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while others abandon it, choosing to either undergo

definitive treatment or simply manage their disease with

watchful waiting.

In this issue of

European Urology

, Van Hemelrijck et al

[8]

present results for a Markov model that explores the

outcomes for patients who elected to undergo active

surveillance in Sweden during the past 25 yr. They used

data from multiple registries to assemble a cohort of men

with low-risk prostate cancer and to calculate the

probabilities that these men stayed on active surveillance

or transitioned to another strategy. Their analysis provides

dramatic insights and their figure offers patients visual cues

concerning their likely trajectory.

Their results confirm that approximately 25% of men of

all ages will abandon active surveillance after 2–3 yr of

follow-up. After that there is constant erosion, so that by

10 yr only 25% of men remain on active surveillance.

Younger men are more likely to transition to some type of

definitive treatment, while men older than 70 yr are likely

to abandon active surveillance in favor of watchful waiting.

The recent publication of the PROTECT trial results confirms

these findings

[9] .

Approximately 25% of the men in the

active monitoring arm had abandoned active surveillance

by 3 yr, and 55% had received a radical intervention by 10 yr.

None had transitioned to watchful waiting, since this was

not part of the trial design.

Active surveillance is an appropriate treatment for

many men with low-volume, low-grade prostate cancer.

However, men embarking on this treatment strategy should

recognize that most will transition to an alternative strategy

within a decade. Van Hemelrijck et al have provided men

with an easily understood figure to grasp these concepts.

Clinicians and researchers should seize this insight by

developing active surveillance protocols that extend over

10 yr.

Conflicts of interest:

The author has nothing to disclose.

References

[1]

Siegel RL, Miller KD, Jemal A. Cancer statistics, 2016. CA Cancer J Clin 2016;66:7–30.

[2]

Thompson IM, Goodman PJ, Tangen CM, et al. The influence of finasteride on the development of prostate cancer. N Engl J Med 2003;349:215–24.

[3]

Schroder FH, Hugosson J, Roobol MJ, et al. Prostate-cancer mortality at 11 years of follow-up. N Engl J Med 2012;366:981–90.

[4]

Andriole GL, Crawford ED, Grubb RL, et al. Mortality results from a randomized prostate-cancer screening trial. N Engl J Med 2009;360:1310–9

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[5]

Johansson JE, Andren O, Andersson SO, et al. Natural history of early, localized prostate cancer. JAMA 2004;291:2713–9.

[6]

Albertsen PC, Hanley JA, Fine J. 20-year outcomes following conser- vative management of clinically localized prostate cancer. JAMA 2005;293:2095–101.

[7]

Dall’Era MA, Albertsen PC, Bangma C, et al. Active surveillance for prostate cancer: a systematic review of the literature. Eur Urol 2012;62:976–83

.

[8]

Van Hemelrijck M, Garmo H, Lindhagen L, et al. Quantifying the transition from active surveillance to watchful waiting among men with very low-risk prostate cancer. Eur Urol 2017;72:534–41.

[9]

Hamdy FC, Donovan JL, Lane JA, et al. 10-year outcomes after monitoring, surgery or radiotherapy for localized prostate cancer. N Engl J Med 2016;375:1415–24.

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