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SYMPOSIUM
Year : 2013  |  Volume : 29  |  Issue : 4  |  Page : 338-344
 

Bladder neck sparing in radical prostatectomy


Department of Urology, Stepping Hill Hospital, Stockport, United Kingdom

Date of Web Publication21-Oct-2013

Correspondence Address:
Michal Smolski
9 Goodwood Road, Marple, Stockport, SK6 7QW
United Kingdom
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/0970-1591.120118

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   Abstract 

The role of a bladder neck sparing (BNS) technique in radical prostatectomy (RP) remains controversial. The potential advantages of improved functional recovery must be weighed against oncological outcomes. We performed a literature review to evaluate the current knowledge regarding oncological and functional outcomes of BNS and bladder neck reconstruction (BNr) in RP. A systematic literature review using on-line medical databases was performed. A total of 33 papers were identified evaluating the use of BNS in open, laparoscopic and robotic-assisted RP. The majority were retrospective case series, with only one prospective, randomised, blinded study identified. The majority of papers reported no significant difference in oncological outcomes using a BNS or BNr technique, regardless of the surgical technique employed. Quoted positive surgical margin rates ranged from 6% to 32%. Early urinary continence (UC) rates were ranged from 36% to 100% at 1 month, with long-term UC rate reported at 84-100% at 12 months if the bladder neck (BN) was spared. BNS has been shown to improve early return of UC and long-term UC without compromising oncological outcomes. Anastomotic stricture rate is also lower when using a BNS technique.


Keywords: Bladder neck reconstruction, bladder neck sparing, lissosphincter, radical prostatectomy, rhabdosphincter


How to cite this article:
Smolski M, Esler RC, Turo R, Collins GN, Oakley N, Brough R. Bladder neck sparing in radical prostatectomy. Indian J Urol 2013;29:338-44

How to cite this URL:
Smolski M, Esler RC, Turo R, Collins GN, Oakley N, Brough R. Bladder neck sparing in radical prostatectomy. Indian J Urol [serial online] 2013 [cited 2019 Sep 22];29:338-44. Available from: http://www.indianjurol.com/text.asp?2013/29/4/338/120118



   Introduction Top


'The three goals of radical prostatectomy (. . .) are cancer control, preservation of urinary control, and preservation of sexual function'. [1] As the techniques of RP have evolved, our understanding of the relevant anatomy has improved and better oncological and functional outcomes have been reported. Despite this, there remains no consensus on operative technique and there remain many technical components of the procedure itself where controversy exists. One such contentious area is the role of bladder neck sparing (BNS) versus bladder neck reconstruction (BNr) and the impact of both techniques on oncological and functional outcomes. Those in favour of BNS suggest this technique allows earlier return of continence and a lower incidence of post-operative strictures, without compromising oncological clearance. [2] Surgeons who favour BNr state concerns about compromising surgical margins with no definitive improvement in functional outcome. [3] BNS has been incorporated into open RP (ORP), laparoscopic RP (LRP) and robot-assisted laparoscopic prostatectomy (RALP) techniques. Technical aspects of BNS vary between the surgical approaches because of the technical difficulties this can present and the prolonged learning curve. [4],[5],[6] Circumferential, anterior and lateral approaches to the have all been described in ORP, LRP and RALP. [7],[8],[9],[10],[11],[12]

Improved surgical techniques and appreciation of the local anatomy have seen huge modifications to the technique of RP since the first described procedure by Proust in 1901. [13] Preservation of the neurovascular bundle was first reported in 1983 by Walsh et al. and since then, sparing of suspensory mechanism of the urethra [11],[14] preservation of urethral length [15],[16] posterior rhabdosphincter sparing, [17] BNS [18] and seminal vesicle sparing [19] have all been described as important techniques for optimising functional outcome after RP. BNS has evolved from a better understanding of the anatomy and physiology of mechanisms of UC. New research based on embryological, 3D imaging and urodynamic studies have redefined our understanding of the urinary sphincter mechanism. We now understand the contributions of the BN as an integral part of larger, complex sphincter mechanism that consists of both striated and smooth muscle fibres, [20] rather than an independent external (rhabdo) and internal (lisso) sphincter as previously thought. The rhabdosphincter is horseshoe-shaped and overlies the circular and longitudinal smooth muscle of the urethra. During periods of increased intra-abdominal pressures it contracts and coapts the urethra. [20],[21] Due to the relatively low volume of slow twitch muscle fibres compression of the rhabdosphinter cannot be sustained for longer than about 60 s. [21] During the storage phase, the lissosphincter maintains urethral resistance and is the primary mechanism responsible for maintaining resting and baseline continence. Urodynamics studies have demonstrated that an intact lissosphincter maintains continence in the absence of a viable rhabdosphincter. [20],[22] BNS technique aims to leave most of the lissosphincter mechanism intact allowing preservation of its function.

We performed a search of the PubMed, Science Direct and Wiley library databases to identify original and review articles in English which addressed BNS and BN reconstruction techniques, oncological and functional outcomes of ORP, LRP and RALP, where BNS technique was used. The search terms used were BN, spare, preservation, reconstruction, urinary incontinence, positive margin, ORP, LRP and RALP. Abstracts and reports from meetings were not included. Relevant articles were reviewed, analyzed and summarized in line with the intentions of this review article. Our initial online database search returned 345 results; 133 via Science Direct, 122 via PubMed and 90 via Wiley library. We further evaluated significant articles found in the citation lists. After narrowing the search down to the relevant papers, current review included 12,806 patients in 31 original studies plus further two review articles directly pertinent to the topic of BNS and BNr. There are 19 studies describing outcomes of BNS in ORP included in the review, six studies on BNS in LRP and five original articles on outcomes of BNS in RALP. The only prospective, randomised study included patients undergoing both RALP and ORP (level of evidence 1b). Remaining studies are non-randomised prospective and retrospective studies with varying population size sample (level of evidence 2-4).

Oncological outcomes

The relationship between BNS and positive surgical margin (PSM) is well-documented in the literature [Table 1]. However, only one study is a prospective, randomised, blinded study with a control group. [18] Gomez et al. in a prospective study did not find any sole PSM at BN in the cohort of 50 men undergoing ORP and BNS, although there were six patients (12%) who had multiple positive margins involving BN. [23] Wood et al. and Lepor et al. performed studies involving intraoperative biopsies of the BN after BNS. [24],[25] Wood demonstrated that all nine patients (12%) who had PSM at the BN had multiple PSM's and T3 disease. This was confirmed further by Braslis et al., Soloway and Neulander. [26],[27] Braslis et al. reported there was no sole PSM at BN after ORP and 7.5% patients had PSM at the BN, which were multiple PSM's. [26] Soloway and Neulander found only 1% sole PSM at BN. In his study of 676 patients, 4.3% patients had multiple PSM also involving BN. [27] In the series of 365 patients undergoing ORP Shelfo et al. reported total PSM rate at 32%, but only two patients had sole BN PSM. [28] Similarly, Poon et al. in the retrospective cohort study of 220 men concluded no statistical difference between patients undergoing BNS versus the control group. [2] As described by Bianco et al. in the larger prospective studies of 555 men undergoing ORP, total PSM was 32% with 13% PSM at BN and 0.36% sole PSM at BN. [29] More recently Freire et al., in a series of 619 men undergoing RALP, assessed PSM rate at the base of the prostate in the BNS versus control group. [30] Rates were 1.4% and 2.2% respectively. Similarly, Friedlander et al. in a retrospective evaluation of a large cohort of over 1000 men demonstrated identical PSM for BNS and control group, which was 13.8%. [31] In a new prospective, randomised, controlled and blinded study from the Heidelberg group, only 2% of BNS group had a sole PSM at the BN compared with 12.5% PSM rate in the control group. [18] Contrary to the above, Srougi et al. published results of their prospective study, where they ceased recruitment after 70 patients as the PSM rate was 10%, all being at the BN irrespective of the group. [3] In LRP, Katz et al. published results of the series, where overall PSM was 26% and PSM at BN as 9.75%. [32] During the study, they abandoned BNS approach and decreased PSM at BN to zero. Several studies stressed that appropriate patient selection is crucial in order not to compromise the surgical outcome. [12],[28],[33],[34],[35]
Table 1: Oncological outcomes of BNS

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High Gleason score on the prostatic biopsies or suspicion of extra-prostatic extension increases the risk of PSM at the BN. [12],[28],[35] Aydin et al. described the significance of a sole PSM at the BN. [36] In his retrospective study of 164 men with PSM after ORP, 23% had sole PSM at the BN. Those patients had 69.8% 5-year actuarial risk of biochemical progression compared with 33% who had negative BN margin. The data highlights that the presence of a PSM at the BN has a significant impact on long-term outcomes. Both Marcovich et al. and Aydin et al. have found that a PSM at the BN results in higher rates of biochemical recurrence when compared with single or multiple PSM at other sites. [35],[36] However, in 2010, Pierorazio et al. published the results of large review on over 17,000 patients. [37] PSM rate at the BN was only 1.2%. Patients with an isolated PSM at the BN had prostate specific antigen (PSA) free survival rate of 37% and cancer free survival of 92%, which was comparable to prognosis of patients with a seminal vesicle invasion and an extracapsular extension respectively. They concluded that American Joint Committee on Cancer should reconsider BN involvement staging as T4.

Assessing long-term oncological outcomes, we were able to identify only four studies where biochemical recurrence-free survival (BCRFS) in BNS cohorts was compared with non-BNS cohort. [16],[29],[31],[34] Remaining data comes from prospective and retrospective single arm studies. Friedlander et al. assessed PSA, surgical margin status and pathological stage and grade and demonstrated no difference in BCRFS between BNS and control groups with a follow-up period of up to 72 months (hazard ratio 1.20, 95% confidence interval 0.62-2.31, P = 0.596). Similarly, in their prospective, controlled study, Bianco et al. reported that during 7-year of follow-up, BNS did not compromise disease free survival (DFS). Univariable and multivariable analyses of PSM at BNS was not a statistically important factor for DFS. Licht et al. also assessed DFS between BNS and non-BNS groups and showed no statistical difference. Gaker et al. reported that at 5.2-year follow-up, 90% of BNS group had a PSA of less than 0.2 mcg/L and 80% of the non-BNS group had a PSA of less than 0.2 mcg/L at 12.5-year of follow-up.

Functional outcomes

Urinary continence


Post-operative return to UC is similar in the reported ORP, LRP and RALP series. Where the BN was preserved UC varies between 36% and 100% at 1 month and 84% to 100% at 12 months follow-up. [Table 2] summarises the relevant studies. As with the assessment of oncological outcomes, only one study provides 1b level of evidence. The remaining studies constitute level of evidence 2-4. The method of assessment of UC post-RP has always been controversial and there is no consensus definition. [38] In a prospective study Lowe defined UC as usage of zero pads per day. In his series, UC at 1 month was 23% in the BNS group and 11% in the non-BNS group were continent, which was statistically significant. [39] Long-term UC was similar, 89% and 86% BNS and non-BNS cohorts respectively. Shelfo et al. reported a similar rate of post-operative UC of 88% at 6 months. [28] Connolly et al. studied continence in patients undergoing ORP and bladder BNr (anterior bladder tube reconstruction [ABTR] vs. tennis racket repair [TRR]). [40] Pre-and post-operative urodynamics studies were performed to evaluated continence parameters. All patients were continent post-operatively at 3 months. Differences in maximal urethral closing pressures were the only statistically significant findings between both groups post-operatively. Following analysis, preservation of functional urethral length was significantly longer in patients undergoing ABTR. The authors concluded that preservation of urethral length may promote UC post-ORP. Furthermore, Poon et al. compared outcomes of BNS with ABTR and TRR. [2] At intervals of 1 week, 4 weeks, 3 months, 6 months and 12 months there was no statistical difference in UC among those groups. No significant difference in UC at 6 months was noted by Srougi et al., however, due to the high prevalence of PSM at the BN recruitment to the study was halted pre-maturely. [3] A significant improvement in UC post-BNS was reported by Gaker and Steel, and Deliveliotis et al.[16],[41] In both prospective studies, early return of UC in BNS groups was noted compared to control groups, which was statistically important. In 2004 Selli et al. reported similar results from their series. [42] The study of 600 patients undergoing LRP reported a return to UC at 12 months at 84%. [43] Similar results were reported by Bordeaux [10] Leipzig [44] and Warsaw [45] groups. In our institution, we performed a retrospective analysis of 559 LRP. BNS was associated with a statistically insignificant faster recovery of UC at 3 months and statistically significant difference in UC at 12 months between BNS and non-BNS groups, 94.9% and 80.1%, respectively using one pad or less as a definition of continence. More recently, studies aiming at evaluation of BNS technique in RALP have been published. Freire et al. reported significantly better early UC in BNS group versus non-BNS group at 65.6% and 26.5% respectively. [30] At 2-year follow-up, there was no statistical difference between BNS and non-BNS groups and was 100% and 96.1%, respectively. In 2012 Friedlander et al., in a large retrospective cohort of 1067 men showed a significant improvement in early UC between BNS and control groups particularly at 5 and 12 months follow-up. [31] In another study, You et al. compared functional outcomes of RALP with BNS and BNS plus posterior urethral reconstruction (PUR); [46] however, their study was performed retrospectively on a relatively small sample. Nevertheless, it demonstrated a significant improvement in return to UC between a control and PUR groups and control and BNS-PUR groups. There was no significant advantage of BNS plus PUR technique over PUR alone. The authors concluded that PUR and BNS are related with improved UC post-RALP. The only prospective, randomised, controlled, blinded study comes from the Heidelberg group. [18] They demonstrated a significant early return of UC at 4 months follow-up. 84.2% of patients with BNS were continent compared with 55.3% in non-BNS procedure. Similarly at 12 months, the difference in UC was statistically significant and rates were 94.5% and 81.4% for BNS and non-BNS groups. Moreover, in the multiple logistic regression analysis BNS was an independent positive predictor of UC.
Table 2: Functional outcomes post-BNS

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Anastomotic strictures

Gomez et al. were reported that neo vesico-urethral anastomosis stricture rate were lower in BNS group compared with the non-BNS group. [23] Licht et al. confirmed a similar association. [34] Subsequent literature consistently supported these findings and currently there is an agreement that stricture rate post-BNS is relatively lower than in patients not undergoing BNS. Shelfo et al quoted 1% stricture rate in their study. [28] Poon et al. reported BN stricture at 5% for BNS and 11-18% for BNr techniques. [2] Gaker and Steel in 2004 reported that 2.9% of BNS patient had an anastomotic stricture. [16] Other studies present similar findings. [26],[41],[47] In 2004, Besarani et al. demonstrated that strictures occur mostly within 3 months post-surgery (75%) and are less frequent after 12 months from surgery (5%). [48] Freire et al. reported 1.1% anastomotic strictures in BNS compared with 0.7% in a control group. [30] More recently, the Heidelberg group did not observe the occurrence of any BN strictures post-RP in either BNS and control groups. [18]

Available evidence suggests that BNS technique is likely to be superior to non-BNS for preventing anastomotic strictures. However, most of evidence comes from non-randomised trials hence level of evidence is relatively low.


   Discussion Top


There is a growing body of literature on the role of BNS in RP, although outcome data is still mainly based on non-randomised, prospective and retrospective studies with variable sample size (level 2-4 evidence). Only one randomised, controlled, blinded study has been performed to date (level 1b). In the studies reviewed, PSM rates varied between 6% and 32%. Two series reported on the negative impact of BNS on the PSM. Katz et al. in his prospective series reported that after abandoning the BNS technique the PSM rate dropped by 9.75%, however, total PSM rate was still 26%. [32] Those findings were not confirmed by other studies, which documented that PSM did not negatively correlate with BNS technique. Moreover, newer, larger review postulates that sole PSM at BN is very rare (1.2%) and if present confers 12-year cancer free survival of 92%. [37] Some studies discussed the issue of indications and contra-indications for BNP technique. [12],[28],[33],[34],[35] While there is no agreement, it appears that the only absolute contraindication is high risk disease which increases the risk of PSM involving BN. A relative contraindication is a previous pelvic or transurethral prostate surgery as this may increase technical intraoperative difficulties. Some authors postulate additional investigations pre-operatively such as additional bladder base biopsies, pre-operative magnetic resonance imaging, and biopsies of the spared BN. The only randomised, prospective study on the subject concluded that BNS does not negatively impact oncological outcomes. [18] The sole PSM rate at BN was only 2% compared with total PSM rate being 13.6%.

This study also reported objective and subjective assessment of UC and demonstrated that BNS enables early return of UC and long-term UC. In the remaining studies included in our review, varying definitions of UC were used and therefore comparative analysis is not feasible. Two studies in the current review don't contain information on continence definition applied. [45],[47]

Lowe et al. defined UC as zero pads per day [39] while Srougi et al.'s definition was 1 pad/day. [3] Other series used an open interview as a method of assessment of UC without any validated questionnaires. More recently International Continence Society (ICS) male and ICS male short-form were utilised by others. Available data uniformly shows that UC rates post-RP with BNS are at least as good as post non-BNS and it is very likely that BNS expedites early return of UC and improves long-term UC.


   Conclusion Top


With changes in surgical technique, BNS has been increasingly incorporated into the RP. Evidence summarised in this review demonstrates that BNS technique leads to early return of UC and long-term UC without compromising oncological outcomes. Anastomotic stricture rate is lower when using BNS technique. BNS is superior to non-BNS techniques and authors of this review postulate application of the method in feasible cases. High risk prostate cancer cases must be considered separately.

 
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    Tables

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    Abstract
   Introduction
   Discussion
   Conclusion
    References
    Article Tables

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