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Liver Neoplasms clinical trials

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NCT ID: NCT02156739 Active, not recruiting - Clinical trials for Hepatocellular Carcinoma

Contrast-enhanced MRI in Detecting Benign and Malignant Liver Lesions

Start date: October 13, 2014
Phase: N/A
Study type: Interventional

This clinical trial studies contrast-enhanced magnetic resonance imaging (MRI) in detecting nonmalignant and malignant liver lesions. Diagnostic procedures, such as MRI, may help find and diagnose nonmalignant and malignant liver lesions. Contrast agents, such as gadoxetate disodium and gadobutrol, may help doctors to see MRI images more clearly.

NCT ID: NCT02145559 Completed - Lymphoma Clinical Trials

A Pharmacodynamic Study of Sirolimus and Metformin in Patients With Advanced Solid Tumors

Start date: April 2014
Phase: Phase 1
Study type: Interventional

Given the role of mTOR signaling and probable synergistic activity of combining sirolimus and metformin in patients with advanced solid tumors, the investigators hypothesize that: 1. The combination of metformin plus sirolimus will result in reduction of p4EBP1, p70S6K and pAKT more than sirolimus alone in peripheral blood T cells (PBTC). 2. The combination of metformin plus sirolimus will result in decreased levels of serum biomarkers including fasting insulin, C-peptide, glucose, triglycerides, LDH, IGF-1, IGF-1R, IGF-BP and leptin, but an increase in adiponectin in peripheral blood. 3. Expression of active forms of AMPK, mTOR, PI3K, PTEN loss, AKT, LKB1, P62, LC3, and/or ULK1 in the tumor tissue (original pathology) will be predictive of response to combination therapy. This will be an exploratory hypothesis for this study. 4. Sirolimus induced toxicity, especially hyperglycemia and hypertriglyceridemia, will be mitigated by combining sirolimus with metformin. 5. Metformin plus sirolimus will have promising anti-cancer activity and this activity will correlate with decreases in the above biomarkers. This will be an exploratory hypothesis for this study.

NCT ID: NCT02145013 Active, not recruiting - Clinical trials for Primary Liver Cancers

Portal Hypertension and Liver Resection in Patients With Hepatocellular Carcinoma

Start date: November 2013
Phase: N/A
Study type: Observational

According to the BCLC guidelines, surgical resection of hepatocellular carcinoma complicating cirrhosis is restricted to patients with preserved liver function, single nodule without vascular invasion and with hepatic venous gradient below 10 mmHg. However, other guideline treatment, especially from eastern countries demonstrated that surgical resection is safe and feasible and provides better survival than the treatment recommended by the BCLC system for patients with similar stage. The primary goal of this study is to assess the impact of HVPG on short and long-term outcomes in HCC patients who undergo liver resection.

NCT ID: NCT02141906 Completed - Clinical trials for Hepatocellular Cancer

A Pilot Study of "OncozeneTM" Microspheres for Intra-arterial Delivery of Doxorubicin

Start date: January 21, 2015
Phase: Phase 2
Study type: Interventional

This is a pilot study of Onconzene Microspheres for intra-arterial delivery of doxorubicin for the treatement of patients with unresectable hepatocellular cancer.

NCT ID: NCT02119065 Active, not recruiting - Liver Metastases Clinical Trials

Pilot Study to Assess Lung Shunting of Yttrium-90 Microspheres Using PET/CT

Start date: January 30, 2014
Phase:
Study type: Observational

This pilot clinical trial studies positron emission tomography (PET)/computed tomography (CT) in finding beads after Yttrium-90 bead therapy in patients with primary liver cancer or cancer that has spread to the liver (metastatic) that can not be removed by surgery. Imaging procedures, such as PET/CT after Yttrium-90 bead therapy, may help see if the beads are present in the lung and compare the results with the pre-therapy imaging.

NCT ID: NCT02095236 Withdrawn - Tumor Clinical Trials

Evaluation of Intrafractional Motion of Liver Tumors Using Markers

ESMERALDA
Start date: n/a
Phase: N/A
Study type: Interventional

Radioopaque fiducial markers or electro-magnetic transponders will be implanted into or in close proximity of the tumor. During a radiotherapy treatment session image and/or signal acquisition will be performed by ultrasound, computed tomography, magnetic resonance imaging or by specialized signal detectors The data will help to characterize tumor and organ motion during one treatment session which may in fact have impact on dose distribution

NCT ID: NCT02094625 Completed - Osteosarcoma Clinical Trials

NAC to Prevent Cisplatin-induced Hearing Loss

Start date: March 2016
Phase: Phase 1
Study type: Interventional

Cisplatin is a key chemotherapy agent for the treatment of multiple childhood cancers but causes permanent hearing loss. This study investigates the drug N-acetylcysteine (NAC) to determine the dose necessary to protect hearing and also how well tolerated NAC is when combined with chemotherapy.

NCT ID: NCT02089919 Completed - Neoplasms, Liver Clinical Trials

Cancer Stem Cells Vaccine Therapy in Treating Hepatocellular Cancer Patients

Start date: February 2014
Phase: Phase 1/Phase 2
Study type: Interventional

Most studies of cancer stem cells (CSC) involve the inoculation of cells from human tumors into immunosuppressed mice, preventing an assessment on the immunologic interactions and effects of CSCs. In this study, the investigators examined the vaccination effects produced by CSC-enriched populations from histologically distinct murine tumors after their inoculation into different syngeneic immunocompetent hosts. Enriched CSCs were immunogenic and more effective as an antigen source than unselected tumor cells in inducing protective antitumor immunity.Immune sera from CSC-vaccinated hosts contained high levels of IgG which bound to CSCs, resulting in CSC lysis in the presence of complement.CTLs generated from peripheral blood mononuclear cells or splenocytes harvested from CSC-vaccinated hosts were capable of killing CSCs in vitro. Mechanistic investigations established that CSC-primed antibodies and T cells were capable of selective targeting CSCs and conferring anti-tumor immunity.

NCT ID: NCT02088775 Completed - Clinical trials for Unspecified Adult Solid Tumor, Protocol Specific

PET-CT in Determining the Radioembolization Dose Delivered to Patients With Liver Metastasis, Primary Liver Cancer, or Biliary Cancer

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

This clinical trial studies positron emission tomography (PET)-computed tomography (CT) in determining the radiation dose delivered with radioactive spheres to patients with liver metastasis or primary liver or biliary cancer. Comparing results of diagnostic procedures dose before and after delivery of radioactive spheres to the liver may help determine radioembolization dose and plan the best treatment for liver metastasis or primary liver or biliary cancer.

NCT ID: NCT02086656 Completed - Clinical trials for Colorectal Cancer Liver Metastases

PERIOPERATIVE TREATMENT WITH COI-B (CAPECITABINE, OXALIPLATIN, IRINOTECAN AND BEVACIZUMAB) OF HIGH RISK OR BORDERLINE RESECTABLE COLORECTAL CANCER LIVER METASTASES

COI-B
Start date: June 2013
Phase: Phase 2
Study type: Interventional

Capecitabine, oxaliplatin, irinotecan and bevacizumab as perioperative strategy of borderline and/or high risk resectable colorectal cancer liver metastases