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Intra-corporeal robot-assisted versus open radical cystectomy: a meta-analysis

In brief

Robot-assisted cystectomy reduces blood loss by 500 ml and hospital stay by two days

A meta-analysis of 30 studies (8857 patients) found that intra-corporeal robot-assisted radical cystectomy cut estimated blood loss by about 523 ml, lowered transfusion rates and shortened postoperative admission by roughly 2.3 days compared with open surgery, while modestly improving 5-year survival. The approach took longer to perform and was linked to more ureteroenteric strictures, and the survival advantage rests on mostly observational data, so high-quality trials are still needed.

Journal
World journal of urology (Q1)
Published
29 July 2026
Study design
Systematic review / meta-analysis of RCTs
Evidence level
Level 1, High (CEBM 1a)
Authors
Lijian Gan, Jiyue Wu, Zhen Li, Huawei Cao, Hao Wang, Yuqing Li, et al.
PMID
42525253
DOI
10.1007/s00345-026-06641-5

Why clinicians should know about it

  • Picked for Epidemiology (top studies of the week, 2 August 2026).
  • Picked for Urology (top studies of the week, 2 August 2026): Meta‑analysis shows robot‑assisted cystectomy superior to open surgery

Abstract

OBJECTIVE: To compare the safety and effectiveness between robot-assisted radical cystectomy with intracorporeal urinary diversion (iRARC) and open radical cystectomy (ORC). METHODS: We conducted this systematic review and meta-analysis of the primary outcomes of interest according to the PRISMA and AMSTAR Guidelines. Five databases were systematically searched, including Medline, PubMed, Cochrane Library, Scopus, and Web of Science. The search timeframe was set from database creation to February 2026. RESULTS: There were 30 studies including 8857 patients. Compared with ORC, iRARC was superior in terms of estimated blood loss [WMD=-523.18, 95% CI (-622.68, -423.68), P < 0.01], length of stay [WMD=-2.30, 95% CI (-3.27, -1.33), P < 0.01], lymph nodes removed [WMD = 2.39, 95% CI (0.16, 4.62), P < 0.05], transfusion [OR = 0.15, 95% CI (0.08, 0.29), P < 0.01], positive surgical margin [OR = 0.73, 95% CI (0.55, 0.96), P < 0.05], postoperative complications [OR = 0.59, 95% CI (0.37, 0.95), P < 0.05], Clavien-Dindo > II complications [OR = 0.66, 95% CI (0.47, 0.94), P < 0.05], and intraoperative complications [OR = 0.51, 95% CI (0.26, 0.97), P < 0.05], but it had a longer operative time [WMD = 66.11, 95% CI (45.31, 86.90), P < 0.01]. The two surgical groups were comparable in terms of solid food intake time (p = 0.29), bowel obstruction (p = 0.36), and Clavien-Dindo I-II complications (p = 0.34). Postoperative long-term follow-up results showed that iRARC was superior in terms of 30-day complications [OR = 0.58, 95% CI (0.38, 0.88), P < 0.05], 90-day complications [OR = 0.67, 95% CI (0.58, 0.78), P < 0.01], 30-day Clavien-Dindo > II complications [OR = 0.66, 95% CI (0.52, 0.84), P < 0.05], 90-day Clavien-Dindo > II complications [OR = 0.77, 95% CI (0.63, 0.94), P < 0.01], 5-year cancer-specific survival [CSS HR = 0.71, 95% CI (0.51, 0.98), P < 0.05], and 5-year overall survival [OS HR = 0.73, 95% CI (0.60, 0.87), P < 0.01], but it had a higher incidence of ureteroenteric stricture [UES OR = 1.57, 95% CI (1.18, 2.09), P < 0.01]. The two surgical groups were comparable in terms of 30-day Clavien-Dindo I-II complications (p = 0.28), 90-day Clavien-Dindo I-II complications (p = 0.99), 30-day readmission (p = 0.68), 90-day readmission (p = 0.51), 90-day death (p = 0.37), recurrence (p = 0.18), 3-year CSS (p = 0.88), and 3-year OS (p = 0.19). CONCLUSION: Compared with ORC, iRARC was associated with improved perioperative outcomes, but attention should be paid to the monitoring and management of postoperative UES. Although improved 5-year OS and CSS were observed, these findings should be interpreted with caution because most of the available evidence was derived from observational studies and may have been influenced by residual confounding. Further large-scale, high-quality randomized controlled trials are needed to validate these findings.

Abstract as published, via PubMed.

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For healthcare professionals. The summary is generated by AI from the published abstract, and the evidence level is assigned automatically from the study design on the Oxford CEBM hierarchy. Neither is medical advice. Read the full paper before changing practice.