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Asian Journal of Urology, 2019, 6(2): 146-152    doi: 10.1016/j.ajur.2018.12.003
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Contemporary approach to active surveillance for favorable risk prostate cancer
Laurence Klotz()
Division of Urology, Sunnybrook Health Sciences Centre, University of Toronto, Toronto, Canada
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Abstract: 

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.

Key words:  Prostate cancer    Active surveillance    Watchful waiting    Conservative management    Low risk
收稿日期:  2018-10-16           接受日期:  2018-10-26      出版日期:  2018-12-15      发布日期:  2019-05-21      整期出版日期:  2019-02-20
引用本文:    
. [J]. Asian Journal of Urology, 2019, 6(2): 146-152.
Laurence Klotz. Contemporary approach to active surveillance for favorable risk prostate cancer. Asian Journal of Urology, 2019, 6(2): 146-152.
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http://www.ajurology.com/CN/10.1016/j.ajur.2018.12.003  或          http://www.ajurology.com/CN/Y2019/V6/I2/146
Pathway Gleason score 3 Gleason score 4
EGF, EGFR [9] No Overexpressed
AKT, MAP2 kinase [8] Expressed Aberrant
HER2neu [9] Expressed Amplified
Insensitivity to growth inhibitory signals (cyclin D2, etc.) [10], [11], [12] Expressed Absent
Resisting apoptosis, BCL2 [13] Negative Strong expression
Absence of senescence, TMPRSS2-ERG [16], [17], [18] ERG normal Increased
VEGF, microvessel density, other pro-angiogenic factors [19], [20] Low expression Increased
PTEN [21] Present in 90% Deleted in 70%-90%
Markers of tissue invasion and metastasis [14], [15] Normal Overexpressed
Clinical evidence of metastasis/PCa mortality [23], [24] Virtually absent Present
  
Low-risk PCa Intermediate risk Tests Other tests 5-ARI
Cancer Care Ontario CUAJ 2015 [56] AS preferred management Active treatment; AS for selected patients PSA 3-6 months DRE 1 yr selected pts MRI when clinical and path findings discordant May have a role
ASCO JCO 2016 [57] Same [1] Same Same Other tests remain investigational No clear role
NICE 2016 [58] Same Radical treatment for “disease progression” [2] PSA 3-4 months, monitor kinetics MRI at enrollment
AUA 2017 [59] Same AS for selected patients Same Same
  
Study n Median follow-up (year) Freedom from treatment bNED after deferred treatment PCa mortality % OS
UCSF [41] 321 3.6 67% at 5 yr 1 recurrence at 3 yr 0 0
University of Toronto [38] 993 8.5 70% at 5 yr 5-yr bNED: 47% 5% at 15 yr 10-yr OS: 68%
Multicentre PRIAS [41] 2494 1.6 77% at 2 yr No data 0 4-yr OS: 87%
University of Miami [42] 230 2.6 85.7% at 5 yr No recurrences 0 No data
Johns Hopkins [43] 1298 5 59% at 5 yr 90.6% recurrence free at 2 yr 0.1% at 15 yr 15-yr OS: 69%
Royal Marsden [44] 471 5.7 70% at 5 yr 85% PSA-failure free at 5 yr 2% at 8 yr 9% at 8 yr
  
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