Evaluation of Cognitive Function of Patients With Sunitinib or Sorafenib
NCT ID: NCT01246843
Last Updated: 2011-11-02
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
50 participants
OBSERVATIONAL
2009-07-31
2011-04-30
Brief Summary
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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?
Detailed Description
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Conditions
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Study Design
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CASE_ONLY
PROSPECTIVE
Study Groups
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metastatic Renal Cell Carcinoma without treatment
patients with metastasized RCC who did not receive treatment
No interventions assigned to this group
mRCC with treatment
patients with metastastic renal cell cancer or GIST who are on treatment with Sunitinib or Sorafenib for
≥ 8 weeks
No interventions assigned to this group
Eligibility Criteria
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Inclusion Criteria
* patients with metastatic renal cell cancer or GIST who are on treatment with Sunitinib or Sorafenib for ≥ 8 weeks
* Karnofsky score \> 70%
* age \> 18 year.
* written informed consent for study
Patient controls selection
* patients with metastatic renal cell cancer or GIST who aren't treated yet (only interferon alfa or interleukine 2 treatment is allowed when \> 12 months ago.
* Karnofsky score \> 70%
* age \> 18 year.
* written informed consent for study
Exclusion Criteria
* contra-indications for treatment with Sunitinib or Sorafenib
* patients who do not speak or write the Dutch language adequately
* known brain metastasis
* use of psychiatric or anti-epileptic medication
* known cognitive disorders unrelated to diagnosis or medication use
* radiotherapy on the brain at any time in the past
* systemic chemotherapy
* in the last 12 months interferon alfa or interleukin-2 treatment
* operation in the last 3 months
* Stroke/TIA (transient ischaemic attack)
Patient controls section:
* patients who do not speak or write the Dutch language adequately
* known brain metastasis
* use of psychiatric or anti-epileptic medication
* known cognitive disorders unrelated to diagnosis or medication use
* radiotherapy on the brain at any time in the past
* systemic chemotherapy
* in the last 12 months interferon alfa or interleukin-2 treatment
* operation in the last 3 months
* stroke/TIA (transient ischaemic attack)
18 Years
ALL
No
Sponsors
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Radboud University Medical Center
OTHER
Responsible Party
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Principal Investigators
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C.M.L. van Herpen, Md PhD
Role: PRINCIPAL_INVESTIGATOR
University Medical Centre Nijmegen
Locations
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University Medical Centre Nijmegen
Nijmegen, Gelderland, Netherlands
Countries
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References
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Mulder SF, Bertens D, Desar IM, Vissers KC, Mulders PF, Punt CJ, van Spronsen DJ, Langenhuijsen JF, Kessels RP, van Herpen CM. Impairment of cognitive functioning during Sunitinib or Sorafenib treatment in cancer patients: a cross sectional study. BMC Cancer. 2014 Mar 24;14:219. doi: 10.1186/1471-2407-14-219.
Other Identifiers
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UMCNONCO200904
Identifier Type: -
Identifier Source: org_study_id