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GIST clinical trials

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NCT ID: NCT01323400 Completed - GIST Clinical Trials

Efficacy of Pazopanib in Gastrointestinal Stromal Tumors (GIST)

PAZOGIST
Start date: March 2011
Phase: Phase 2
Study type: Interventional

The purpose of this study is to evaluate the antitumor activity of pazopanib in patients with metastatic and/or locally advanced unresectable Gastrointestinal Stromal Tumors (GIST) resistant to imatinib and sunitinib. This is a phase II, randomized, multicentre study.

NCT ID: NCT01246843 Completed - GIST Clinical Trials

Evaluation of Cognitive Function of Patients With Sunitinib or Sorafenib

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

Patients with advanced kidney cancer or GIST (Gastro Intestinal Stromal Tumor: this is a tumor of the intestines) may be eligible for treatment with one of the following drugs: sunitinib (Sutent ®) or sorafenib (Nexavar ®). These drugs inhibit blood vessel formation in cancer cells. These cancer cells are hampered in their growth. To enlarge the investigators knowledge on the effects and side effects of these two medicines, in the University Medical Center St. Radboud lot of research is done. This study is a part of that. Patients receiving sunitinib or sorafenib tell sometimes that they feel that they are less able to concentrate, that their memory is not working properly or that they are less able to imagine a solution to a complex problem . Perhaps you recognize these symptoms as well. In how many of the patients this occurs, how severe the symptoms are and how it is caused, is still unknown. The goal of this research is to examine how memory, concentration and knowledge processing works in patients using sorafenib or sunitinib. With the research the investigators hope to get answers to the following questions: 1. How common are problems with memory, concentration and processing of knowledge in patients receiving the drug sunitinib or sorafenib? 2. What are the problems of memory, concentration and processing of knowledge in the use of sunitinib or sorafenib? 3. What could be the cause of the problems that patients experience from memory, concentration and processing of knowledge in the use of sunitinib or sorafenib? 4. Is there a link between problems with memory, concentration and processing of knowledge and also experiences of fatigue or mood of a patient?

NCT ID: NCT00979381 Completed - Clinical trials for Renal Cell Carcinoma

Study of the Immunoresponse in Patients Treated With a Tyrosine Kinase Inhibitor

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

In this study the researchers investigate the influence of the tyrosine kinase inhibitors sunitinib and sorafenib, on the normal humoral and cellular immuno response to influenza vaccination in patients with metastases of renal cell carcinoma or a GIST.

NCT ID: NCT00979329 Completed - Colorectal Cancer Clinical Trials

Study on the Influence of Sunitinib and Sorafenib on Fatigue, QoL, Depression in Patients With Metastatic RCC or GIST

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

The purpose of this study is to assess the influence of Sunitinib and Sorafenib on fatigue, quality of life and depression in patients with metastatic renal cell or colorectal cancer or GIST. In order to get more insight in the mechanism of vascular endothelial growth factor (VEGF) related fatigue and if possible to come to a resolution for this side effect.

NCT ID: NCT00618319 Completed - GIST Clinical Trials

An Open-Label, 18FDG-PET Pharmacodynamic Assessment of the Effect of BIIB021 in Subjects With Gastrointestinal Stromal Tumors (GIST)

Start date: February 2008
Phase: Phase 2
Study type: Interventional

This study will examine the effect of BIIB021 on GIST growth and metabolism.

NCT ID: NCT00399152 Completed - Renal Cancer Clinical Trials

Perifosine + Sunitinib Malate for Patients With Advanced Cancers

Start date: October 2006
Phase: Phase 1
Study type: Interventional

This study is a Phase I trial in two parts. In part 1, a MTD to the combination of perifosine and sunitinib malate will be determined. In part 2, with the MTD as a starting point, a group of patients will be accrued with the goal of ensuring that they will be able to tolerate at least two courses of therapy, which would make them evaluable for response in a Phase II study.