GIST, Renal Cell Carcinoma
Conditions
Keywords
sunitinib, sorafenib, immune response
Brief summary
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.
Detailed description
When cure is not longer possible, cancer patients enter the palliative phase. For many types of cancer several treatment options are available. The goal of this treatment is to prolong survival, but maintenance or even improvement of quality of life is of equal importance. The currently available systemic treatment options consist of conventional cytotoxic therapy, hormonal therapy, immunotherapy and the so-called targeted therapies. Combinations of these therapies are also being used. Targeted therapy concerns the application of a new class of drugs that are specifically directed against one or more well-defined molecular targets that are relevant for carcinogenesis, cell cycle regulation, tumour progression, metastasis, tumour angiogenesis and/or apoptosis. Today, the most successful drugs in this class are directed against the vascular endothelial growth factor (VEGF) and the epidermal growth factor receptor (EGFR). There is an explosive development ongoing in this field and many new drugs become available that have new targets or inhibit a combinations of targets. Meanwhile, targeted therapy has shown efficacy in many types of cancer and is registered for several indications. The toxicity profile of targeted therapies is still largely unknown, and the aetiology of many known side effects has not been clarified. At the moment, three targeted therapies that are directed against VEGF are registered and used in the Netherlands: Sunitinib (Sutent®) and Sorafenib (Nexavar ®) both oral drugs and Bevacizumab (Avastin®), an intravenously drug. Clinical experience and some mouse studies show that targeted therapies could have a negative effect on the immune response. This can be of great influence on patients who are treated with this type of drug. Especially because these drug will be used chronically and sometimes for years and infections can have a large influence on the health and quality of life of these patients.
Interventions
BIOLOGICALinfluenza vaccine
influenza vaccination
Sponsors
Radboud University Medical Center
Study design
Observational model
COHORT
Time perspective
PROSPECTIVE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
Yes
Inclusion criteria
* Patients with metastasized renal cell carcinoma or GIST who have been treated with sunitinib or sorafenib for at least 4 weeks, or patients with metastasized RCC who did not receive a systemic treatment for their RCC (nephrectomy is allowed) * Patients who are indicated for influenza vaccination and and have been summoned for this vaccination by their GP * age ≥18 years (for the healthy volunteers: age≥ 60 years) * signed Informed Consent Form
Exclusion criteria
* patients with an identified immunodeficiency disorder * patients that have been treated with corticosteroids in the past 2 weeks or who are still using these (except for a short period \<10 days) * patients that are treated with immunotherapy in the last year (ex. interferon-alpha of IL-2) or who have received another form of targeted therapy (ex. bevacizumab). * patients with symptoms of influenza at the time of vaccination * patient with an allergy for chicken-eggwhite
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| cellular and humoral immune response | 1 year |
Secondary
| Measure | Time frame |
|---|---|
| times the influenza virus occurs | 1 year |
Countries
Netherlands
Outcome results
None listed