still needed. In this current project, we applied the proteomic method to identify the HCC biomarkers.

NCT ID: NCT00154531 Recruiting - Clinical trials for Hepatocellular Carcinoma

Identification of Biomarkers Associated With Human Hepatocellular Carcinoma by SELDI

Start date: August 2004
Phase: N/A
Study type: Observational

Hepatocellular carcinoma (HCC) has been the leading cause of cancer death in Taiwan. Though Alpha-fetoprotein (AFP) and des-γ-carboxy prothrombin(DCP) are used as the tumor markers for diagnosis of HCCs. Thus, these two markers are not good enough for the early detection of small HCCs. To improve the survival, further investigations of the early diagnostic markers are still needed. SELDI is a proteomic profiling techniques in biomarker discovery. Its approach has been successfully used to identify biomarkers of various cancers, such as prostate cancer, bladder cancer, ovarian cancer, lung cancer, colon cancer, breast cancer and pancreatic cancer. In this current project we will apply the SELDI technique to identify the HCC biomarkers. Sera samples from the HCC patients and relevant controls will be collected. We hope that we can find the new HCC biomarkers. If biomarkers of HCC are identified, this can be used to clinical application for the possible early detection of HCCs.

NCT ID: NCT00151671 Terminated - Clinical trials for Hepatocellular Carcinoma

Effect of a Perioperative Oral Nutritional Supplementation on Patients Undergoing Hepatic Surgery for Liver Cancer

IMPACT
Start date: April 2003
Phase: Phase 2/Phase 3
Study type: Interventional

Cirrhotic patients undergoing hepatic resection have a mortality rate near 10%, and 30 to 70% of them develop severe complications. These failures are mainly due to hepatic insufficiency. Studies have already shown benefits of oral nutritional supplements in ORL, digestive, and cardiac surgery. We aimed to ascertain whether this nutritional, immune-enhancing supplementation, administered 7 days before and 3 days after surgery, could improve liver function and postoperative host defences in patients with liver cancer resection.

NCT ID: NCT00149565 Completed - Clinical trials for Hepatocellular Carcinoma

Phase Ⅲ Randomized Trial in Postoperative Hepatocellular Carcinoma

Start date: October 1997
Phase: Phase 3
Study type: Interventional

* OBJECTIVES 1. To investigate whether adjuvant IFN-α therapy can delay or reduce the 2-5 years recurrence rate in curatively resected HCC . 2. To examine whether adjuvant IFN-α therapy can prolong the disease-free survival in curatively resected HCC. 3. To determine the safety and tolerance of adjuvant IFN-α therapy in postoperative HCC with or without cirrhosis. 4. To investigate the change of activity of HBV and HCV in postoperative HCC patients with adjuvant IFN-α therapy. 5. To correlate the changes of viral status with the clinical outcome in post-operative HCC patients with adjuvant IFN-α therapy.

NCT ID: NCT00142467 Completed - Clinical trials for Hepatocellular Carcinoma

Gemcitabine, Oxaliplatin in Combination With Bevacizumab in Patients With Hepatocellular Carcinoma

Start date: April 2004
Phase: Phase 2
Study type: Interventional

The purpose of this study is to test the safety of bevacizumab when given in combination with gemcitabine and oxaliplatin and to see what effects (good or bad) it has on patients with hepatocellular carcinoma.

NCT ID: NCT00142428 Completed - Clinical trials for Hepatocellular Carcinoma

Cetuximab in Patients With Unresectable or Metastatic Hepatocellular Carcinoma

Start date: January 2005
Phase: Phase 2
Study type: Interventional

The main purpose of this study is to begin to collect information and to try to learn whether or not cetuximab works in treating patients with unresectable or metastatic hepatocellular carcinoma.

NCT ID: NCT00096733 Completed - Clinical trials for Hepatocellular Carcinoma

Adult-to-Adult Living Donor Liver Transplantation Study

A2ALL-1
Start date: October 2004
Phase: N/A
Study type: Observational

There are two principal purposes of this study: 1) to determine whether it is more beneficial for a liver transplant recipient candidate to pursue a living donor liver transplant (LDLT) or wait for a deceased donor liver transplant (DDLT), and 2) to study the impact of liver donation on the donor's health and quality of life.