Abstract
Purpose
To describe and compare differences in peri-operative outcomes of robot-assisted (RA-RPLND) and open (O-RPLND) retroperitoneal lymph node dissection performed by a single surgeon where chemotherapy is the standard initial treatment for Stage 2 or greater non-seminomatous germ cell tumour.
Methods
Review of a prospective database of all RA-RPLNDs (28 patients) and O-RPLNDs (72 patients) performed by a single surgeon from 2014 to 2020. Peri-operative outcomes were compared for patients having RA-RPLND to all O-RPLNDs and a matched cohort of patients having O-RPLND (20 patients). Further comparison was performed between all patients in the RA-RPLND group (21 patients) and matched O-RPLND group (18 patients) who had previous chemotherapy. RA-RPLND was performed for patients suitable for a unilateral template dissection. O-RPLND was performed prior to the introduction of RA-RPLND and for patients not suitable for RA-RPLND after its introduction.
Results
RA-RPLND showed improved peri-operative outcomes compared to the matched cohort of O-RPLND—median blood loss (50 versus 400 ml, p < 0.00001), operative duration (150 versus 195 min, p = 0.023) length-of-stay (1 versus 5 days, p < 0.00001) and anejaculation (0 versus 4, p = 0.0249). There was no statistical difference in complication rates. RA-RPLND had lower median lymph node yields although not significant (9 versus 13, p = 0.070). These improved peri-operative outcomes were also seen in the post-chemotherapy RA-RPLND versus O-RPLND analysis. There were no tumour recurrences seen in either group with median follow-up of 36 months and 60 months, respectively.
Conclusions
Post-chemotherapy RA-RPLND may have decreased blood loss, operative duration, hospital length-of-stay and anejaculation rates in selected cases and should, therefore, be considered in selected patients. Differences in oncological outcomes require longer term follow-up.
Similar content being viewed by others
Data availability
The data that support the findings of this study are available from the corresponding author upon reasonable request.
References
Motzer RJ, Agarwal N, Beard C, Bolger GB, Boston B, Carducci MA et al (2009) NCCN clinical practice guidelines in oncology: testicular cancer. J Natl Compr Canc Netw 7(6):672–693
Albers P, Albrecht W, Algaba F, Bokemeyer C, Cohn-Cedermark G, Fizazi K et al (2015) Guidelines on testicular cancer: 2015 update. Eur Urol 68(6):1054–1068
Chalfin HJ, Ludwig W, Pierorazio PM, Allaf ME (2016) Robotic primary RPLND for stage I testicular cancer: a review of indications and outcomes. Curr Urol Rep 17(5):41
Williams SB, McDermott DW, Winston D, Bahnson E, Berry AM, Steele GS et al (2010) Morbidity of open retroperitoneal lymph node dissection for testicular cancer: contemporary perioperative data. BJU Int 105(7):918–921
Rukstalis DB, Chodak GW (1992) Laparoscopic retroperitoneal lymph node dissection in a patient with stage 1 testicular carcinoma. J Urol 148(6):1907–1909 (discussion 9-10)
Steiner H, Leonhartsberger N, Stoehr B, Peschel R, Pichler R (2013) Postchemotherapy laparoscopic retroperitoneal lymph node dissection for low-volume, stage II, nonseminomatous germ cell tumor: first 100 patients. Eur Urol 63(6):1013–1017
Cheney SM, Andrews PE, Leibovich BC, Castle EP (2015) Robot-assisted retroperitoneal lymph node dissection: technique and initial case series of 18 patients. BJU Int 115(1):114–120
Pearce SM, Golan S, Gorin MA, Luckenbaugh AN, Williams SB, Ward JF et al (2017) Safety and early oncologic effectiveness of primary robotic retroperitoneal lymph node dissection for nonseminomatous germ cell testicular cancer. Eur Urol 71(3):476–482
Davol P, Sumfest J, Rukstalis D (2006) Robotic-assisted laparoscopic retroperitoneal lymph node dissection. Urology 67(1):199
Revenig L, Leung A, Hsiao W (2014) Ejaculatory physiology and pathophysiology: assessment and treatment in male infertility. Transl Androl Urol 3(1):41–49
Katz A, Dizon DS (2016) Sexuality after cancer: a model for male survivors. J Sex Med 13(1):70–78
Stepanian S, Patel M, Porter J (2016) Robot-assisted laparoscopic retroperitoneal lymph node dissection for testicular cancer: evolution of the technique. Eur Urol 70(4):661–667
Overs C, Beauval JB, Mourey L, Rischmann P, Soulie M, Roumiguie M et al (2018) Robot-assisted post-chemotherapy retroperitoneal lymph node dissection in germ cell tumor: is the single-docking with lateral approach relevant? World J Urol 36(4):655–661
Harris KT, Gorin MA, Ball MW, Pierorazio PM, Allaf ME (2015) A comparative analysis of robotic vs laparoscopic retroperitoneal lymph node dissection for testicular cancer. BJU Int 116(6):920–923
Mosharafa AA, Foster RS, Koch MO, Bihrle R, Donohue JP (2004) Complications of post-chemotherapy retroperitoneal lymph node dissection for testis cancer. J Urol 171(5):1839–1841
Cary C, Masterson TA, Bihrle R, Foster RS (2015) Contemporary trends in postchemotherapy retroperitoneal lymph node dissection: Additional procedures and perioperative complications. Urol Oncol 33(9):389.e15–21
Kamel MH, Littlejohn N, Cox M, Eltahawy EA, Davis R (2016) Post-chemotherapy robotic retroperitoneal lymph node dissection: institutional experience. J Endourol 30(5):510–519
Singh A, Chatterjee S, Bansal P, Bansal A, Rawal S (2017) Robot-assisted retroperitoneal lymph node dissection: feasibility and outcome in postchemotherapy residual mass in testicular cancer. Indian J Urol 33(4):304–309
Abdul-Muhsin HM, L’Esperance JO, Fischer K, Woods ME, Porter JR, Castle EP (2015) Robot-assisted retroperitoneal lymph node dissection in testicular cancer. J Surg Oncol 112(7):736–740
Darzi SA, Munz Y (2004) The impact of minimally invasive surgical techniques. Annu Rev Med 55:223–237
Tang K, Xia D, Li H, Guan W, Guo X, Hu Z et al (2014) Robotic vs. open radical cystectomy in bladder cancer: a systematic review and meta-analysis. Eur J Surg Oncol 40(11):1399–1411
Son SK, Lee NR, Kang SH, Lee SH (2017) Safety and effectiveness of robot-assisted versus open radical cystectomy for bladder cancer: a systematic review and meta-analysis. J Laparoendosc Adv Surg Tech A 27(11):1109–1120
Shen Z, Xie L, Xie W, Hu H, Chen T, Xing C et al (2016) The comparison of perioperative outcomes of robot-assisted and open partial nephrectomy: a systematic review and meta-analysis. World J Surg Oncol 14(1):220
Yaxley JW, Coughlin GD, Chambers SK, Occhipinti S, Samaratunga H, Zajdlewicz L et al (2016) Robot-assisted laparoscopic prostatectomy versus open radical retropubic prostatectomy: early outcomes from a randomised controlled phase 3 study. Lancet 388(10049):1057–1066
Li R, Duplisea JJ, Petros FG, Gonzalez GMN, Tu SM, Karam JA et al (2019) Robotic postchemotherapy retroperitoneal lymph node dissection for testicular cancer. Eur Urol Oncol. https://doi.org/10.1016/j.euo.2019.01.014
Stein JP, Penson DF, Cai J, Miranda G, Skinner EC, Dunn MA et al (2007) Radical cystectomy with extended lymphadenectomy: evaluating separate package versus en bloc submission for node positive bladder cancer. J Urol 177(3):876–881 (discussion 81)
Beck SD, Foster RS, Bihrle R, Donohue JP, Einhorn LH (2007) Is full bilateral retroperitoneal lymph node dissection always necessary for postchemotherapy residual tumor? Cancer 110(6):1235–1240
Carver BS, Shayegan B, Eggener S, Stasi J, Motzer RJ, Bosl GJ et al (2007) Incidence of metastatic nonseminomatous germ cell tumor outside the boundaries of a modified postchemotherapy retroperitoneal lymph node dissection. J Clin Oncol 25(28):4365–4369
Cho JS, Kaimakliotis HZ, Cary C, Masterson TA, Beck S, Foster R (2017) Modified retroperitoneal lymph node dissection for post-chemotherapy residual tumour: a long-term update. BJU Int 120(1):104–108
Heidenreich A, Pfister D, Witthuhn R, Thuer D, Albers P (2009) Postchemotherapy retroperitoneal lymph node dissection in advanced testicular cancer: radical or modified template resection. Eur Urol 55(1):217–224
Funding
No funds, grants, or other support were received.
Author information
Authors and Affiliations
Contributions
PL and BT participated in conception and design, statistical analysis, analysis and interpretation of data, and manuscript drafting. AH, EL, HD, JS, CA, SS, DM, HW, NL and AW collected the clinical data and analysis and interpretation of data. MF contributed to analysis and interpretation of data, and manuscript drafting. DN participated in project supervision. All the authors read and approved the final manuscript.
Corresponding author
Ethics declarations
Conflict of interest
Paul Lloyd, Anne Hong, Marc A. Furrer, Elaine WY Lee, Harveer S Dev, Maurice H Coret, James M Adshead, Peter Baldwin, Richard Knight, Jonathan Shamash, Constantine Alifrangis, Sara Stoneham, Danish Mazhar, Han Wong, Anne Warren, Ben Tran, Nathan Lawrentschuk, David E Neal and Benjamin C Thomas have nothing to disclose.
Ethical approval
Approval was obtained from the local ethics committee. Informed consent was waived by the institutional review board in view of the retrospective nature of the study. All the procedures being performed were part of the routine care.
Additional information
Publisher's Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Supplementary Information
Below is the link to the electronic supplementary material.
Rights and permissions
About this article
Cite this article
Lloyd, P., Hong, A., Furrer, M.A. et al. A comparative study of peri-operative outcomes for 100 consecutive post-chemotherapy and primary robot-assisted and open retroperitoneal lymph node dissections. World J Urol 40, 119–126 (2022). https://doi.org/10.1007/s00345-021-03832-0
Received:
Accepted:
Published:
Issue Date:
DOI: https://doi.org/10.1007/s00345-021-03832-0