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Platinum Priority – Editorial

Referring to the article published on pp. 560–567 of this issue

The Role of Lymphadenectomy for Renal Cell Carcinoma:

Are we any Closer to an Answer?

James

[2_TD$DIFF]

R. Porter

*

Swedish Urology Group, Seattle, WA, USA

[1_TD$DIFF]

As a cancer, renal cell carcinoma (RCC) is unique in that it is

relatively resistant to radiotherapy and does not respond to

standard chemotherapy. So when the current study

reported by Gershman et al

[1]

in this month’s issue of

European Urology

found that removal of lymph nodes in

patients undergoing radical nephrectomy had no appreci-

able impact on cancer outcomes, this was in keeping with

the recalcitrant nature of RCC.

The authors retrospectively analyzed 1797 patients

undergoing radical nephrectomy over a 20-yr time frame,

and 606 (34%) underwent a concurrent lymph node

dissection (LND). Importantly, the indications for LND

and the extent of dissection could not be determined and

were at the discretion of the surgeon. Despite the large

cohort and greater than 10-yr median follow-up, perform-

ing LND during radical nephrectomy was not associated

with any improvement in cancer specific mortality or all-

cause mortality.

This same issue was addressed in a prospective manner

by the European Organization for Research and Treatment

of Cancer (EORTC) trial 30881 published in

European

Urology

in 2009

[2] .

The trial compared 389 patients

undergoing radical nephrectomy alone with 383 patients

undergoing radical nephrectomy combined with LND.

Similar to the current study by Gershman et al

[1]

, there

was no difference between the two groups with regard to

overall survival, progression-free survival, or time to

progression of disease. While this is the only randomized

trial to address this issue, concerns have been raised about

EORTC 30881 and its ability to determine the role of LND

during nephrectomy

[3]

. The major limitation of the study is

the relatively low risk of the patients randomized with 70%

of patients either T1 or T2 and many would be candidates

for partial nephrectomy today. In addition, only 4% of

patients undergoing LND were found to have positive nodes

again indicating a low-risk cohort. Because of the many low-

risk patients and the low rate of positive lymph nodes, the

trial was inadequately powered to determine if LND during

nephrectomy is of benefit in patients with RCC.

Both the current study and the EORTC trial found no

oncologic benefit of LND in patients undergoing nephrec-

tomy. Both studies have a relatively low positive node rate

with the current study at 6.2%. One methodologic issue in

the current study that should be noted is that 153 high-risk

patients were excluded from the propensity matching

analysis because there were no suitable matches in the non-

LND group. This could have the effect of lowering the overall

risk of the LND group and make any difference in cancer

outcomes harder to detect.

What the two studies also have in common is that the

boundaries or the extent of the LND are unknown and this

commonality may be important to the reported outcomes.

The extent of lymph nodes removed has become increas-

ingly recognized as an important factor in patients

undergoing LND for bladder and testis cancer. An inade-

quate LND during radical nephrectomy could result in some

patients being reported as N0 when they are really N1, and

they could paradoxically have worse oncologic outcomes

than the patients who did not receive LND.

In fact, a similar finding was identified in a study by

Feuerstein et al

[4] .

In a retrospective review of 258 patients

undergoing cytoreductive nephrectomy, 177 (69%) received

LND and 59 (33%) were found to have positive lymph nodes.

The 5-yr overall survival was 21% for patients undergoing

LND as compared with 31% for patients who did not receive

LND. They found that overall survival was worse for patients

E U R O P E A N U R O L O G Y 7 1 ( 2 0 1 7 ) 5 6 8 – 5 6 9

available at

www.scienced irect.com

journal homepage:

www.europeanurology.com

DOI of original article:

http://dx.doi.org/10.1016/j.eururo.2016.09.019

.

* Swedish Urology Group, 1101 Madison, Suite 1400, Seattle, WA 98104, USA. Tel.+1-206-386-6266; Fax: +1-206-622-1052.

E-mail address:

porter@swedishurology.com . http://dx.doi.org/10.1016/j.eururo.2016.10.028

0302-2838/

#

2016 European Association of Urology. Published by Elsevier B.V. All rights reserved.