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Urol Oncol ; 29(4): 447-53, 2011.
Article in English | MEDLINE | ID: mdl-21726795

ABSTRACT

Clinical trials often report surrogate endpoint data. A surrogate endpoint is a biological marker or clinical sign that can be substituted for a patient-important outcome. Using surrogate endpoints correctly may facilitate and expedite clinical trials and may improve medical decisions. However, rigorous criteria must be met for an endpoint to be considered a valid surrogate. The purpose of this article is to review the topic of surrogate endpoints in the context of a urologic encounter.


Subject(s)
Biomarkers/analysis , Evidence-Based Medicine , Urologic Neoplasms/diagnosis , Androgen Antagonists/therapeutic use , Humans , Male , Neoplasm Metastasis , Prognosis , Prostate-Specific Antigen/analysis , Prostatic Neoplasms/diagnosis , Prostatic Neoplasms/drug therapy , Prostatic Neoplasms/metabolism , Urologic Neoplasms/drug therapy , Urologic Neoplasms/metabolism
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