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4.

Discussion

In our series of 68 patients undergoing midline EP-RPLND,

we saw a return of bowel function on postoperative day

2 and median LOS of 3 d. There were no cases of ileus.

Notably, 41 patients (60%) were PC, for which 19 (46%) had a

mass

>

10 cm, yet no significant differences in outcomes

were seen between the primary and PC groups. We

postulate that by avoiding entry into the peritoneal cavity,

the risk of paralytic ileus and small bowel obstruction (SBO)

can be minimized, as can risk of injury to intraperitoneal

structures. Preserving the peritoneal sac also minimizes

insensible fluid loss, which is particularly valuable in the PC

bleomycin-treated population, in whom perioperative fluid

management is critical. Overall, our PC LOS represents a

significant difference to that found in a 2016 population-

based analysis of PC-RPLND morbidity, in which 25% of

patients had a hospital stay of

>

7 d (median 9 d)

[6]

.

Because this approach offers excellent exposure, even for

a full bilateral dissection in the setting of large masses, our

lymph node yield was not compromised, with a median of

36 nodes resected. This is in line with contemporary large

series reporting a median of 28–38 nodes resected; yields in

this range have been associated with a higher percentage of

positive nodes found and a lower risk of relapse

[7,8]

. In

addition, nerve sparing was possible in all primary RPLND

patients and 78% of PC patients, with antegrade ejaculation

rates of 91.6% and 97.8%, respectively. This is consistent

with rates reported for recent series

[9]

.

Although RPLND has undergone significant refinements

since the original descriptions, it remains a fairly morbid

procedure for an otherwise healthy, young population

[10,11]

. Even in the primary RPLND setting, Baniel et al

[12]

described an 11% overall postoperative complication rate in

a series of more than 478 patients, the largest such series

reported, including 11 patients (2%) with SBO, of which

eight required emergent laparotomy and lysis of adhesions.

In 2014, Subramanian et al

[13]

described a 24% complica-

tion rate in the primary setting and 32% in the PC setting in

their series of 204 patients at a tertiary center. This included

41 patients with ileus, ranging from a requirement for

bowel rest for at least 6 d to TPN (

n

= 16) and SBO requiring

reoperation (

n

= 1), with an additional two patients requir-

ing this in the long term. Two smaller contemporary cohorts

showed a decline in postoperative complications and

hospital stay over time, but still had LOS of 6 and 4 d,

respectively

[14,15]

. Therefore, there should be a focus on

strategies that minimize perioperative and potentially long-

term complications, and a midline EP approach is an

example with demonstrated results.

Oncologic outcomes were not compromised in our

series. Four patients experienced relapse in the retro-

peritoneum. Three of these had clinical stage IIA embryonal

predominant NSGCT and underwent primary RPLND. The

first, who was a dialysis-dependent diabetic, developed an

in-field recurrence seen on surveillance computed tomog-

raphy; the patient underwent salvage chemotherapy with

resolution of this lesion, then developed lymphadenopathy

in the pelvis, with subsequent pelvic lymphadenectomy

revealing no disease. He was subsequently lost to follow up

but died of unknown causes 8 mo later. The second patient

developed in-field and pulmonary relapses 2 mo after

RPLND, was successfully salvaged with chemotherapy, and

remains disease free. The third patient had a persistent

1-cm mass in the retroperitoneum with negative markers,

but opted for salvage chemotherapy and is disease-free. Our

results are consistent with reported series showing that

30–40% of patients with stage II NSGCT will relapse after

primary RPLND, and that essentially all can be salvaged

successfully with chemotherapy

[16] .

The last patient

underwent RPLND after salvage chemotherapy and was

found to have high-volume teratoma and 2% viable disease

at RPLND. He then had a marker and retroperitoneal relapse

and underwent high-dose chemotherapy with stem cell

transplant and repeat RPLND, and subsequently died of

disseminated disease. This is also unfortunately consistent

with the poorer outcomes associated with RPLND in the

salvage setting

[17]

.

To the best of our knowledge, a midline EP approach for

RPLND has not been described by other groups. It has been

described in the literature on general surgery, particularly to

gain access to the aorta for open abdominal aortic aneurysm

repair

[18–20] ,

with series demonstrating a trend towards

lower rates of ileus and shorter LOS, including one random-

ized controlled trial comparing midline TP versus EP

approaches, although the results in the latter did not reach

statistical significance

[21] .

Almost 20 yr ago, Christmas et al

[22]

reported 80 cases of PC RPLND performed extraper-

itoneally via a thoracoabdominal (

n

= 71) or flank (

n

= 9)

incisionat the level of the12th rib; they achieved full access to

the retroperitoneum and reported no cases of postoperative

ileus. In our experience these incisions are more morbid than

a midline one and are unnecessary for adequate exposure.

Minimally invasive techniques also have the potential to

minimize the surgical morbidity of RPLND and warrant

discussion here. Steiner et al

[23]

described the largest

laparoscopic series to date of 100 PC cases of RPLND for stage

II disease. All but one case was completed laparoscopically

Table 3 – Ejaculatory outcomes for retroperitoneal lymph node

dissection (RPLND)

Primary RPLND PC RPLND

Total cases (

n

)

27

41

Nerve-sparing procedure,

n

(%)

27 (100)

32 (78)

Antegrade ejaculation,

n

(%)

22/24 (91.6)

30/31 (96.8)

Retrograde ejaculation,

n

(%)

2/24 (8.3)

1/31 (3.2)

Missing data (

n

)

3

1

Table 2 – Clavien-Dindo complications at 90 d

Clavien grade

Frequency,

n

(%)

Total (in 11 patients)

12 (17.6)

Grade I

6 (55)

Grade II

5 (45)

Grade IIIa

0

Grade IIIb

1 (1.5)

Grade IV

0

Grade V

0

E U R O P E A N U R O L O G Y 7 2 ( 2 0 1 7 ) 8 1 4 – 8 2 0

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