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dc.contributor.author Sotomayor, Paula C.
dc.contributor.author Aguilar, Juan C.
dc.contributor.author Mujica, Karen
dc.contributor.author Zuñiga, Alvaro
dc.contributor.author Godoy, Alejandro S.
dc.contributor.author Smith, Gary J.
dc.contributor.author Mohler, James L.
dc.contributor.author Vitagliano, Gonzalo
dc.contributor.author San Francisco, Ignacio F.
dc.date.accessioned 2024-09-26T00:26:46Z
dc.date.available 2024-09-26T00:26:46Z
dc.date.issued 2022-12-01
dc.identifier.issn 0042-1138
dc.identifier.uri https://repositorio.uss.cl/handle/uss/12172
dc.description Publisher Copyright: © 2022 IGI Global. All rights reserved.
dc.description.abstract Background: Prostate cancer (PCa) represents one of the most frequent malignancies and the fifth leading cause of cancer death in adult men worldwide. PCa mortality rates have been declining in several Western countries; one of the possible reasons may be related to the application of prostate-specific antigen early detection policies. These early detection protocols increase PCa-specific patient survival; however, a high percentage of these cases corresponds to low-risk PCa that grows very slowly and is unlikely to metastasize to threaten survival. Many low-risk PCa patients receive aggressive therapies, such as radical prostatectomy and radiotherapy, that are costly for patients and/or health systems and generate side effects that affect the quality of life. An alternative to surgery and radiotherapy treatments for low-risk PCa is active surveillance (AS), a strategy based on close disease monitoring and intervention only if the disease progresses. However, proper identification of low-risk PCa patients at the time of diagnosis is essential for the effectiveness AS. The selection of AS candidates remains challenging; thus, effective prognostic biomarkers are needed. Summary: This review article addresses the characteristics of the current and emerging PCa prognostic biomarkers, including tests available for tissue, blood, and urine analyses, for the appropriate selection of PCa patients for AS. In addition, and based on published literature, we performed a selection of potential new biomarkers that can distinguish low-risk PCa. Key Messages: The literature search yielded four tissue-based tests, two blood-based tests, and six urine-based tests that can be used to determine PCa risk classification. However, most available tests are expensive; thus, cost-effective analyses are needed in order to obtain the approval of government agencies and to be financed by the health systems. Available prognostic urine tests have shown great progress over the last years, and they have the advantage of being minimally invasive; therefore, they may become a routine disease progression test for patients under AS. In addition, new research conducted in the last decade has shown promising biomarkers, including mRNA, miRNA, long noncoding RNA, and metabolites, that could improve existing tests or allow the development of new tools for AS patient selection. en
dc.language.iso eng
dc.relation.ispartof vol. 106 Issue: no. 12 Pages: 1201-1213
dc.source Urologia Internationalis
dc.title Active Surveillance in Prostate Cancer : Current and Potentially Emerging Biomarkers for Patient Selection Criteria en
dc.type Artículo de revisión
dc.identifier.doi 10.1159/000527151
dc.publisher.department Facultad de Medicina y Ciencia


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