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they choose AS instead of immediate invasive treatment to

avoid overtreatment. It is the predicted overall better QOL

they are choosing

[6]

, and this is exactly the most uncertain

factor in the modeling.

The article suggests introduction of a new paradigm for

personalized tailoring of diagnostic tests and treatment;

this has been argued before for screening and later stages of

the disease, for example

[7] .

The tailoring (ie, adapting the

frequency of PSA testing or switching to active treatment)

will then be based on an individually assessed probability-

based criterion instead of a rule-based criterion. As we still

are unaware of the value of imaging or genomics in risk

assessment, current designs for this type of probability-

based protocol can only be reliably assessed using large data

sets with sufficient events, such as the data compiled in the

GAP3 Movember database initiative with traditional pa-

rameters

[8] .

The actual differences in outcome between AS protocols

and WW appear to be small, as illustrated in the traditional

cohorts mentioned above and the data derived from the

current modeling study. Taking into account the burden of

repeat testing, AS may even look worse than doing nothing

(waiting).

But this is 2017, and we have markers, imaging, and

genomics. In many countries around the world, the

acceptance and reliability of AS are very high and still

increasing (in Scandinavian countries and the Netherlands,

95% of men with low-risk tumors are on AS

[9] )

, which

might partly be a result of offering monitoring technology

and of increasing detection of more low-risk tumors.

Especially for men in their fifth or sixth decade of life,

choice of a WW strategy while on conservative manage-

ment is nonexistent: when informed of the current

diagnostic tests, they all opt for AS. The tradeoff between

more and less intense methods of monitoring only counts

for men aged 65 yr. For those aged

>

75 yr, making a choice

is irrelevant, and one can stop offering or selecting any form

of monitoring. Thus, AS for low-risk prostate cancers is

better than doing nothing, especially for those younger than

65 yr. But doing nothing has already yielded excellent

results, so it remains a challenge how exactly to balance the

benefit of improved clinical outcome versus the harm of

repeat testing.

Most important, however, remains the ability to avoid

diagnosis of low-risk prostate cancers. The harm of

unnecessarily becoming a cancer patient cannot be reversed

by WW or AS.

Conflicts of interest:

The authors have nothing to disclose.

References

[1]

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[2]

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