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This non-interventional study includes patients with advanced and/or metastatic renal cell carcinoma who are treated with SUTENT and who did not receive any other systemic therapy before. The aim of the trial is to increase knowledge about quality of life, safety, efficacy and tolerability under conditions of routine use of Sutent. The individual observation period of each patient will be
1 year.
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The Statistical Analysis Plan provides detailed specification of the analysis
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356 participants in 1 patient group
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Data sourced from clinicaltrials.gov
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