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cancer-sparing techniques at the time) and when we

started working on robotic prostatectomy. We personally

did not find any patient who met the Villers’ criteria for

partial prostatectomy when we modeled the operation in

thousands of whole-mount sections from our robotic

prostatectomy tissue bank (Idea, Development, Exploration,

Assessment, Long-term Follow-up

[14_TD$DIFF]

[IDEAL] Stage 0 study).

However, many large specimen banks exist that will allow

independent preclinical simulation of those who may be an

appropriate candidate for a partial prostatectomy. Such

attempts should entail a detailed, retrospective, whole-

mount analysis of the radical prostatectomy samples from

patients who were initially diagnosed to have focal disease

on their biopsy. The final pathology correlation would then

provide an estimate on what proportion of such patients

had truly focal disease versus those that harbored signifi-

cant disease elsewhere in the prostate gland. In our

[15_TD$DIFF]

IDEAL

Stage 0 series (unpublished data), only patients with a

prostate-specific antigen

<

6 ng/dl and who had less than

three foci of cancer in the prostatic base could have been

candidates for partial prostatectomy, as only 6% of such

patients had apical cancer, and none of those apical cancers

were clinically significant.

These preclinical simulation studies may also allow for

the development of stricter inclusion criterias and/or

development of predictive instruments to identify the ideal

candidates for the partial prostatectomy.

For the moment, Villers and colleagues

[1]

should be

congratulated on a fresh, bold way of thinking about

prostate cancer. For the future, we are left wondering, is

partial prostatectomy ready for primetime? Are the

recurrence rates following focal therapy high because

prostate cancer is essentially a multi-focal disease

[

[16_TD$DIFF]

13]

or

is it because current diagnostic methods are not sophisti-

cated enough to detect the index lesion

[

[17_TD$DIFF]

14,15]

? Is adding a

few years of potency worth risking cancer control—what

does a patient want? Or are surgeons the ones being

unsophisticated in their approach to treating many prostate

cancers early?

With continual improvements in nuanced approaches to

prostate cancer, perhaps we will soon say, ‘‘Je le pansai, et il

guerit.’’

Conflicts of interest:

The authors have nothing to disclose.

References

[1]

Villers A, Puech P, Flamand V, et al. Partial prostatectomy for anterior cancer: short-term oncologic and functional outcomes. Eur Urol 2017;72:333–42.

[2]

Begg CB, Riedel ER, Bach PB, et al. Variations in morbidity after radical prostatectomy. N Engl J Med 2002;346:1138–44

.

[3]

Schover LR, Fouladi RT, Warneke CL, et al. Defining sexual outcomes after treatment for localized prostate carcinoma. Cancer 2002;95: 1773–85.

[4

[19_TD$DIFF]

]

Donovan JL, Hamdy FC, Lane JA, et al. Patient-reported outcomes after monitoring, surgery, or radiotherapy for prostate cancer. N Engl J Med 2016, [Epub ahead of print].

[5]

Menon M, Shrivastava A, Kaul S, et al. Vattikuti Institute prostatec- tomy: contemporary technique and analysis of results. Eur Urol 2007;51:648–57.

[

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6]

Ficarra V, Novara G, Ahlering TE, et al. Systematic review and meta- analysis of studies reporting potency rates after robot-assisted radical prostatectomy. Eur Urol 2012;62:418–30.

[

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7] Sood A, Jeong W, Peabody JO, Hemal AK, Menon M. Robot-assisted

radical prostatectomy: inching toward gold standard. Urol Clin

North Am 2014;41:473–84.

http://dx.doi.org/10.1016/j.ucl.2014. 07.002

.

[8]

Hanbury DC, Sethia KK. Erectile function following transurethral prostatectomy. Br J Urol 1995;75:12–3.

[

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9]

Davila HH, Weber T, Burday D, et al. Total or partial prostate sparing cystectomy for invasive bladder cancer: long-term implications on erectile function. BJU Int 2007;100:1026–9.

[

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10]

Ahmed HU, Hindley RG, Dickinson L, et al. Focal therapy for local- ised unifocal and multifocal prostate cancer: a prospective devel- opment study. Lancet Oncol 2012;13:622–32.

[

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11] Hamdy FC, Donovan JL, Lane JA et al., 10-year outcomes after

monitoring, surgery, or radiotherapy for localized prostate cancer.

N Engl J Med. In press.

http://dx.doi.org/10.1056/NEJMoa1606220 .

[

[12_TD$DIFF]

12]

Ahmed HU. The index lesion and the origin of prostate cancer. N Engl J Med 2009;361:1704–6

.

[

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13]

Andreoiu M, Cheng L. Multifocal prostate cancer: biologic, prog- nostic, and therapeutic implications. Hum Pathol 2010;41:781–93

.

[

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14]

Le JD, Stephenson S, Brugger M, et al. Magnetic resonance imaging- ultrasound fusion biopsy for prediction of final prostate pathology. J Urol 2014;192:1367–73.

[15] Liu W, Laitinen S, Khan S, et al. Copy number analysis indicates

monoclonal origin of lethal metastatic prostate cancer. Nat Med

2009;15:559–65.

http://dx.doi.org/10.1038/nm.1944 .

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