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Contemporary approach to active surveillance for favorable risk prostate cancer

The approach to favorable risk prostate cancer known as “active surveillance” was first described explicitly in 2002. This was a report of 250 patients managed with a strategy of expectant management, with serial prostate-specific antigen and periodic biopsy, and radical intervention advised for pat...

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Autor principal: Klotz, Laurence
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Second Military Medical University 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488691/
https://www.ncbi.nlm.nih.gov/pubmed/31061800
http://dx.doi.org/10.1016/j.ajur.2018.12.003
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author Klotz, Laurence
author_facet Klotz, Laurence
author_sort Klotz, Laurence
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description The approach to favorable risk prostate cancer known as “active surveillance” was first described explicitly in 2002. This was a report of 250 patients managed with a strategy of expectant management, with serial prostate-specific antigen and periodic biopsy, and radical intervention advised for patients who were re-classified as higher risk. This was initiated as a prospective clinical trial, complete with informed consent, beginning in 2007. Thus, there are now 20 years of experience with this approach, which has become widely adopted around the world. In this chapter, we will summarize the biological basis for active surveillance, review the experience to date of the Toronto and Hopkins groups which have reported 15-year outcomes, describe the current approach to active surveillance in patients with Gleason score 3 + 3 or selected patients with Gleason score 3 + 4 with a low percentage of Gleason pattern 4 who may also be candidates, enhanced by the use of magnetic resonance imaging, and forecast future directions.
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spelling pubmed-64886912019-05-06 Contemporary approach to active surveillance for favorable risk prostate cancer Klotz, Laurence Asian J Urol Review The approach to favorable risk prostate cancer known as “active surveillance” was first described explicitly in 2002. This was a report of 250 patients managed with a strategy of expectant management, with serial prostate-specific antigen and periodic biopsy, and radical intervention advised for patients who were re-classified as higher risk. This was initiated as a prospective clinical trial, complete with informed consent, beginning in 2007. Thus, there are now 20 years of experience with this approach, which has become widely adopted around the world. In this chapter, we will summarize the biological basis for active surveillance, review the experience to date of the Toronto and Hopkins groups which have reported 15-year outcomes, describe the current approach to active surveillance in patients with Gleason score 3 + 3 or selected patients with Gleason score 3 + 4 with a low percentage of Gleason pattern 4 who may also be candidates, enhanced by the use of magnetic resonance imaging, and forecast future directions. Second Military Medical University 2019-04 2018-12-15 /pmc/articles/PMC6488691/ /pubmed/31061800 http://dx.doi.org/10.1016/j.ajur.2018.12.003 Text en © 2019 Editorial Office of Asian Journal of Urology. Production and hosting by Elsevier B.V. http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Review
Klotz, Laurence
Contemporary approach to active surveillance for favorable risk prostate cancer
title Contemporary approach to active surveillance for favorable risk prostate cancer
title_full Contemporary approach to active surveillance for favorable risk prostate cancer
title_fullStr Contemporary approach to active surveillance for favorable risk prostate cancer
title_full_unstemmed Contemporary approach to active surveillance for favorable risk prostate cancer
title_short Contemporary approach to active surveillance for favorable risk prostate cancer
title_sort contemporary approach to active surveillance for favorable risk prostate cancer
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6488691/
https://www.ncbi.nlm.nih.gov/pubmed/31061800
http://dx.doi.org/10.1016/j.ajur.2018.12.003
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