low risk prostate carcinoma Maurizio Brausi

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1 Watchful Waiting and Active surveillance for low risk prostate carcinoma Maurizio Brausi

2 Un programma di sorveglianza attiva e alla portata di tutti i centri?

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5 EAU guidelines 2012: Indications

6 Active Surveillance: Follow-up Patients who are in AS protocols should be controlled periodically. * PSA every 6 months * Prostate Biopsy at 1-2 years * MRI could be used instead prostate biopsy?

7 A Multisciplinary Approach To Prostate Cancer

8 WHY A MULTIDISCIPLINARY MANAGEMENT OF CANCER?

9 AIMS OF A MULTIDISCIPLINARY TEAM FOR CANCER (Prostate t Cancer Unit)

10 PROSTATE CANCER UNIT Ausl Modena

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12 D: Un Programma di AS è alla portata t di tutti tti i Centri Ospedalieri? Risposta: E alla portata della maggior parte dei centri Ospedalieri che hanno la possibilità di controllare i pazienti periodicamente e di eseguire biopsie prostatiche in tempi adeguati. L approccio multidisciplinare dovrebbe essere una priorità ità

13 In cosa un programma di AS differisce da un programma di WW?

14 EAU guidelines 2012: definizioni

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16 EAU guidelines 2012: WW in PC T1-2/N0/M0

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22 EAU guidelines 2014: AS

23 EAU Guidelines 2014: AS

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28 D: In cosa Differisce i un programma di AS da un programma di WW? Risposta Un programma di AS prevede l attento e periodico monitoraggio del paziente (ogni 6 mesi con PSA) e controllo della prostata con biopsia ogni 1-2 anni. Un programma di WW non prevede controlli periodici e tratta il paziente alla presenza di eventuali sintomi.

29 Risks of Active Surveillance Protocols

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31 Active Surveillance It is not a strategy for everyone with low risk PC but should ldbe one option or probably bl the first option. It is not a passive approach The primary goal is not to decrease overtreatment but to maximize the quality yof life eon an individual du basis s

32 Active Surveillance One should not treat PC as early as possible but as late as possible while still curable with low morbidity Overtreatment is not only associated to negative impact on Quality of Life but is also very costly

33 Side-effects from treatment Permanent side-effects from treatment are common and results in lowered quality of life!! Side-effects effects are significantly lower if treated by the most skilful surgeons in high volume centers, but how is it on an average?

34 Patient Selection For AS Variable, according to different International protocols: 1-2 core of Pca Gleason score < 15% in the core at standard biopsy Different Methods of diagnosis: If we use standard (12 cores Biopsy) we miss about 30-35% of significant cancer (Gleason score 7). This was studied by a group who performed Template biopsy in patients on AS selected with standard biopsy

35 Selecting Patients For AS Multiparametric MRI (3 Tesla) with targeted biopsy will be the future (US Fusion) The standard in 2013 for diagnosis and patient selection AS is Template biopsy

36 5 deaths in PC but only one y was low risk

37 60 % of all screen-detected cancers were of low risk

38 Failure rate measured as tumor recurrence after active treatment (PSA relapse or hormonal treatment)

39 What is the problem with AS Close and life long FU contribute to stigmatise the patient Knowing having PC may cause psychological trauma which in certain individuals may burden the quality of life more than side effects from treatment We have no validated trigger points for switching to active treatment Treating men after progression may cause more sideeffects than treating men early

40 Conclusions Low risk PC is low risk, but be careful some are falsely staged, early re-evaluation!! evaluation!! The overwhelming majority of men with low risk PC will never develop symptoms and will die from other causes AS with delayed active treatment in those who need seem to be as effective as treating all actively from start Existing active treatments that are evidence based are associated with side-effects that will considerably affect quality of life in many patients Surveillance will maximise quality of life and reduce costs

41 Future Goals Find strategies to avoid diagnosing insignificant low risk PC Better screening tools for detecting biologically significant cancers Biopsy men more selectively and change from systematic to imaging gguided biopsies

42 What is the risk with low risk PC? Rider et al Eur Urol 2012 Popiolek et al Eur Urol 2012 Klotz et al JCO 2010 Godtman et al Eur Urol 2012 T d t t ti t h ill d To undertreat patients who will progress and develop metastatic disease

43 Pro Surveillance Jonas Hugosson Dept of Urology, Sahlgrenska Academy, Göteborgs Universitet Sweden