Skip to main content
  • Research article
  • Open access
  • Published:

Clinical outcome of laparoscopic versus robot-assisted radical cystectomy for patients with bladder cancer: a retrospective study

Abstract

Background

With the development of minimally invasive surgery technology, patients with bladder cancer are increasingly receiving laparoscopic radical cystectomy (LRC) or robotic-assisted radical cystectomy (RARC) treatment. The main purpose of this study was to compare the long-term outcomes of bladder cancer patients treated with LRC versus RARC.

Methods

A retrospective study to identify patients with clinical stage Ta/T1/Tis to T3 bladder cancer who underwent RARC or LRC has been performed. The perioperative outcome, recurrence, and overall survival (OS) of the two surgical methods were compared.

Results

218 patients were identified from March 2010 to December 2019 in our department, which including 82 (38%) patients who received LRC and 136 (62%) patients who received RARC. There was no significant difference between the two groups in terms of lymph node collection, lymph node positive rate, resection margin positive rate, and postoperative pathological staging. Compared with the LRC group, patients in the RARC group had a median estimated blood loss (180 vs. 250 ml; P = 0.02) and reduced complications at 90 days postoperatively (30.8% vs. 46.3%; P = 0.01). Recurrence, all-cause death, and cancer-specific death occurred in 77 (35%), 55 (25%), and 39 (18%) patients, respectively. The 5-year OS rate was 54.63% and 54.65% in the RARC and LRC group (P > 0.05). The 5-year cancer-specific survival (CSS) rate was 73.32% and 61.55% in RARC and LRC group (P > 0.05). There was no significant difference in OS [hazard ratio (HR) 1.083, 95% confidence interval (CI) 0.626–1.874; P = 0.78], and CSS (HR 0.789, 95%CI 0.411–1.515; P = 0.61) between two groups.

Conclusions

Both RARC and LRC were safe and effective with a similar long-term clinical outcomes. Moreover, RARC had significantly lower median estimated blood loss and reduced postoperative complications.

Peer Review reports

Background

Bladder cancer is the most common urinary system malignant tumor in China. According to the 2018 Global Cancer Statistics Report, bladder cancer has already become 8th in the rank of tumors. Approximately, 20–30% of patients have muscular invasive bladder cancer (MIBC). For patients with MIBC, radical cystectomy plus pelvic lymph node dissection is the standard of care. Open radical cystectomy is still the most common used approach of cystectomy in clinical practice. However, the complication of surgical procedure has a high perioperative complication rate and significant mortality [1,2,3]. In the past decades, the development of laparoscopic instruments and technology became mature, making laparoscopic as a new treatment option for patients with bladder cancer. At the same time, many advantages of the Da Vinci robot system has already showing up. Our department has carried out complete laparoscopic radical cystectomy plus orthotopic ileal neobladder since 2010, and robot-assisted radical cystectomy plus orthotopic ileal neobladder since 2014. Considering only few evidence on the comparison of the long-term clinical outcomes between patients treated with laparoscopic radical cystectomy (LRC) or robot-assisted radical cystectomy (RARC), this study aimed to investigate the perioperative and long-term outcomes of bladder cancer patients treated with LRC versus RARC.

Materials and methods

Patients’ screening

A retrospective study aimed to determine the clinical stage of Ta/T1/Tis to T3 bladder cancer patients receiving RARC or LRC. All patients received routine serum testing, abdominal or pelvic volume computed tomography (CT), and cardiopulmonary function testing. The individual patient’s disease characteristics and comorbidities, even the patient’s financial status, surgeon’s and patient’s preferences are recorded. This study was approved by the Ethics Committee of Zhejiang Provincial People's Hospital.

Surgical process

All patients underwent general anesthesia. Operations were performed by three experienced surgeons for both laparoscopic and robotic-assisted operation. Both groups underwent radical cystectomy and systematic bilateral pelvic lymph node dissection with orthotopic ileal neobladder, and the urinary diversion was performed intracorporeally. The steps of surgical procedures were performed as previously reported [4, 5].

Patients’ characteristics and outcomes

Patients’ characteristics including age, gender, body mass index (BMI), American Society of Anesthesiologists (ASA) score, previous medical history (smoking history, hypertension, diabetes, cardiac disease, and operation history), and preoperative neoadjuvant chemo-therapy were recorded. Perioperative outcomes including type of urinary diversion, operative time, estimated blood loss, rate of intraoperative trans-fusion and postoperative hospital stay were compared between two groups. The intra-operative and postoperative complications were classified according to the modified Clavien–Dindo classification system. Pathologic outcomes including total number of lymph nodes removed, surgical margin, and pathologic stage were also recorded and compared. The identification of cancerous cells at the level of the inked parenchymal excision surface was regarded as a positive surgical margin. All patients were tested with physical examinations, laboratory tests, chest radiography, and abdominal and pelvic ultrasonography or computed tomography during follow-up period. The follow-up arrangement was every 3 months for the initial 2 years, every 6 months for the next 2 years, and annually thereafter. Long-term outcomes including disease-free survival (DFS), overall survival (OS), and cancer-specific survival (CSS) were collected.

Statistical analysis

Our research and data analysis follow the STROBE guidelines. Classification data is collected and analyzed as numbers and percentages. Standard deviation (SD) is used to check aggregated continuous data. Use the Chi-square test for categorical data and the Student’s t test or the Mann–Whitney U test for continuous variables to explore the difference between the LRC and RARC groups. OS is calculated from the day of surgery to the time of any cause-related death or the last follow-up. DFS is calculated from the day of surgery to the date of cancer recurrence or death from any cause. CSS is calculated from the date of diagnosis to the date of death due to bladder cancer. A Kaplan–Meier curve with a two-sided log-rank test and a Cox proportional hazard model with a calculated hazard ratio (HR) and 95% confidence interval (CI) were used to determine survival differences. All P values are two-sided and are considered significant when P < 0.05. All statistical analyses were performed using SPSS statistical software version 22.0 (SPSS Inc., Chicago, IL, USA).

Results

Patients’ population

218 patients were identified, including 82 (38%) received LRC and 136 (62%) received RARC. The median age and body mass index were 62 years old and 24.5 kg/m2. The majority of patients were male (76.1%), and the ASA score was low (1–2 points; 83.9%). Patient characteristics are summarized in Table 1. The distribution of age, sex, smoking history, BMI, American Society of Anesthesiologists (ASA) score, operation history, chronic disease was comparable between two groups. Only one patient (1.2%) in the LRC group and two patients (1.4%) in the RARC group had received neoadjuvant chemotherapy. The age, proportion of male patients, BMI, ASA score classification, past medical history, and neoadjuvant chemotherapy rate were also similar in the two groups.

Table 1 Patients characteristics

Perioperative outcomes

The operative time of RARC group was slightly longer than that of the LRC group, but the difference was not statistically significant. The median intraoperative estimated blood loss was 200 (range 100–480) mL and blood transfusion was performed in 24 (11%) patients. Patients received RARC had a significant less median estimated blood loss (250 vs. 180 mL; P = 0.02). The median hospitalization was 15 (13–22) days, and the intraoperative complication rate was presented in 11 (5%) patients. Intraoperative blood loss was higher in the LRC group than in the RARC group, but there was no difference in blood transfusion rate between two groups. The exhaust time was 2 (1–3) days, the feeding time of solid food was 4 (3–5) days, the total complication rate within 30 days was 28.0%, and the complication occurrence rate within 90 days was 37.2%. All patients were removed catheters and bilateral single J tubes after 13–15 days post-operation. There were no significant differences between the RARC and LRC group in terms of postoperative exhaust and feeding time, postoperative hospital stays, and the incidence of complications within 30 days after surgery. Of note, the incidence of complications and grade I–II complications within 90 days after surgery was dramatically lower in the RARC group than those in the LRC group (30.8% vs. 46.3%; P = 0.01), but there was no difference in grade III–IV complications (Table 2).

Table 2 Surgical outcomes and perioperative complications

Pathologic outcomes

Pathologic outcomes for LRC and RARC were shown in Table 3. Positive nodes were identified in 9.6% and positive surgical margin was identified in 2.7% of all included patients. Lymph node yields with median node counts of 19 for LRC and 20 for RARC (P = 0.18). Postoperative tumor pathological stages revealed that 48 cases in Ta/T1/Tis stage, 134 cases in T2 stage, and 36 cases in T3 stage. There was no statistical difference in the number of lymph node dissection, positive lymph node rate, positive rate of resection margin and postoperative pathological stage between two groups.

Table 3 Pathological outcomes

Long-term outcomes

The median follow-up was 33.0 months (IQR, 20.6–48.2 month). The recurrence, all-cause death, and cancer-specific death occurred in 77 (35%), 55 (25%), and 39 (18%) patients, respectively. The 5-year DFS was 55.07% in the RARC group and 48.18% in the LRC group. The 5-year OS rate was 54.63% in the RARC group and 54.65% in the LRC group (P > 0.05). The 5-year cancer-specific survival (CSS) rate was 73.32% in the RARC group and 61.55% in LRC group (P > 0.05). Importantly, there was no significant difference in OS (HR 1.083, 95%CI 0.626–1.874; P = 0.78) and CSS (HR 0.789, 95%CI 0.411–1.515; P = 0.61) between two groups (Figs. 1, 2, 3). There was 21 patients has been lost during the long-term outcomes.

Fig. 1
figure 1

Kaplan–Meier curves of overall survival comparison in patients treated with RARC versus LRC. 5-years-OS = (RARC: 54.63%, LRC: 56.648%); P = 0.7757; HR = 1.083; 95CI = (0.6259 to 1.874)

Fig. 2
figure 2

Kaplan–Meier curves of disease-free survival comparison in patients treated with RARC versus LRC. 5-years-PFS = (RARC: 55.066%, LRC: 48.175%); P = 0.6426; HR = 0.8297; 95CI = (0.5205 to 1.323)

Fig. 3
figure 3

Kaplan–Meier curves of cancer-specific survival comparison in patients treated with RARC versus LRC. 5-years-CSS = (RARC: 73.318%, LRC: 61.554%); P = 0.6143; HR = 0.7891; 95CI = (0.4112 to 1.515)

Discussion

Radical cystectomy was considered as standard-of-care for patients with MIBC [6]. Since 1990s, open radical cystectomy was the only surgical approach for the treatment of MIBC or high-risk non-MIBC. However, perioperative complication rate and mortality rate remained high and unsatisfactory due to the complicated surgical procedure. With the rapid development of minimally invasive techniques, LRC and RARC have become more and more important for the treatment of invasive bladder cancer [6] and have been extensively performed in many medical centers. The advantages of LRC and RARC included reduced complication rate and quick recovery post-operation [7,8,9,10], and the safety and efficacy of LRC and RARC are analogous to open radical cystectomy [11, 12]. Our department completed the first case of LRC and orthotopic neobladder reconstruction since 2010. Then, we gradually improved the details of the surgical procedure and began to perform RARC and orthotopic neobladder reconstruction since 2014. In clinical practice, we found patients received RARC had few blood loss and postoperative complications. To further compare the perioperative and long-term outcomes of these two surgical approaches in bladder cancer patients, we conducted this study to summarize the characteristics of the perioperative period and results of bladder cancer patients treated with LRC or RARC.

Although the RARC group reveals longer operation time comparted to LRC, it did not reach the statistical difference. Intraoperative blood loss was significantly higher in the LRC group then in the RARC group. Intraoperative blood transfusion rate and intraoperative complication rate were similar between two groups. In general, the difference between LRC and RARC might due to the inside and outside of the learning curve, surgeon’s experience, and the reasons for the renewal of surgical equipment. The difference in intraoperative blood loss seems related to different hemostatic methods and robotic instruments. The robotic surgery system has the characteristics of stable mechanical arm and lack of dead angle in the cavity. Whether it is separated or on the hemostatic clip, it could choose the best angle to cut into the desired level. In the narrow space condition, it would be better than laparoscopic surgery, and the high-definition three-dimensional vision system of the robot system could provide better anatomical structure and the direction of blood vessels to avoid damages [13,14,15]. Notably, the intraoperative, and postoperative complication rates were similar between two groups which were consistent with previous reports [16, 17]. There was also no difference on the intraoperative complication rate and the 30-day postoperative complication rate between two groups. However, patients in RARC group had markedly reduced 90-days postoperative complications than those in LRC group. Then we analyzed detailed data of 90-days post-operative complications. Most of the complications were urinary tract infection, pyelonephritis, lymphatic cysts, mild hydronephrosis, and small bladder stones. Most of them improved after conservative treatment or outpatient treatment. Additionally, we found that the potential reason for different complication rates between the two groups might be the improvement of the bladder suture methods. The RARC was mostly completed in the later period of the study. Several new methods including the U-shaped method could reduce the length of the intestine and maximize the length of the bladder, thus resulted in releasing the anastomotic tension between new bladder and urethra. The incidence of urinary fistula or obstruction would decrease. According to the previous experience, the new bladder is usually taken 30–35 cm ileum in the later period. The length-to-width ratio of the new bladder is about 4:3. During 3 months post-operation, the bladder volume will gradually expand after repeated expansion, then the bladder would be transforming to a new bladder with suitable volume and low pressure. Since the new bladder has relatively enough volume to keep the urine, it could reduce the urinary tract infection and protect renal function.

The reasons why patients received these operations had satisfactory outcomes and less complications may include: (i) the enlarged field of view under the endoscopic could provide satisfactorily view of neurovascular bundle and the urethra, which could reduce the damage of the ureter, keep better blood supply, and preserve appropriate ureteral length; (ii) the RARC could perform better quality anastomosed among urethra, ureter and new bladder. Complete operation inside the human body could minimize the anastomotic tension and prevent the twisting of the ureter or intestine; (iii) the single J tube inserted during the operation caused the new bladder under low pressure, which could prevent urinary leakage, reduce the probability of infection, ureteral stricture and reflux; (iv) we performed the new bladder with endovascular gastrointestinal anastomosis stapler, which could provide cutting and anastomosis been completed at same time; (v) the operation was completely performed in the abdominal cavity, avoiding the exposure of abdominal organs in the air which reducing the invisible water loss during the operation, the post-operation fasting time was shorter than before and the digestive function recovers quickly.

The postoperative pathology were mostly ≤ T2 stage (87.5%). The positive rates of lymph nodes were 9.8% and 8.8% in LRC and RARC, respectively. The positive rate of surgical margin was 2.4% and 2.9% in LRC and RARC, respectively. Compared with previous studies, the overall pathological results showed lower positive rates of lymph nodes and positive surgical margins [18, 19]. These differences might due to patients included in this study were all treated with orthotopic neobladder reconstruction. Thus mostly patients diagnosed with lower pathological stage before surgery. LRC and RARC found no difference in pathological T stage, positive lymph nodes or positive surgical margins, which is consistent with previous publication [20].

Although these results had several therapeutic implications, several limitations should be mentioned in this study. First, the sample size was small and the retrospective feature of this study will inevitably have selection bias. Thus, the results should be interpreted with caution and large-scale study especially a prospective one is still needed. Second, although the three surgeons are all experienced in endoscopic surgery, there were many other objective factors could influence the surgical outcomes [21,22,23,24]. RARC may get benefit from the late joined of the study which could affect the comparison results. Third, we did not record the functional data on daytime and nighttime continence. Last but not least, relatively shorter follow-up period may also become one of the limitations. Therefore, whether cystectomy under minimally invasive techniques and ileal orthotopic cystectomy can replace open surgery still remain undetermined [25,26,27]. Long-term, multicenter studies or randomized trials are still needed in the future.

Conclusion

In summary, both LRC and RARC are safe and effective with a similar long-term clinical outcomes to treat muscular invasive or high-risk non-muscular invasive bladder cancers. And more, RARC has better performance than LRC in reducing intraoperative bleeding and postoperative complications. RARC had significantly lower median estimated blood loss and reduced postoperative complications. Whether RARC could replace LRC as a new standard surgical method for patients with bladder cancer need future investigation.

Availability of data and materials

The datasets analysed during the current study are available from the corresponding author on reasonable request.

Abbreviations

LRC:

Laparoscopic radical cystectomy

RARC:

Robot-assisted radical cystectomy

OS:

Overall survival

CSS:

Cancer-specific survival

DFS:

Disease-free survival

HR:

Hazard ratio

95%CI:

95% Confidence interval

BMI:

Body mass index

ASA:

American Society of Anesthesiologists score

References

  1. Peyronnet B, et al. Oncological outcomes of laparoscopic nephroureterectomy versus open radical nephroureterectomy for upper tract urothelial carcinoma: an European Association of Urology guidelines systematic review. Eur Urol Focus. 2017;17(2):e1723–4.

    Article  Google Scholar 

  2. Piszczek R, Nowak Ł, Krajewski W, et al. Oncological outcomes of laparoscopic versus open nephroureterectomy for the treatment of upper tract urothelial carcinoma: an updated meta-analysis. World J Surg Oncol. 2021;19(1):129.

    Article  Google Scholar 

  3. Alothman KI, Mehmood S, Alzahrani HM, et al. Surgical and oncological outcome after laparoscopic versus open nephroureterectomy for non-metastatic, upper-tract urothelial carcinoma. A single-centre experience. Saudi Med J. 2020;41(1):25–33.

    Article  Google Scholar 

  4. Simone G, Papalia R, Misuraca L, et al. Robotic intracorporeal padua ileal bladder: surgical technique, perioperative, oncologic and functional outcomes. Eur Urol. 2018;73(6):934–40.

    Article  Google Scholar 

  5. Beecken WD, Wolfram M, Engl T, et al. Robotic-assisted laparoscoplc radical cystectomy and intra-abdominal formation of an orthotopic ileal neobladder. Eur Urol. 2003;44:337–9.

    Article  Google Scholar 

  6. Alfred Witjes J, Lebret T, Compérat EM, et al. Updated 2016 EAU guidelines on muscle-invasive and metastatic bladder cancer. Eur Urol. 2017;71(3):462–75.

    Article  CAS  Google Scholar 

  7. Resicce F, Leonardo C, Tuderti G, et al. Late complications of robot-assisted radical cystectomy with totally intracorporeal urinary diversion. World J Urol 2020(3)

  8. Johar RS, Hayn MH, Stegemann AP, et al. Complications after robot- assisted radical cystectomy: results from the International Robotic Cystectomy Consortium. Eur Urol. 2013;64:52–7.

    Article  Google Scholar 

  9. Peng L, Li J, Cao D, et al. Can robotic-assisted radical cystectomy provide patients with a smaller trauma and faster recovery period? A systematic review and meta-analysis of comparative trials. J Cancer Res Clinl Oncol. 2020;146(6):1591–601.

    Article  Google Scholar 

  10. Ishii H, Rai BP, Stolzenburg JU, et al. Robotic or open radical cystectomy, which is safer? A systematic review and meta-analysis of comparative studies. J Endourol. 2014;28(10):1215–23.

    Article  Google Scholar 

  11. Aboumarzouk OM, Hughes O, Narahari K, Drewa T, Chlosta PL, Kynaston H. Safety and feasibility of laparoscopic radical cystectomy for the treatment of bladder cancer. J Endourol. 2013;27:1083–95.

    Article  Google Scholar 

  12. Tang K, Li H, Xia D, et al. Laparoscopic versus open radical cystectomy in bladder cancer: a systematic review and meta-analysis of comparative studies. PLoS ONE. 2014;9:e95667.

    Article  Google Scholar 

  13. Kanno T, et al. Oncological outcomes and recurrence patterns after laparoscopic radical cystectomy for bladder cancer: a Japanese multicenter cohort. Int J Urol. 2020;27(3):250–6.

    Article  Google Scholar 

  14. Su S, et al. Comparison of laparoscopic and robot-assisted radical cystectomy for bladder cancer: perioperative and oncologic outcomes. Clin Genitourin Cancer. 2019;17(5):e1048–53.

    Article  Google Scholar 

  15. Teishima J, Hieda K, Inoue S, et al. Comparison of initial experiences of robot-assisted radical cystectomy with those of laparoscopic for bladder cancer. Innovations (Phila). 2014;9:322–6.

    Article  Google Scholar 

  16. Kubota Y, Nakaigawa N. Essential content of evidence-based clinical practice guidelines for bladder cancer: the Japanese Urological Association 2015 update. Int J Urol. 2016;23:640–5.

    Article  Google Scholar 

  17. Satkunasivam R, et al. Robot-assisted radical cystectomy versus open radical cystectomy: a meta-analysis of oncologic, perioperative, and complication-related outcomes. Eur Urol Oncol. 2019;2(4):443–7.

    Article  Google Scholar 

  18. Milenkovic U, Akand M, Moris L, et al. Impact of neoadjuvant chemotherapy on short-term complications and survival following radical cystectomy. World J Urol. 2019;37:1857–66.

    Article  CAS  Google Scholar 

  19. Rai BP, Bondad J, Vasdev N, et al. Robotic versus open radical cystectomy for bladder cancer in adults. Cochrane Database Syst Rev. 2019;4(4):CD011903.

    PubMed  Google Scholar 

  20. Parekh DJ, Reis IM, Castle EP, et al. Robot-assisted radical cystectomy versus open radical cystectomy in patients with bladder cancer (RAZOR): an open-label, randomised, phase 3, non-inferiority trial. Lancet. 2018;391(10139):2525–36.

    Article  Google Scholar 

  21. Novara G, Catto JW, Wilson T, et al. Systematic review and cumulative analysis of perioperative outcomes and complications after robot-assisted radical cystectomy. Eur Urol. 2015;67(3):376–401.

    Article  Google Scholar 

  22. Yuh B, Wilson T, Bochner B, et al. Systematic review and cumulative analysis of oncologic and functional outcomes after robot-assisted radical cystectomy. Eur Urol. 2015;67(3):402–22.

    Article  Google Scholar 

  23. Chan KG, Guru K, Wiklund P, et al. Robot-assisted radical cystectomy and urinary diversion: technical recommendations from the Pasadena Consensus Panel. Eur Urol. 2015;67(3):423–31.

    Article  Google Scholar 

  24. Wilson TG, Guru K, Rosen RC, et al. Best practices in robot-assisted radical cystectomy and urinary reconstruction: recommendations of the Pasadena Consensus Panel. Eur Urol. 2015;67(3):363–75.

    Article  Google Scholar 

  25. Briganti A, et al. Surgical safety of radical cystectomy and pelvic lymph node dissection following neoadjuvant pembrolizumab in patients with bladder cancer: prospective assessment of perioperative outcomes from the PURE-01 Trial. Eur Urol. 2020;77(5):576–80.

    Article  CAS  Google Scholar 

  26. Bochner BH, Dalbagni G, Sjoberg DD, et al. Comparing open radical cystectomy and robot-assisted laparoscopic radical cystectomy: a randomized clinical trial. Eur Urol. 2015;67:1042–50.

    Article  Google Scholar 

  27. Goh AC, Gill IS, Lee DJ, et al. Robotic intracorporeal orthotopic ileal neobladder: replicating open surgical principles. Eur Urol. 2012;62(5):891–901.

    Article  Google Scholar 

Download references

Acknowledgements

We would like to thank the Department of Urology, Zhejiang Provincial People’s Hospital for the population and optimization of laparoscopic techniques in order to benefit patients. In addition, we would like to thank all the patients for giving us the permission to use the medical information for this publication.

Funding

Open access funding provided by the Zhejiang Clinical Research Center of Minimally Invasive Diagnosis and Treatment of Abdominal Diseases (No. 2018E50003) and Key research projects of traditional Chinese medicine in Zhejiang Province (No.2017ZZ002).The source of funding had no role in the design of the study and collection, analysis, and interpretation of data and in writing the manuscript.

Author information

Authors and Affiliations

Authors

Contributions

DHZ and SW, XLQ: Project development. YCB, EH Li and JQ: Manuscript writing. WZ, QZ and FW: Data collection and analysis. All authors read and approved the final manuscript.

Corresponding author

Correspondence to DaHong Zhang.

Ethics declarations

Ethics approval and consent to participate

All study participants were informed about the planned procedure and signed informed consent. The study was approved by the ethics committee of Zhejiang Provincial People's Hospital, HangZhou city, China.

Consent for publication

Not applicable.

Competing interests

The authors declared that they have no competing interests.

Additional information

Publisher's Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

Bai, Y., Wang, S., Zheng, W. et al. Clinical outcome of laparoscopic versus robot-assisted radical cystectomy for patients with bladder cancer: a retrospective study. BMC Surg 21, 388 (2021). https://doi.org/10.1186/s12893-021-01382-1

Download citation

  • Received:

  • Accepted:

  • Published:

  • DOI: https://doi.org/10.1186/s12893-021-01382-1

Keywords