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. Author manuscript; available in PMC: 2016 Oct 1.
Published in final edited form as: Nat Rev Urol. 2016 Mar 8;13(4):205–215. doi: 10.1038/nrurol.2016.45

Table 2.

Monitoring protocols and triggers for intervention.

Intervals of surveillance Triggers for intervention*
PSA (mo.) Exam (mo.) Mandatory confirmatory biopsy (≤ 1 yr.) Subsequent biopsies (yrs. from previous) Gleason score Positive cores Max % core with cancer PSAV PSADT (yr)
Johns Hopkins# 6 6 Yes 1 >6 >2 >50
Sunnybrook 3 (x2 yr) then 6 Yes 3–4 Upgrade < 3
Göteborg 3–6 3–6 No 2–3 Progression in PSA, grade, or stage (not strictly defined)
UCSF 3 6 Yes 1–2 >6 >33% >50
Royal Marsden 3–4 (x2 yr) then 6 3–4 (x2 yr) then 6 No (≤ 2 yrs.) 2 ≥4+3 >50% >1
St. Vincent’s 3 (x3 yr) then 6 6 (x3 yr) then 12 Yes 1–2, then 3–5 >6 >20% >8 mm >0.75 < 3
PRIAS 3–6 Yes 3 >6 >2 < 3
University of Copenhagen 3 3 Yes Variable ≥4+3 >3 < 3
University of Miami 3–4 (x2 yr) then 6 3–4 (x2 yr) then 6 Yes 1 >6 >2 Increase
*

The majority of programs describe criteria that trigger increased scrutiny (i.e. repeat biopsy, imaging) but not necessarily treatment. These metrics include: clinical stage, CAPRA score, PSA/PSA kinetics (if not a formal trigger for intervention).

#

For low risk men, number of cores positive and maximum percentage of cancer involvement are not triggers for intervention.

Until 2008