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the study design and the analyses presented. Patients with

mRCC might not have been observed for a sufficient time

period to see the occurrence of the outcome. Since the data

capture only in-hospital events, morbidity occurring after

discharge could have not been assessed. Therefore, the rate

of complications might have been underestimated owing

to their possible occurrence outside the observational

period. Moreover, a second problem with this scenario is

that the rate of overall and major complications might

have been significantly different among patients under-

going SM for different types of metastases only because of

different lengths of hospital stay. Furthermore, the lack of

a clear operative definition of overall complications could

have led to the inclusion of complications potentially not

related to SM.

Beyond these considerations, a major limitation associat-

ed with the statistical design of the study is the lack of a

multivariate analysis to assess potential associations be-

tween patient-, hospital-, and disease-related characteristics

and the occurrence of in-hospital complications after SM,

which could have led to potentially spurious associations as

those obtained with univariate logistic regression analysis.

Finally, the results presented also have inherent limita-

tions related to the data sources, such as lack of knowledge

on timing of cytoreductive nephrectomy; administration

(and timing) of possible targeted therapy; number, site,

size, and anatomic accessibility of metastases; synchronous

or metachronous interventions; number of metastases

resected at the time of surgery; patient performance status

at surgery and prognostic risk group; intention to treat

(radical vs palliative); type of surgery; and completeness of

SM. These limitations, alongside the aforementioned sources

of bias, inherently prevent any definitive conclusion

regarding the predictors of in-hospital morbidity after SM,

and therefore any guidance for patient counseling. Thus, we

feel that the conclusions of the authors regarding potential

associations between the occurrence of complications and

patient- or hospital-related characteristics might be poten-

tially inconsistent given the strength of evidence provided.

However, Meyer and colleagues should be praised for

their pioneering efforts to fill the gap in knowledge in this

field, providing reliable data on the rate of complications

after SM for RCC, opening new perspectives, and outlining

the current unmet research needs.

Our view is that current knowledge on the perioperative

morbidity of SM is, as for many other topics in renal cancer

research, just the tip of an iceberg that we are now starting

to realize. Although many unmet needs are likely to remain

unsolved owing to the inherent difficulties in conducting

studies of a high level of evidence in the setting of this

complex disease, the urology community should strive to

improve the quality of future trial design

[8,9]

with the aim

of providing more granular and clinically meaningful

answers to the current controversies.

Conflicts of interest:

The authors have nothing to disclose.

References

[1]

Zaid HB, Parker WP, Safdar NS, et al. Outcomes following complete surgical metastasectomy for patients with metastatic renal cell carcinoma: a systematic review and meta-analysis. J Urol 2017;197: 44–9

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[2]

Capitanio U, Montorsi F. Renal cancer. Lancet 2016;387:894–906

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[3]

Dabestani S, Marconi L, Hofmann F, et al. Local treatments for metastases of renal cell carcinoma: a systematic review. Lancet Oncol 2014;15:e549–61.

[4]

Hanna N, Sun M, Meyer CP, et al. Survival analyses of patients with metastatic renal cancer treated with targeted therapy with or with- out cytoreductive nephrectomy: a National Cancer Data Base study. J Clin Oncol 2016;34:3267–75.

[5] Ljungberg B, Bensalah K, Bex A, et al. EAU Guidelines on renal cell

carcinoma, version. 2016

http://uroweb.org/wp-content/uploads/ EAU-Guidelines-Renal-Cell-Carcinoma-2016.pdf

[6]

Escudier B, Porta C, Schmidinger M, et al. Renal cell carcinoma: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann Oncol 2016;27(Suppl 5):v58–68.

[7]

Meyer CP, Sun M, Karam JA, et al. Complications after metastasect- omy for renal cell carcinoma—a population-based assessment. Eur Urol 2017;72:171–4

.

[8]

Stewart GD, Aitchison M, Bex A, et al. Cytoreductive nephrectomy in the tyrosine kinase inhibitor era: a question that may never be answered. Eur Urol 2017;71:845–7

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[9]

Kamat AM, Sylvester RJ, Bo¨hle A, et al. Definitions, end points, and clinical trial designs for non-muscle-invasive bladder cancer: recom- mendations from the International Bladder Cancer Group. J Clin Oncol 2016;34:1935–44

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