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Editorial

Referring to the article published on pp. 899

907 of this issue

Real-time Watchful Surveillance Looks Like Active Waiting

Chris Bangma

* , Monique Roobol

Department of Urology, Erasmus University Medical Centre, Rotterdam, The Netherlands

Once upon a time, many years ago, when active surveillance

(AS) had not yet been invented, and there were hardly any

computers that couldmanage the heavy computational load

for Markov modeling, a cohort of men diagnosed with

prostate cancer initially decided not to be treated; this

sounds like a fairy tale, but it was only 20 yr ago. The

substantial cohort of more than 600 Finnish, Swedish, and

Dutch men participated in the ERSPC prostate cancer

screening trial and were observed until death. No-one

followed a structured monitoring protocol with scheduled

repeat biopsies, and switches to active therapy were not

related to potential signs of progression. The overall 10-yr

survival was 77%, and no man died of prostate cancer

[1]

,

which represents excellent results.

This was not the first group on expected management.

T1a disease (

<

5% of transurethral resection of the prostate

samples positive for prostate cancer) was still frequently

seen because medical treatment for obstructive clinical

benign prostatic hyperplasia was not that common. The

guidelines at that time advised no further diagnostic or

therapeutic interventions in cases with well-differentiated

adenocarcinoma. Outcomes were good, with disease-

specific survival of

>

95% at 15 yr

[2]

.

Men diagnosed with low-risk prostate cancer may

choose monitoring instead of invasive treatment to avoid

unwanted side effects of (immediate) treatment. Alterna-

tively, they may opt for maximal security and control by

following protocols including rebiopsy, imaging, and even

genetic profiling of their tumor. Or they may choose

minimal monitoring by deciding not even to repeat

prostate-specific antigen (PSA) measurements and to wait

for certain symptoms to occur: the traditional watchful

waiting (WW). Most men who are comfortable with the

ease of an annual medical check-up like to follow their PSA

periodically, and certainly when they are older than 75 yr or

when serious comorbidity exists. They invent their own

follow-up protocol with which they are satisfied: active

waiting.

The modeled comparison of different AS protocols and

WW in the article by Loeb et al

[3]

helps in advising men

with low-risk tumors according to the traditional param-

eters of Gleason score, estimated tumor size (in line with

the number of positive cores in systematic biopsies), and

PSA levels. Indeed, we are unable to provide level 1 scientific

evidence from clinical studies, and we will never be able to.

The modeling tries to map uncertainties around the impact

of events such as biopsies and treatment on quality of life

(QOL) as much as possible by using utilities taken from the

literature.

The model illustrates the theoretical remaining (quality-

adjusted) life expectancy after diagnosis of localized

prostate cancer when following either a WW approach or

an AS protocol, assuming 100% compliance with the

different diagnostic tests. But real life is different. Strict

compliance to protocols appears to be difficult for patients

and physicians

[4,5] ,

and protocol adjustment over time to

preferences that minimize diagnostic interventions includ-

ing biopsies and PSA measurements is evident. We do not

know about imaging compliance, and this might be very

dependent on nonmedical factors such as availability and

reimbursement of costs.

Some of the authors

conclusions follow our intuition

and are self-evident. Following a strict protocol (including

invasive treatment when tumor reclassification towards

higher risk occurs) provides better clinical outcomes than

waiting for symptoms of metastatic disease. Men with

localized prostatic tumors will know that, because they

have been confronted with that information by the time

E U R O P E A N U R O L O GY 7 2 ( 2 0 17 ) 9 0 8 9 0 9

available at

www.scienced irect.com

journal homepage:

www.europeanurology.com

DOI of original article:

http://dx.doi.org/10.1016/j.eururo.2017.07.018 .

* Corresponding author. Department of Urology, Erasmus University Medical Centre, P.O. Box 2040, 3000 CA Rotterdam, The Netherlands.

Tel. +31 10 7033607.

E-mail address:

c.h.bangma@erasmusmc.nl

(C. Bangma).

http://dx.doi.org/10.1016/j.eururo.2017.08.003

0302-2838/© 2017 European Association of Urology. Published by Elsevier B.V. All rights reserved.