Peritoneal interposition flap reduces symptomatic lymphocele following transperitoneal robot-assisted radical prostatectomy and pelvic lymph node dissection: An updated meta-analysis

João Henrique Sendrete de Pinho , Lorrane Vieira Siqueira Riscado , João Pádua Manzano

Current Urology ›› 2024, Vol. 18 ›› Issue (3) : 167 -176.

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Current Urology ›› 2024, Vol. 18 ›› Issue (3) :167 -176. DOI: 10.1097/CU9.0000000000000205
Advances in Prostate Cancer Research
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Peritoneal interposition flap reduces symptomatic lymphocele following transperitoneal robot-assisted radical prostatectomy and pelvic lymph node dissection: An updated meta-analysis
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Abstract

Background: Robot-assisted radical prostatectomy with intraoperative pelvic lymph node dissection is the criterion standard for surgical treatment of nonmetastatic intermediate- and high-risk prostate cancer. However, this method is associated with symptomatic lymphocele (SLC), which is an important morbidity factor. To overcome this complication, several modifications of the technique have been developed, including the peritoneal interposition flap (PIF). We performed an updated systematic review and meta-analysis to investigate the efficacy and safety of this technique for preventing SLC and lymphocele (LC) formation.

Materials and methods: Searches were performed using databases and references from included studies and previous systematic reviews. Only randomized controlled trials and nonrandomized cohorts were included. Primary outcomes were the incidence of SLC and LC formation, and safety outcomes were defined as operation time, estimated blood loss, length of hospital stay, and urinary incontinence. Quality assessment was performed using the Newcastle-Ottawa Scale and Cochrane Collaboration's tool. Pooled treatment effects were estimated using odds ratios with 95% confidence intervals (CIs) for binary endpoints. Heterogeneity was examined using Cochran's Q test and I2 statistics; p values < 0.10 and I2 > 25% were considered significant for heterogeneity. We used Mantel-Haenszel fixed-effect models in the analyses with low heterogeneity. Otherwise, the DerSimonian and Laird random-effects model was used.

Results: The initial search yielded 510 results. After the removal of duplicate records and application of the exclusion criterion, 9 studies were fully reviewed for eligibility. Three randomized controlled trials and 5 retrospective cohorts met all the inclusion criteria, comprising 2261 patients, of whom 1073 (47.4%) underwent PIF. Six studies reported a significant reduction in SLC in the PIF group, and 3 of the 4 studies reported LC formation yielded significant results in preventing this complication. The incidence of SLC and LC formation in a follow-up of ≥3 months was significantly different between the PIF and no PIF group (odds ratio, 0.34 [95% CI, 0.16-0.74; p = 0.006] and 0.48 [95% CI, 0.31-0.74; p = 0.0008]), respectively. The safety outcomes did not differ significantly between the 2 groups.

Conclusions: These results suggest that PIF is an effective and safe technique for preventing LC and SLC in patients undergoing transperitoneal robot-assisted radical prostatectomy and pelvic lymph node dissection.

Keywords

Robot-assisted radical prostatectomy / Lymphocele / Peritoneal reapproximation / Peritoneal interpolated flap / Meta-analysis

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João Henrique Sendrete de Pinho, Lorrane Vieira Siqueira Riscado, João Pádua Manzano. Peritoneal interposition flap reduces symptomatic lymphocele following transperitoneal robot-assisted radical prostatectomy and pelvic lymph node dissection: An updated meta-analysis. Current Urology, 2024, 18(3): 167-176 DOI:10.1097/CU9.0000000000000205

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Acknowledgments

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Statement of ethics

The present systematic review and meta-analysis was performed in accordance with the recommendations of the Cochrane Collaboration and PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analysis) statement guidelines.

Conflict of interest statement

No conflict of interest has been declared by the authors.

Funding source

None.

Author contributions

JHSP: Research design, writing of the paper, performance of the research, data collection, analysis, and interpretation;

LVSR: Writing of the paper, performance of the research and data collection;

JPM: Writing of the paper, analysis and interpretation;

All authors: Critical revision of the article and final approval.

Data availability

The datasets generated during and/or analyzed during the current study are not publicly available, but are available from the corresponding author on reasonable request.

References

[1]

Liss MA, Lusch A, Morales B, et al. Robot-assisted radical prostatectomy: 5-year oncological and biochemical outcomes. J Urol 2012; 188(6):2205-2210.

[2]

Dell'Oglio P, Mottrie A, Mazzone E. Robot-assisted radical prostatectomy vs. open radical prostatectomy: Latest evidences on perioperative, functional and oncological outcomes. Curr Opin Urol 2020; 30(1):73-78.

[3]

Mottet N, van den Bergh RCN, Briers E, et al. EAU-EANM-ESTRO-ESUR-SIOG guidelines on prostate cancer—2020 update. Part 1: Screening, diagnosis, and local treatment with curative intent. Eur Urol 2021; 79(2):243-262.

[4]

Sanda MG, Cadeddu JA, Kirkby E, et al. Clinically localized prostate cancer: AUA/ASTRO/SUO guideline. Part II: Recommended approaches and details of specific care options. J Urol 2018; 199(4):990-997.

[5]

Solberg A, Angelsen A, Bergan U, Haugen OA, Viset T, Klepp O. Frequency of lymphoceles after open and laparoscopic pelvic lymph node dissection in patients with prostate cancer. Scand J Urol Nephrol 2003; 37(3):218-221.

[6]

Zorn KC, Katz MH, Bernstein A, et al. Pelvic lymphadenectomy during robot-assisted radical prostatectomy: Assessing nodal yield, perioperative outcomes, and complications. Urology 2009; 74(2):296-302.

[7]

Khoder WY, Trottmann M, Buchner A, et al. Risk factors for pelvic lymphoceles post-radical prostatectomy. Int J Urol 2011; 18(9):638-643.

[8]

Briganti A, Chun FKH, Salonia A, et al. Complications and other surgical outcomes associated with extended pelvic lymphadenectomy in men with localized prostate cancer. Eur Urol 2006; 50(5):1006-1013.

[9]

Musch M, Klevecka V, Roggenbuck U, Kroepfl D. Complications of pelvic lymphadenectomy in 1,380 patients undergoing radical retropubic prostatectomy between 1993 and 2006. J Urol 2008; 179(3):923-928; discussion 928-929.

[10]

Augustin H, Hammerer P, Graefen M, et al. Intraoperative and perioperative morbidity of contemporary radical retropubic prostatectomy in a consecutive series of 1243 patients: Results of a single center between 1999 and 2002. Eur Urol 2003; 43(2):113-118.

[11]

Keskin MS, Argun ÖB, Öbek C, et al. The incidence and sequela of lymphocele formation after robot-assisted extended pelvic lymph node dissection. BJU Int 2016; 118(1):127-131.

[12]

Lebeis C, Canes D, Sorcini A, Moinzadeh A. Novel technique prevents lymphoceles after transperitoneal robotic-assisted pelvic lymph node dissection: Peritoneal flap interposition. Urology 2015; 85(6):1505-1509.

[13]

Deutsch S, Hadaschik B, Lebentrau S, Ubrig B, Burger M, May M. Clinical importance of a peritoneal interposition flap to prevent symptomatic lymphoceles after robot-assisted radical prostatectomy and pelvic lymph node dissection: A systematic review and meta-analysis. Urol Int 2022; 106(1):28-34.

[14]

Moher D, Liberati A, Tetzlaff J, Altman DG; PRISMA Group. Preferred Reporting Items for Systematic Reviews and Meta-analyses: The PRISMA statement. PLoS Med 2009; 6(7):e1000097.

[15]

Wells G, Shea B, O'Connell D, et al. The Newcastle-Ottawa Scale (NOS) for assessing the quality of nonrandomised studies in meta-analyses. The Ottawa Hospital. 2021. Available at: https://www.ohri.ca//programs/clinical_epidemiology/oxford.asp. Accessed August 30, 2022.

[16]

Higgins JPT, Altman DG, Gøtzsche PC, et al. The Cochrane Collaboration's tool for assessing risk of bias in randomised trials. BMJ 2011;343:d5928.

[17]

Dal Moro F, Zattoni F. P.L.E.A.T.—Preventing lymphocele ensuring absorption transperitoneally: A robotic technique. Urology 2017;110:244-247.

[18]

Stolzenburg JU, Arthanareeswaran VKA, Dietel A, et al. Four-point peritoneal flap fixation in preventing lymphocele formation following radical prostatectomy. Eur Urol Oncol 2018; 1(5):443-448.

[19]

Bründl J, Lenart S, Stojanoski G, et al. Peritoneal flap in robot-assisted radical prostatectomy. Dtsch Arztebl Int 2020; 117(14):243-250.

[20]

Lee M, Lee Z, Eun DD. Utilization of a peritoneal interposition flap to prevent symptomatic lymphoceles after robotic radical prostatectomy and bilateral pelvic lymph node dissection. J Endourol 2020; 34(8):821-827.

[21]

Gloger S, Ubrig B, Boy A, et al. Bilateral peritoneal flaps reduce incidence and complications of lymphoceles after robotic radical prostatectomy with pelvic lymph node dissection—Results of the prospective randomized multicenter trial ProLy. J Urol 2022; 208(2):333-340.

[22]

Student V Jr., Tudos Z, Studentova Z, et al. Effect of peritoneal fixation (PerFix) on lymphocele formation in robot-assisted radical prostatectomy with pelvic lymphadenectomy: Results of a randomized prospective trial. Eur Urol 2023; 83(2):154-162.

[23]

Yılmaz K, Ölçücü MT, Arı Ö, et al. The results of peritoneal re-approximation methods on symptomatic lymphocele formation in robot-assisted laparoscopic radical prostatectomy and extended pelvic lymphadenectomy. Arch Esp Urol 2022; 75(5):447-452.

[24]

Waldert M, Remzi M, Klatte T, Klingler HC. FloSeal reduces the incidence of lymphoceles after lymphadenectomies in laparoscopic and robot-assisted extraperitoneal radical prostatectomy. J Endourol 2011; 25(6):969-973.

[25]

Buelens S, van Praet C, Poelaert F, van Huele A, Decaestecker K, Lumen N. Prospective randomized controlled trial exploring the effect of TachoSil on lymphocele formation after extended pelvic lymph node dissection in prostate cancer. Urology 2018;118:134-140.

[26]

Scholz HS, Petru E, Benedicic C, Haas J, Tamussino K, Winter R. Fibrin application for preventing lymphocysts after retroperitoneal lymphadenectomy in patients with gynecologic malignancies. Gynecol Oncol 2002; 84(1):43-46.

[27]

Kim WT, Ham WS, Koo KC, Choi YD. Efficacy of octreotide for management of lymphorrhea after pelvic lymph node dissection in radical prostatectomy. Urology 2010; 76(2):398-401.

[28]

Porpiglia F, Terrone C, Tarabuzzi R, et al. Transperitoneal versus extraperitoneal laparoscopic radical prostatectomy: Experience of a single center. Urology 2006; 68(2):376-380.

[29]

Chung JS, Kim WT, Ham WS, et al. Comparison of oncological results, functional outcomes, and complications for transperitoneal versus extraperitoneal robot-assisted radical prostatectomy: A single surgeon's experience. J Endourol 2011; 25(5):787-792.

[30]

Stolzenburg JU, Wasserscheid J, Rabenalt R, et al. Reduction in incidence of lymphocele following extraperitoneal radical prostatectomy and pelvic lymph node dissection by bilateral peritoneal fenestration. World J Urol 2008; 26(6):581-586.

[31]

Boğa MS, Sönmez MG, Karamık K, Yılmaz K, Savaş M, Ateş M. The effect of peritoneal re-approximation on lymphocele formation in transperitoneal robot-assisted radical prostatectomy and extended pelvic lymphadenectomy. Turk J Urol 2020; 46(6):460-467.

[32]

Magistro G, Tuong-Linh Le D, Westhofen T, et al. Occurrence of symptomatic lymphocele after open and robot-assisted radical prostatectomy. Cent European J Urol 2021; 74(3):341-347.

[33]

Goßler C, May M, Breyer J, et al. High BMI, aggressive tumours and long console time are independent predictive factors for symptomatic lymphocele formation after robot-assisted radical prostatectomy and pelvic lymph node dissection. Urol Int 2021; 105(5-6):453-459.

[34]

Gotto GT, Yunis LH, Guillonneau B, et al. Predictors of symptomatic lymphocele after radical prostatectomy and bilateral pelvic lymph node dissection. Int J Urol 2011; 18(4):291-296.

[35]

Tikkinen KAO, Cartwright R, Gould MK, et al. EAU guidelines on thromboprophylaxis in urological surgery. Eur Urol 2022. Available at: https://uroweb.org/guidelines/thromboprophylaxis/chapter/guideline. Accessed August 30, 2022.

[36]

Andrews JR, Sobol I, Frank I, et al. Treatment outcomes in patients with symptomatic lymphoceles following radical prostatectomy depend upon size and presence of infection. Urology 2020;143:181-185.

[37]

Luo D, Wan X, Liu J, Tong T. Optimally estimating the sample mean from the sample size, median, mid-range, and/or mid-quartile range. Stat Methods Med Res 2018; 27(6):1785-1805.

[38]

Shi J, Luo D, Weng H, et al. Optimally estimating the sample standard deviation from the five-number summary. Res Synth Methods 2020; 11(5):641-654.

[39]

Wan X, Wang W, Liu J, Tong T. Estimating the sample mean and standard deviation from the sample size, median, range and/or interquartile range. BMC Med Res Methodol 2014;14:135.

[40]

Neuberger M, Kowalewski KF, Simon V, et al. Peritoneal flap for lymphocele prophylaxis following robotic-assisted laparoscopic radical prostatectomy with pelvic lymph node dissection: Study protocol and trial update for the randomized controlled PELYCAN study. Trials 2021; 22(1):236.

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