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caution, since significant biases related to both the

additional androgen deprivation therapy that was admin-

istered in significant proportions of patients in almost all

reported series and to the different definition of complete

PSA response in the different studies

[4–7]

. When analyzing

the biochemical outcome in patients who had complete PSA

response to surgery, 5 yr after sLND the majority of them

develop a new BCR with a median time of 12–21 mo. In all

available series, the development of a new clinical

recurrence (CR) is delayed, and it is of note that 5 yr after

sLND 25–52% of these patients with established CR before

surgery are actually free from CR. However, the long-term

outcomes of patients treated with sLND have been reported

in a single study that was published in 2015. At a median

follow-up of 81.1 mo, 8-yr CR- and CSM-free survival rates

were 38% and 81%, respectively

[8]

.

3.

For whom?

All studies tried to identify prognostic factors in order to

select the

perfect

candidate to sLND. Complete PSA response

to sLND, the absence of retroperitoneal involvement, PSA

value

<

4.0 ng/ml, and the number of positive nodes has

been demonstrated to be positive-independent prognostic

factors. However, there are conflicting results in terms of

the reported prognostic factors in the different series

[5–8]

.

These conflicting results may be attributable to the limited

numbers of patients included, to the inclusion of patients

with highly variable past history, to the differences in

surgical technique (LND template, surgical approach), as

well as to the nonstandardized use of additional therapies

both before and after sLND.

In 2015, two systematic reviews have analyzed the

outcomes of patients with BCR and lymph nodal recurrence

of PCa

[9,10]

. The main conclusions of these manuscripts

confirm that a metastases-directed treatment is a promis-

ing approach for oligometastatic PCa recurrence, although

high-level evidence studies are currently missing.

Regarding the complications of sLND, it needs to be

acknowledged that the reported Clavien-Dindo IIIA and IIIB

complications are 9.7–17.9% and 0–4.1%, respectively.

These figures are significantly higher than in patients

submitted to LND at the time of radical prostatectomy,

suggesting that this surgery might be demanding. This

needs to be taken into account especially when such an

experimental procedure is proposed.

In the future, the introduction of new tracers for PET/

CT scan will certainly improve the results in terms of

positive lymph node retrieval at surgery and eventually

[1_TD$DIFF]

reduce the need for extensive templates which invariably

increase the morbidity of surgery. However, to date, we

strongly suggest that whenever a sLND is planned, this

should be extensive and must not be limited to the site of

the PET/CT positivity, since additional metastatic lymph

nodes are often found outside the field of imaging

positivity

[3] .

In conclusion, despite the lack of strong evidence, several

studies have shown that sLND might represent a viable

treatment modality for node-only recurrent PCa. However,

as long as high quality data are not available, sLND should

be still considered experimental.

Conflicts of interest:

The authors have nothing to disclose.

References

[1]

Heidenreich A, Bastian PJ, Bellmunt J, et al. EAU guidelines on prostate cancer. part 1: screening, diagnosis, and local treatment with curative intent-update 2013. Eur Urol 2014;65:124–37

.

[2]

van Leeuwen PJ, Stricker P, Hruby G, et al. (68)Ga-PSMA has a high detection rate of prostate cancer recurrence outside the prostatic fossa in patients being considered for salvage radiation treatment. BJU Int 2016;117:732–9

.

[3]

Scattoni V, Picchio M, Suardi N, et al. Detection of lymph-node metastases with integrated [11C]choline PET/CT in patients with PSA failure after radical retropubic prostatectomy: results con- firmed by open pelvic-retroperitoneal lymphadenectomy. Eur Urol 2007;52:423–9.

[4]

Rigatti P, Suardi N, Briganti A, et al. Pelvic/retroperitoneal salvage lymph node dissection for patients treated with radical prostatec- tomy with biochemical recurrence and nodal recurrence detected by [11C]choline positron emission tomography/computed tomog- raphy. Eur Urol 2011;60:935–43.

[5]

Karnes RJ, Murphy CR, Bergstralh EJ, et al. Salvage lymph node dissection for prostate cancer nodal recurrence detected by 11C- choline positron emission tomography/computerized tomography. J Urol 2015;193:111–6.

[6]

Jilg CA, Rischke HC, Reske SN, et al. Salvage lymph node dissection with adjuvant radiotherapy for nodal recurrence of prostate cancer. J Urol 2012;188:2190–7.

[7]

Tilki D, Mandel P, Seeliger F, et al. Salvage lymph node dissection for nodal recurrence of prostate cancer after radical prostatectomy. J Urol 2015;193:484–90.

[8]

Suardi N, Gandaglia G, Gallina A, et al. Long-term outcomes of salvage lymph node dissection for clinically recurrent prostate cancer: results of a single-institution series with a minimum follow-up of 5 years. Eur Urol 2015;67:299–309.

[9]

Ost P, Bossi A, Decaestecker K, et al. Metastasis-directed therapy of regional and distant recurrences after curative treatment of prostate cancer: a systematic review of the literature. Eur Urol 2015;67: 852–63.

[10]

Ploussard G, Almeras C, Briganti A, et al. Management of node only recurrence after primary local treatment for prostate cancer: a systematic review of the literature. J Urol 2015;194:983–8

.

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