Abstract
Objective
To conduct a systematic review of comparative studies of laparoscopic nephroureterectomy (LNU), the standard management for upper urothelial tumours, and robot-assisted NU (RANU) that has emerged as a viable alternative.
Methods
MEDLINE, EMBASE and the Cochrane Library were searched according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines to identify all studies reporting on both LNU and RANU for upper urothelial tract tumours.
Results
In all, 1630 patients were included, of which 838 underwent LNU and 792 RANU. Three studies reported on mean operative time and found it to be less in LNU, with two reporting this to be significant (RANU 298 vs LNU 251 min, P = 0.03; 306 vs 234 min, respectively, P < 0.001). Both studies reporting on median node count found this to be higher in the robotic groups: RANU 5.5 vs LNU 1.0 and RANU 21 vs LNU 11. Positive surgical margins (RANU 1.69% vs LNU 7.06%, P = 0.18), bladder recurrence (24.6% vs 36.89%, P = 0.09), and distant metastases (27.50% vs 17.50%, P = 0.29) were not significantly different between the two techniques. Disease-specific mortality did not differ between the two techniques (RANU 7.5% vs LNU 12.5%, P = 0.46), but postoperative mortality was reduced in RANU (0.14% vs 1.32%, P = 0.03). Overall complication rates were statistically lower in RANU, at 12.5% vs 18.8% (P < 0.001).
Conclusions
This review suggests these techniques are equivalent in terms of perioperative and oncological performance. Furthermore, there may be a lower overall complication rate, as well as postoperative mortality in the robotic group. Further research in the form of a randomised controlled trial is warranted.
Abbreviations: CEBM, Centre for Evidence-Based Medicine; EBL, estimated blood loss; LND, lymph node dissection; MeSH, Medical Subject Heading; OT, operative time; PRISMA, Preferred Reporting Items for Systematic Reviews and Meta-Analyses; PSM, positive surgical margins; (L)(RA)NU, (laparoscopic) (robot-assisted) nephroureterectomy; VAS, visual analogue scale
Keywords: Nephroureterectomy, Robotic, Laparoscopic, Ureteric neoplasm ureter
Introduction
Upper urothelial tumours are rare but aggressive tumours and comprise only 5–10% of all urothelial malignancies [1], [2], [3]. The ‘gold standard’ for localised disease is radical nephroureterectomy (NU), with the laparoscopic technique considered the established standard [4], [5]. However, this is still a challenging procedure laparoscopically due to the need for distal ureter dissection and bladder cuff excision. Many centres adopt a combined approach with laparoscopic NU (LNU) and an open ureterectomy and bladder cuff excision [6], [7], [8].
The introduction of robotic surgery with three-dimensional magnified vision and wrist action with a greater degree of freedom has the potential to offer a technically less challenging procedure and better reconstruction of the distal end [9]. Whether this translates into improved oncological or bladder recurrence outcomes are as yet unknown. Current literature on open NU and LNU suggests the technique used for the distal ureter and bladder cuff does not influence bladder recurrence or other oncological outcomes [10].
Therefore, we aimed to conduct a systematic review comparing LNU and robot-assisted NU (RANU) for the efficacy and safety of these two techniques.
Material and methods
The search strategy was conducted in accordance with Cochrane guidelines and the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines [11]. A search strategy was conducted in MEDLINE, EMBASE and the Cochrane electronic databases (from 2000 to present) to identify studies that included both LNU and RANU. The search was conducted using the following keywords; ‘robotic’, ‘robot-assisted’, ‘laparoscopic’, ‘laparoendoscopic’, ‘nephroureterectomy’ and ‘urothelial carcinoma’. Medical Subject Heading (MeSH) phrases included: (‘Ureteral Neoplasms’[MeSH]) AND (‘Laparoscopy’[MeSH]), (‘Ureteral Neoplasms’[Mesh]) AND (‘Robotics’[MeSH]), (‘Ureteral Neoplasms’[MeSH]) AND (‘Robotics’[MeSH]) AND (‘Laparoscopy’[MeSH]).
The list of generated articles was screened by title and abstract by three authors independently (T.S., S-M.L, I.R.) and then relevant full papers were scrutinised. Review articles and bibliographies were also searched to find additional relevant papers. Data were extracted independently by two authors (T.S. and N.S.). A senior author independently (O.A.) cross checked findings to verify end results.
Articles were excluded if the procedure was not performed for a urothelial malignancy, if the patients were aged <18 years, and if the study did not include both LNU and RNU techniques.
The outcomes of interest were; surgical technique, surgical outcomes [e.g. as estimated blood loss (EBL), operative time (OT), lymph node dissection (LND)], oncological outcome [e.g. positive surgical margins (PSM), positive lymph nodes, tumour recurrence, distant metastases], and perioperative outcomes (e.g. hospital length of stay, complications, mortality). Furthermore, we included studies comparing the differences in cost.
Where data were similar a cumulative comparison analysis was conducted to better represent the comparison between the two groups. Each study was assessed for quality in accordance with the Levels of Evidence published by Centre for Evidence-Based Medicine (CEBM), Oxford, UK [12].
Results
Literature search
The search strategy yielded 273 articles, with 259 excluded on the basis of title and/or abstract. The remaining 14 articles were screened, with four identified that met the inclusion criteria (Fig. 1) [9], [13], [14], [15]. This included two matched-comparison studies [9], [13], one cohort study [14], and one population-based study [15]. In all, 1630 patients were included, of which 838 underwent LNU and 792 RANU. The patient characteristics for each study are given in Table 1 [9], [13], [14], [15].
Fig. 1.
PRISMA flowchart of search.
Table 1.
Characteristics of studies included in the systematic review.
| Reference | Country | Number of Institutions | Years data collected | RANU/LNU | No. of patients | Age, years mean (SD) or mean (range) | % Male | Follow-up, months, median (range) | Co-morbidities |
|---|---|---|---|---|---|---|---|---|---|
| Ambani et al. [13] | USA | Single | 2009–2011 | LNU | 22 | 70.8 (2.2) | 72.7 | 15 | Mean (SD) CCI 2.8 (0.5) |
| RANU | 22 | 70.1 (2.2) | 63.6 | 10 | Mean (SD) CCI 2.1 (2.1) | ||||
| P = 0.24 | |||||||||
| Hu et al. [9] | Taiwan | Single | 2011–2013 | LNU | 18 | 69.6 (5.7) | 27.7 | 47.8 (11.9–156.5) | ASA-PS 1 = 0, ASA-PS 2 = 3 (16.7%), ASA-PS 3 = 10 (55.6%), ASA-PS 4 = 2 (11.1%). Hydronephrosis 11 (61.1%), previous abdominal surgery 4 (22.2%), ESRD 2 (11.1%), CKD 16 (88.9%), simultaneous bladder UC 4 (22.2%) |
| RANU | 18 | 70.4 (6.3) | 27.7 | 6.1 (0.6–30.3) | P > 0.05 for all. ASA-PS 1 = 0, ASA-PS 2 = 8 (44.4%), ASA-PS 3 = 6 (33.3%), ASA-PS 4 = 0. Hydronephrosis 12 (66.7%), previous abdominal surgery 5 (27.8%), ESRD 3 (16.7%), CKD 15 (83.3%), simultaneous bladder UC 4 (22.2%) | ||||
| P = 0.646 | |||||||||
| Melquist et al. [14] | USA | Single | 2011–2014 | LNU | 63 | 72.6 (65.8–81.8) | 57.1 | 30.9 (16.1–48.3) | - |
| RANU | 37 | 68.0 (63.6–73.6) | 70.2 | 8.5 (1.8–15.3) | - | ||||
| P = 0.06 | |||||||||
| Trudeau et al. [15] | Canada | Multiple | 2008–2010 | LNU | 735 | 70.6 | 59.9 | - | CCI 0 = 58.1%, 1 = 31.7%, ≥ 2 = 10.2% |
| RANU | 715 | 70.7 | 63.0 | - | CCI 0 = 60.7%, 1 = 31.0%, ≥ 2 = 83% | ||||
| P = 0.951 | P = 0.215 | P = 0.376 |
ASA-PS, American Society of Anesthesiologists Physical Status; CCI, Charlson Comorbidity Index (measure of comorbidity severity and risk of mortality); CKD, chronic kidney disease; ESRD, end-stage renal disease; UC, urothelial cancer.
Of note, one study was excluded as it compared LNU and RANU in a paediatric population [16], and two studies were excluded as case series included LNU and RANU but the individual data for each were not extractable [17], [18]. The remaining seven studies excluded did not compare or report on LNU and RANU, but reported case series of one procedure or the other, or review papers. No randomised controlled trials were identified.
Three studies compared between the two procedures with significant heterogeneity on reporting outcomes, and one study looked at cost comparison. Where possible a cumulative comparative analysis was done.
Surgical outcomes
Table 2, Table 3, Table 4 summarise the findings of the review.
Table 2.
Operative details of studies included in the systematic review.
| Reference | LNU/RANU | Approach | Position | LNU approach for distal ureter | No. of ports | Tumours location, n (%) | Pathological status, n (%) | Chemo, n (%) | OT, min, mean (SD) or mean (range) | EBL, mL, mean (SD) or mean (range) | PSM, n (%) | Node count, median (IQR) | Positive nodes, n (%) |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Ambani et al. [13] | LNU | Low lithotomy + partial flank position (60° to table) | Lap or hand-assisted. Bladder cuff excision endoscopic 14 patients, open 6 patients. | – | 14 renal, 6 ureter: 3 proximal, 3 distal, 2 mixed | T0, 1 Tis, 1 Ta, 6 T1, 4 T2, 2 T3N0, 6 T3N2, 2 |
0 (0) | 251 (14) | 233 (27) | 1 (5) | 1.0 | 2 (29) | |
| RANU | N/a | – | 14 renal, 6 ureter:1 proximal, 5 distal, 2 mixed | T0, 1 Tis, 1 Ta, 6 T1, 4 T2, 2 T3N0, 6 T3N2, 2 |
3 (14) neoadjuvant | 298 (12) | 380 (42) | 2 (9) | 5.5 | 2 (17) | |||
| P = 0.03 | P = 0.02 | P = 0.56 | |||||||||||
| Hu et al. 2015 [9] | LNU | 7-cm Gibson incision for hand port | Hand-assisted | – | 10 renal 5 ureter 3 mixed |
Ta, 7 (38.9) T1, 2 (11.1) T2, 2(11.1) T3, 7 (38.9) N0, 16 (88.9)N1, 2 (11.1) |
– | 250.17 (140–410) | 358.33 (50–2000) | – | – | – | |
| RANU | Robot re-docked after nephrectomy. Patient not repositioned. | Lateral flank position (diseased side up) | N/a | 5 | 10 renal5 ureter3 mixed | Ta, 3 (16.7)T1, 5 (27.8)T2, 6 (33.3)T3, 4 (22.2)N0, 17 (94.4)N1, 1(5.56) | – | 255.17 (110–540) | 68.89 (10–350) | – | – | – | |
| P = 0.333 | P < 0.001 | ||||||||||||
| Melquist et al. 2016 [14] | LNU | Transperitoneal for dissection kidney/ureter/LN. | Extraperitoneal via Gibson excision | – | 29 renal (46)23 ureter (37)11 mixed (17) | T0 = 6Tis, 3 (5)Ta, 16 (25)T1, 10 (16)T2, 8 (13)T3/4, 20 (32) | 34 (54) neoadjuvant | 234 (204–288) | 200 (125–375) | 4 (6) | 11 (5.5–21) | 13 (21) | |
| RANU | Robot over patient hip at 45°, facing contralateral shoulder. | N/a | 5 | 21 renal (57)9 ureter (24)19 mixed (51) | T0, 5Tis, 2 (5)Ta, 9 (24)T1, 12 (32)T2, 2 (5)pT3/4, 7 (19) | 19 (51) neoadjuvant | 306 (234–354) | 150 (100–300) | 0 (0) | 21 (16–30) | 2 (5) | ||
| P > 0.05 | P > 0.05 | P > 0.05 | P < 0.001 | P = 013 | P = 0.29 |
Chemo, chemotherapy; IQR, interquartile range.
Table 3.
Postoperative outcomes of studies included in the systematic review.
| Study | LNU/RANU | Hospital stay, days | Other information | Complications, n (%) | Transfusion rate, n (%) | Follow-up, months | Mortality, n (%) | Intravesical recurrence, n/N (%) | Local recurrence, n (%) | Distant metastasis, n (%) | Disease free at follow-up, n (%) |
|---|---|---|---|---|---|---|---|---|---|---|---|
| Ambani et al. 2014 [13] | LNU | 3.1 | – | 1 intraoperative (not stated) Clavien I, 2 Clavien II, 2 Clavien IIIb, 1 (fascial dehiscence of hand port site requiring surgical intervention) |
0 (0) | 15 | Overall, 2 (9.1) Cancer specific, 2 (9.1) |
7/19 (37), 2 had previously had cystectomy | 5 (23) | 16 (73) | |
| RANU | 3.1 | – | 1 intraoperative (haemorrhage requiring transfusion) Clavien I, 4 Clavien II, 2 Clavien IIIb, 0 Clavien V, 1 postop. death due to haematemesis after discharge |
2 (9.1) | 10 | Overall, 4 (18) Cancer specific, 2 (9.1) | 8/24 (36) | 7 (32) | 11 (52) | ||
| P = 0.93 | P = 0.41 | P = 0.08 | |||||||||
| Hu et al. 2015 [9] | LNU | 9.61 (3–6) | Ileus 0/resumption oral intake 2.17 (1–3) days/VAS pain score 3.93 (3–6) | – | – | 47.8 (11.9–156.5) | Overall, 5 (27.8) Cancer specific, 3 (16.7) |
6 (33.3) | Renal fossa 2 (11.1) | 2 (11.1) | - |
| RANU | 6.22 (3–10) | Ileus 0/resumption oral intake 1.59 (0.5–3) days/VAS pain score 6.22 (3–10) | – | – | 6.1 (0.6–30.3) | Overall, 2 (11.1) Cancer specific, 1 (5.6) |
2 (11.1) | 0 (0) | 4 (22.2) | - | |
| P = 0.043 | P > 0.05/P = 0.043/P = 0.043 | P = 0.781/P = 0.729 | P = 0.849 | P = 0.093 | |||||||
| Melquist et al. 2016 [14] | LNU | 3 (2.5–4) | – | Clavien II, 12 (19) Clavien IIIa, 1 (2) Clavien IIIb, 1 (2) Clavien IVa, 1 (2) |
19 (30) | 30.9 (16.1–48.3) | – | 25 (40) | DSS (94) at 1 year | ||
| RANU | 5 (4.6–6.3) | – | Clavien II, 1 (3) Clavien IIIa, 0 (0) Clavien IIIb, 2 (5) Clavien IVa, 2 (5). |
3 (8) | 8.5 (1.8–15.3) | – | 9 (24) | DSS (94) at 1 year | |||
| P > 0.05 | P = 0.012 | ||||||||||
| Trudeau et al. 2014 [15] | LNU | 5.83 | Overall complications (18.2) | 104 (14.1) | In-hospital mortality (1.4) | ||||||
| RANU | 5.7 | Overall complications (11.9) | 93 (13.0) | In-hospital mortality (0) | |||||||
| P > 0.05 | P < 0.001 | P > 0.05 | P = 0.002 |
DSS, disease-specific survival; Clavien, Clavien-Dindo classification of complications.
Table 4.
Cumulative comparison analysis.
| Outcome | RANU, n/N | LNU, n/N | P |
|---|---|---|---|
| Overall complications | 97/774 | 154/820 | < 0.001 |
| Clavien–Dindo complications | |||
| I | 4/59 | 2/85 | 0.21 |
| II | 3/59 | 14/85 | 0.05 |
| III | 2/59 | 3/85 | 0.96 |
| IV | 2/59 | 1/85 | 0.38 |
| V | 1/59 | 0/85 | 0.20 |
| PSM | 1/59 | 6/85 | 0.18 |
| Follow-up median range across studies, months | 6–30 | 12–48 | |
| Bladder recurrence | 19/77 | 38/103 | 0.09 |
| Distant metastasis | 11/40 | 7/40 | 0.29 |
| Disease-specific mortality | 3/40 | 5/40 | 0.46 |
| Overall survival | 69/77 | 92/103 | 0.95 |
| Postoperative mortality (in-hospital death) | 1/737 | 10/757 | 0.03 |
OT
All three studies found the mean OT to be less for LNU [9], [13], [14], with two reporting this to be statistically significant [13], [14].
EBL
Ambani et al. [13] found LNU to have significantly less EBL. While the remaining two studies found a lesser EBL with RANU [9], [14], with Hu et al. [9] finding this to be statistically significant.
PSM rate
There was no difference between the two groups for PSM rates. Ambani et al. [13] and Melquist et al. [14] found LNU PSM rates of 5% and 6%, respectively; and RANU PSM rates of 9% and 0%, respectively. Neither found the difference to be statistically significant. Cumulative analysis found no difference between the two groups.
LND
The median node count was found to be higher in RANU in both studies that recorded this (5.5 vs 1.0 in Ambani et al. [13]; 21 vs 11 in Melquist et al. [14]). The positive node count was also higher in RANU (29% vs 17% in Ambani et al. [13]; 21% vs 5% in Melquist et al. [14]).
Postoperative complications
Postoperative outcomes were reported heterogeneously across the four studies.
Ambani et al. [13] and Melquist et al. [14] used the Clavien–Dindo classification system. These studies found minor complications (Clavien-Dindo grade ≤ III) to be 18.2% and 19% in LNU, and 27.2% and 3% in RANU. For major complications, Ambani et al. [13] reported one Clavien–Dindo grade ≥ IIIa in the LNU group (a fascial dehiscence of the hand port site). Melquist et al. [14] reported a major complication rate of 4.7% in LNU vs 7.0% in RANU (P > 0.05).
Hu et al. [9] did not report Clavien–Dindo complications, but found a faster return to oral intake after RANU compared with LNU (1.59 vs 2.17 days, P = 0.043), but there was an improved visual analogue scale (VAS) pain score in LNU (3.93 vs 6.22, P = 0.043).
Trudeau et al. [15], in the largest reported series, reported a significantly lower overall complication rate in RANU (11.9% vs 18.2%, P < 0.001).
Overall complication rates were statistically lower in the RANU group (12.5%) vs the LNU group (18.8%) (P < 0.001). However, subclassifying complications to Clavien–Dindo classification yielded no difference between the two groups.
Mortality
Trudeau et al. [15] reported a significant increase in in-hospital mortality in the LNU group (1.4% vs 0.0%, P = 0.002). While Ambani et al. [13] had one postoperative death in the RANU group. A cumulative analysis found postoperative death rates to be statistically less in the RANU group (Table 4) (P = 0.03).
Oncological outcomes
Hu et al. [9] reported better overall and cancer-specific survival in LNU; however this was not statistically significance (overall 27.8% vs 11.1%, P = 0.781; cancer-specific 16.7% vs 5.6%, P = 0.729). Melquist et al. [14] found no difference in disease-specific survival at 1 year (94% vs 94%). Ambani et al. [13] found overall mortality was higher in the RANU group (18% vs 9.1%), but cancer-specific mortality was the same across the groups (9.1% vs 9.1%).
There was no statistically significant difference between the groups for bladder recurrences (P = 0.09), at 24.7% in the RANU group vs 36.9% in the LNU group, despite the slight increase in the LNU group [9], [13], [14].
Local recurrence was only reported in one study, which found no cases in the RANU group but two (11.1%) in LNU group, both recurrences were found in the renal fossa [14].
There was a trend towards a higher rate of distant metastases in the RANU groups (27.5%) vs the LNU groups (17.5%); however, this was not statistically significant (P = 0.29) [9], [13].
Ambani et al. [13] reported on disease-free survival and found a trend favouring LNU over RANU at a median follow-up of 15 months and 10 months, respectively (73% vs 52%, P = 0.08).
Cost
Trudeau et al. [15] reported on comparative costs, in their USA-based study. They found the mean cost to be significantly higher in RANU ($23 235 vs $17 637, P < 0.001).
Quality assessment of studies
The general quality of the studies was poor, with no randomised trials included. The three comparative trials and the population-based study were all retrospective in nature. This included two level 2b studies [14], [15], and two level 3b studies [9], [13], according to the CEBM levels of evidence [12].
Discussion
Overall summary
Although the RANU is emerging, this is the first systematic review to evaluate the outcomes of comparative studies between LNU and RANU. Minimally invasive NU has become increasingly popular, with reported improved perioperative outcomes and comparable oncological results to open NU [10]. However, there remains a paucity of good data available in the literature. There is currently no randomised controlled trial Level 1 evidence, and as found in the present review a paucity of data comparing LNU and RANU. With this is in mind, the present evidence suggests that these two techniques are currently equivocal in terms of perioperative and oncological performance for this technique; however, there seems to be lower overall complication rates, as well as postoperative mortality in the RANU group.
Operative outcomes
All the studies reporting on OTs found them to be higher in RANU cases [9], [13], [14]. However, the data reported by Ambani et al. [13] represent their initial experience with the robot for this procedure, while Melquist et al. [14] performed more complete LNDs in their RANU cases. Furthermore, Ambani et al. [13] and Hu et al. [9] ‘re-docked’ the robot during their procedure, which Melquist et al. [14], in the more recent paper, showed to be avoidable step. Indeed, in published RANU case series in which the patient or robot are not repositioned the mean OT is consistently <200 min [19], [20], [21], while in those studies that re-docked the mean OTs were in concordance with those seen here at ∼300 min [22], [23].
EBL was reduced in RANU in two papers [9], [14], with Hu et al. [9] finding this to be significant (358.33 vs 68.89 mL, P < 0.001). Ambani et al. [13] found a trend towards higher EBL and transfusion rates in RANU patients, but again this was attributed to a learning-curve effect, and their results do not reflect other published RANU series, such as Hemal et al. [20] and Lee et al. [21], who reported an EBL of 103 and 99 mL, respectively. Melquist et al. [14] reported a significantly lower transfusion rates in RANU (8% vs 30%, P = 0.012) and this trend was supported in the largest study in the literature (13.0% vs 14.1%, p > 0.05) [15].
LND should be performed in all patients with ≥T2 tumours, with radiologically or operative lymph node enlargements, it provides key diagnostic information and may be curative in patients with either known limited nodal spread or unseen metastases [24]. Melquist et al. [14] performed a retrospective cohort study with the primary outcome to assess LND in LNU and RANU. That paper, and Hu et al. [9], found RANU to yield a higher median lymph node count. In both cases LNU had a higher positive node count.
Taken together, these findings suggest that with experience and the adoption of RANU without repositioning or re-docking, that RANU could become a more efficient technique in terms of OT and EBL, and a more effective procedure in terms of ability to yield lymph nodes as required.
Complications and mortality
Overall complications were higher in LNU in all but one study [13]. Trudeau et al. [15] found no significant difference in postoperative length of stay; however, overall complications were reduced from 18.2% to 11.9% in RANU procedures (P < 0.001). No other series reported a significant difference in complication rates. This was reflective in the cumulative analysis, whereby the RANU group had less complications overall, but is heavily weighed by the large Trudeau et al. [15] study.
Mortality rates were reportedly inconsistently across the studies. In the largest series, there is a significantly increased in-hospital mortality in LNU (1.4% vs 0%, P = 0.002) [15]. The other two studies that reported on mortality found no significant difference in both overall and cancer-specific mortality [9], [13].
Oncological outcomes
Bladder recurrence rates ranged from 33 to 40% in LNU, which was in agreement with the range of 19–43% reported in a meta-analysis by Ribal et al. [25]. Recurrence rates in RANU cases reported here ranged from 11% to 36%. Lim et al. [26], in a cumulative analysis of RANU series, reported a recurrence rate of 0–44.4%. Although no statistically significant difference was found, there is a suggestion of a trend towards improved recurrence rates with RANU. The ‘gold standard’ for bladder cuff excision is extravesical or transvesical excision of the distal ureter; Lim et al. [26] hypothesised that the technical challenge this poses laparoscopically, in comparison to more advanced dexterity offered by robotics may explain the trend towards improved recurrence rates.
Local recurrences are considered rare after NU, with rates of 4–15% in LNU, and 2.4% in a pooled analysis of RANU [26]. Only one study in the present series reported on local recurrence, finding a rate of 0% in RANU compared with 11.1% in LNU [14]. These should be interpreted with caution given the small sample size, but suggest that local recurrence rates are at least comparable between the two techniques.
Both studies reporting distant metastases found a trend towards improved rates in LNU, although neither found significance [9], [13]. In RANU, Ambani et al. [13] reported a recurrence rate of 32% and Hu et al. [9] reported a recurrence rate of 22%. In a meta-analysis by Rai et al. [10] the pooled rate of distant metastasis for LNU across 16 studies was found to be 11.0%, and 14.7% in open NU.
Cost
Concern over cost in robotics is often raised. Trudeau et al. [15] reported RANU to be a more costly procedure ($17 637 vs $23 235, P < 0.001). However, the generalisability of this to other populations is questionable. Furthermore as robotics continues to increase in popularity and availability of equipment these costs are likely to decrease.
Limitations
Firm conclusions from the available literature are limited in three of the studies by small cohort sizes [9], [13], [14]. In the Trudeau et al. [15] study, although large, it is a population-based study and so should be interpreted with caution. Secondly, the quality of evidence is low, with all available data from retrospective studies with no randomisation, which has an inherent risk of bias. Thirdly, all the studies reviewed use different techniques in both LNU and RANU cases, this again makes them hard to interpret and compare fairly. With all results reported differently between the studies. Finally, there is a limited follow-up period, in particular in RANU with the longest follow-up being only 10 months [13], this makes meaningful interpretation of oncological and survival outcomes difficult.
Implications for practice and research
The available literature suggests outcomes from RANU are at least comparable to LNU; however, firmer conclusions cannot be made given the limitations discussed. Results from other case series suggest that with increased experience RANU may provide favourable performance in terms of OT, EBL, complications, and mortality [19], [20], [21]. Furthermore, both Hu et al. [9] and Melquist et al. [14] report increased lymph node yield, which is an added benefit of RANU indicating that this is an option and is comparable with open surgery.
The present review supports the continued use of both techniques with equipoise. Further research should look to address the limitations discussed – preferably in the form of a large randomised controlled trial. Given the rarity of upper urothelial tumours this may be hard to achieve in a single institution and may need a multi-institutional, multi-national study.
Conclusions
Despite the paucity of current comparative evidence on RANU and LNU, the present systematic review suggests they are equivalent in terms of perioperative and oncological performance. Furthermore, there may be a lower overall complication rate, as well as postoperative mortality in the RANU group. We await further comparative data to add to this field, preferably in the form of a randomised controlled trial, which would be appropriate.
Conflicts of interest
None.
Acknowledgement
Mr Omar M. Aboumarzouk would like to thank Dr Isra Ahsi for her support.
Laparoscopy/Robotics
Footnotes
Peer review under responsibility of Arab Association of Urology.
References
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