Oncologic Equipoise Between Robotic and Open Radical Cystectomy.

Journal: Journal of endourology
Published Date:

Abstract

Our objective was to establish the incidence of positive surgical margins, recurrence patterns, and recurrence-free (RFS) and overall survival (OS) in a large cohort of patients undergoing robotic (robot-assisted radical cystectomy [RARC]) and open radical cystectomy (ORC). We performed a large retrospective cohort study at a high-volume academic tertiary referral center. Patients were those who underwent RC for bladder cancer from 2005 to 2017. Patients were allocated to ORC or RARC by patient and surgeon choice. Propensity matching and a multivariable analysis were performed to determine factors predictive of RFS and OS after RC. All analyses were done with SAS 9.4. The study included 1885 patients, 13.5% of whom underwent RARC. There was no difference in positive soft tissue surgical margins (2.4% in ORC and 1.2% in RARC). There were no differences in recurrence patterns, nor in the severity of pathology distribution between the two cohorts. Peritoneal carcinomatosis was seen in 1.1% of ORC and 0.8% in RARC. Shorter RFS was associated with younger age (hazard ratio [HR] 1.04, 95% confidence interval [CI] 1.03-1.05,  < 0.001), neoadjuvant chemotherapy (HR 1.41, 95% CI 1.14-1.75,  = 0.002), higher pathologic stage (stage ≥T HR 2.45, 95% CI 1.91-3.16,  < 0.001), lymph node positivity at cystectomy (HR 1.92, 95% CI 1.50-2.47,  < 0.001), and positive surgical margins (HR 1.49, 95% CI 1.09-2.05,  = 0.01). RFS and OS did not differ by surgical approach (HR 1.04, 95% CI 0.83-1.30),  = 0.75 and (HR 0.89, 95% CI 0.67-1.19),  = 0.43, respectively. The data from this study support continued use of RARC as a safe oncologic procedure, with similar outcomes to ORC.

Authors

  • Janet Baack Kukreja
    University of Colorado Cancer Center, Aurora, CO.
  • Roger Li
    Department of Urology, H. Lee Moffitt Cancer Center and Research Institute, Tampa, FL.
  • Vikram M Narayan
    Department of Urology, Division of Surgery, University of Texas MD Anderson Cancer Center, Houston, TX.
  • Amy Lim
    Department of Urology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Mohamed Seif
    Department of Urology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Xuemei Wang
    Department of Biostatistics, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Ashish Kamat
    Department of Urology, University of Texas MD Anderson Cancer Center, Houston, Texas, USA.
  • Colin Dinney
    Department of Urology, Division of Surgery University of Texas MD Anderson Cancer Center Houston TX USA.
  • Neema Navai
    Department of Urology, Division of Surgery University of Texas MD Anderson Cancer Center Houston TX USA.