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Article

Active Surveillance for Prostate Cancer: Patient Selection and Management

University of Toronto and Sunnybrook Health Sciences Centre, Toronto, ON M4N 3M5, Canada
Curr. Oncol. 2010, 17(s2), 11-17; https://doi.org/10.3747/co.v17i0.713
Submission received: 4 June 2010 / Revised: 3 July 2010 / Accepted: 6 August 2010 / Published: 1 September 2010

Abstract

Screening for prostate cancer using prostate-specific antigen (PSA) has been appealing. However, the significant associated decline in prostate cancer mortality comes at the cost of a very high rate of diagnosis, and many patients with indolent, non-life-threatening cancer are exposed to the risk of significant side effects from radical treatment. Most men with favourable-risk prostate cancer are not destined to die of their disease, even in the absence of treatment. The challenge is to identify the subset that harbour more aggressive disease early enough that curative therapy is still a possibility, thereby allowing the others to enjoy improved quality of life, free from the side effects of treatment. This article reviews current research into active surveillance in favourable-risk disease and some of the issues that arise when prostate cancer is monitored rather than being treated immediately.
Keywords: cancer screening; psa; overdiagnosis; active surveillance cancer screening; psa; overdiagnosis; active surveillance

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MDPI and ACS Style

Klotz, L. Active Surveillance for Prostate Cancer: Patient Selection and Management. Curr. Oncol. 2010, 17, 11-17. https://doi.org/10.3747/co.v17i0.713

AMA Style

Klotz L. Active Surveillance for Prostate Cancer: Patient Selection and Management. Current Oncology. 2010; 17(s2):11-17. https://doi.org/10.3747/co.v17i0.713

Chicago/Turabian Style

Klotz, L. 2010. "Active Surveillance for Prostate Cancer: Patient Selection and Management" Current Oncology 17, no. s2: 11-17. https://doi.org/10.3747/co.v17i0.713

APA Style

Klotz, L. (2010). Active Surveillance for Prostate Cancer: Patient Selection and Management. Current Oncology, 17(s2), 11-17. https://doi.org/10.3747/co.v17i0.713

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