Page 4 - Canadian Urological Association recommendations on prostate cancer screening and early diagnosis
P. 4

Guideline: PSA screening and early diagnosis




       however, a recently published case-control study nested   study including men undergoing annual PSA screening iden-
       within the Physicians Health Study cohort identified that   tified that men with a PSA <1 ng/ml had a 10-year prostate
       the risk of developing metastatic prostate cancer within 15   cancer detection rate of only 3.4%, of which 90% were con-
                                                                           40
       years among men in this age group was very low, even   sidered low-risk.  Furthermore, the nested case-control study
                                               38
       among men with PSA levels in the top decile.  Thus, PSA   referenced above identified that the risk of developing meta-
       testing in these men may lead to biopsies and diagnoses   static disease within 15 years for a man of any age with PSA
                                                                                39
       that are unlikely to provide benefit. The potential delay in   <1 ng/ml is very low.  As such, allowing a longer interval
       diagnosis in the small proportion of men at this age with   between PSA testing for these men is unlikely to result in an
       clinically significant prostate cancer seems unlikely to lead   increase in prostate cancer morbidity or mortality and will
       to a missed opportunity for curative treatment.       potentially reduce the risk of over-detection as a result of lead-
         These recommendations are not directed towards men   time bias or natural fluctuations in PSA levels.
       with known germ-line mutations associated with prostate    On the other hand, as baseline PSA levels rise above 1
       cancer development (e.g., BRCA1, BRCA2, HOXB13). In   ng/ml, the intermediate-term risk of developing both any
       these cases, an individualized testing strategy after consulta-  prostate cancer and clinically significant prostate cancer
       tion with a clinical geneticist is most appropriate.  increases substantially. 39-41  As such, we recommend that
         3.	 For men electing to undergo PSA screening, we sug-  these men, if electing PSA screening, should undergo test-
             gest that the intervals between testing should be  ing every two years. The ERSPC trial considered a positive
             individualized based on previous PSA levels (Fig. 1).  test to be a PSA level of 3 ng/ml, while the Goteborg trial
             a.	 For men with PSA <1 ng/ml, repeat PSA test-  considered a positive test to be between 2.5 and 3.4 ng/ml
                 ing every four years (Level of evidence: 3;   (depending on the year of study). Thus, the optimal frequen-
                 Grade of recommendation: C).                cy of PSA testing in men above these levels is unknown. For
             b.	 For men with PSA 1–3 ng/ml, repeat PSA test-  men with PSA >3 ng/ml, more frequent PSA testing intervals
                 ing every two years (Level of evidence: 3;   can be considered. In addition, adjunctive testing strategies
                 Grade of recommendation: C).                that estimate the risk of clinically significant disease may be
             c.	 For men with PSA >3 ng/ml, consider more    helpful for biopsy decision-making in these men (see below).
                 frequent PSA testing intervals or adjunctive   4.	 For men electing to undergo PSA screening, we sug-
                 testing strategies (Level of evidence: 4; Grade   gest that the age at which to discontinue PSA screen-
                 of recommendation: C).                            ing should be based on current PSA level and life
       Justification: Although the frequency at which PSA screen-  expectancy.
       ing should be performed has not been rigorously studied     a.	 For men aged 60 with a PSA <1 ng/ml, con-
       to date, we can extrapolate from the existing clinical trials   sider discontinuing PSA screening (Level of
       and observational studies to provide some guidance on this      evidence: 2; Grade of recommendation: C).
       issue. In particular, men in the screening arms of the ERSPC   b.	 For all other men, discontinue PSA screening
       trial and Goteborg trial underwent testing at intervals of      at age 70 (Level of evidence: 2; Grade of rec-
       four and two years, respectively, providing the basis for our   ommendation: C).
       recommendations.                                            c.	 For men with a life expectancy less than 10
         For men with a PSA level <1ng/ml, longer intervals between    years, discontinue PSA screening (Level of evi-
       PSA testing are appropriate. Indeed, a large prospective cohort   dence: 4; Grade of recommendation: C).



                                                   Repeat testing
                                                   every 4 years a,b
                                     PSA<1

            Prostate cancer
            screening shared         PSA 1–3       Repeat testing
            decision-making                        every 2 years a
             (ages 50–70)

                            PSA>3
                                       More frequent            Consider adjunctive            Biopsy shared
                                        PSA testing c              strategies d                decision-making
                                                     PSA elevated                   Abnormal
       Fig. 1. Prostate cancer screening pathway.  Discontinue screening if life expectancy <10 years;  consider discontinuation of screening if age >60 and PSA <1 ng/ml;
                                   a
                                                                    b
       c more frequent testing interval can be considered; the optimal frequency is unknown;  i.e., risk calculators, % free PSA, etc. PSA: prostate-specific antigen.
                                                              d
                                                 CUAJ • October 2017 • Volume 11, Issue 10                    301
   1   2   3   4   5   6   7   8   9