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Page Background

Radical cystectomy with extended pelvic lymph node

dissection (PLND) provides the best chance of long-term

survival for clinically localised muscle-invasive bladder

cancer and high-grade recurrent noninvasive disease

[1]

.

However, curative surgery remains challenging, with recur-

rence rates of 30–40% reported within 5 yr of surgery

[2]

.

Recurrences often occur early; more than 80% occur within

the first 2 yr after surgery, with average presentation

occurring 10–15 mo after radical cystectomy

[3]

.

Debate remains as to whether minimally invasive

surgery negatively impacts survival outcomes due to

inadequate resection, suboptimal lymph node dissection,

or alteration of recurrence patterns due to tumour seeding

related to pneumoperitoneum or insufflation

[4] .

A recent

single-centre study compared open radical cystectomy

(ORC) with robot-assisted radical cystectomy (RARC) and

reported a similar incidence of overall transitional cell

carcinoma (TCC) recurrences, with a higher frequency of

peritoneal carcinomatosis and extraperitoneal lymph node

recurrences among patients undergoing RARC

[4]

.

It is recognised in ORC series that early recurrence is an

indicator of poor prognosis that correlates closely with 5-yr

recurrence-free survival (RFS) and overall survival

[5] .

The

current evidence for long-term outcomes following RARC

shows acceptable oncologic outcomes comparable to open

series

[2]

. A multicentre study analysing data for 702 RARC

patients with a minimum of 5-yr follow-up (median 67 mo)

reported 5-yr RFS of 67%.

In the European Association of Urology Robotic Urology

Section (ERUS) Scientific Working Group database,

717 patients at nine different institutions were identified

who underwent totally intracorporeal RARC between

December 2003 and March 2015. The follow-up protocol

comprised history, physical examination, urine cytology,

and laboratory measurements according to EAU guidelines.

Diagnostic imaging was routinely performed at 4–6 mo for

the first year, and at least annually thereafter, or more

frequently when clinically indicated. The median follow-up

was 31 mo (interquartile range [IQR] 20–46).

Patient demographics and oncologic outcomes are

summarised in

Table 1

. Thirty-four patients (4.8%) had a

positive surgical margin (PSM), of whom 31 (4.4%) had pT3/

T4 disease. Three patients (0.4%) with organ-confined

disease had a PSM. The median yield for extended PLND

was 18 (IQR 13–25). Kaplan-Meier estimates were created

for local and distant recurrence sites

( Table 2 )

. RFS at 3, 12,

and 24 mo was 95.9%, 80.2%, and 74.6% respectively

(Supplementary Fig. 1). Univariable and multivariable Cox

regression was used to estimate hazard ratios for predictors

of RFS (Supplementary material).

We observed early recurrences at any site in 4.1% of

patients at 3mo, 19.8% at 12mo, and 25.4% at 24mo, similar

to rates seen in ORC series

[5–7] .

Distant recurrences were

most frequent in the bones, lungs, and liver, while local

recurrences were most common in pelvic lymph nodes.

This is consistent with recurrence patterns seen in ORC and

in autopsy series

[6,7]

. Regarding unusual recurrence

patterns

[4]

, five patients (0.7%) had peritoneal carcino-

matosis and two patients (0.3%) had metastasis at the port

site (wound site), which are both of low incidence and

consistent with published ORC series

[7]

. In a recent

review, RFS rates at 2 yr after surgery ranged from 67% to

81% in RARC series

[8]

, and studies highlighting unusual

recurrence patterns as a possible indicator of a detrimental

effect have not shown a higher incidence of recurrences

compared to ORC performed in the same institution

[4]

.

It has been found at autopsy that peritoneal carcinoma-

tosis incidence is as high as 19% among bladder cancer

patients, but importantly it is most frequently associated

with extensive metastases at multiple sites

[6] .

Review of

the patients in our series with peritoneal carcinomatosis

and port-site metastasis revealed that all had high-grade

Table 1 – Patient demographics and oncologic outcomes

Variable

Result

Patients (n)

717

Male/female (

n

)

78/22

Median age, yr (IQR)

68 (62–74)

ASA grade (

n

)

1

17

2

51

3

31

4

1

Median BMI, kg/m

2

(IQR)

26 (23–28)

Median follow-up, mo (IQR)

31 (20–46)

Histology,

n

(%)

Transitional cell carcinoma

680 (95.2)

Squamous cell carcinoma

20 (2.8)

Adenocarcinoma

9 (1.2)

Neuroendocrine

2 (0.3)

Small cell carcinoma

3 (0.4)

Missing data

3

Preoperative staging,

n

(%)

Carcinoma in situ

34 (4.8)

Ta

25 (3.5)

T1

154 (21.6)

T2

370 (52.0)

T3

76 (10.7)

T4

19 (2.7)

Non–transitional cell carcinoma

34 (4.8)

Missing data

5

Received neoadjuvant chemotherapy,

n

(%)

176 (25.2)

Missing data

19

Pathological stage (%)

pT0

136 (19.1)

pTis

76 (10.7)

pTa

34 (4.8)

pT1

72 (10.1)

pT2

162 (22.7)

pT3

163 (22.9)

pT4

69 (9.7)

Missing data

5

Soft tissue margin positive,

n

(%)

34 (4.8)

Missing data

2

PLND template,

n

(%)

No PLND

35 (5.1)

Standard

144 (20.8)

Extended PLND

518 (74.3)

Missing

20

Pathologic nodal stage,

n

(%)

Nx

35 (4.9)

N0

548 (77.1)

N1

58 (8.2)

N2

70 (9.8)

Missing

6

PLND = pelvic lymph node dissection.

E U R O P E A N U R O L O G Y 7 1 ( 2 0 1 7 ) 7 2 3 – 7 2 6

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