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Open Versus Robot Assisted Radical Cystectomy With Totally Intracorporeal Urinary Diversion.

Open Versus Robot Assisted Radical Cystectomy With Totally Intracorporeal Urinary Diversion. Single Centre Prospective Randomized Trial.

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT03434132
Enrollment
116
Registered
2018-02-15
Start date
2018-01-29
Completion date
2022-09-30
Last updated
2023-01-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Bladder Cancer

Keywords

Open Radical Cystectomy, Robotic Radical cystectomy, Intracorporeal urinary diversion, Prospective randdomized trial

Brief summary

This prospective randomized study is designed to provide high level of evidence supporting superiority of robot assisted (RA) versus open (O) radical cystectomy (RC). The primary endpoint is a 50% reduction of transfusion rate, several perioperative outcomes potentially linked to a reduced invasiveness are considered as secondary endpoints. Investigators hypothesis is that the reduced invasiveness of RARC might turn into a higher adherence to enhanced recovery after surgery (ERAS) protocols (early bowel recovery, reduced need for painkillers and insertion of nasogastric tube) and consequently to shorter hospital stay and to faster return to daily activities. These data will be taken into account in a matched cost analysis between arms. Secondary aims include a between arm matched comparison of perioperative complications, oncologic outcomes (2-yr disease free survival is an accepted surrogate of long term oncologic effectiveness of RC) and functional outcomes (daytime and nighttime continence).

Detailed description

Despite encouraging data deriving from colorectal surgery, evidences in favor to ERAS protocols following RARC are poor. Moreover, according to a recent survey of surgeons with a specialist interest in RC, the adherence to ERAS protocols is \<20% \[1\]. Retrospective and preliminary data from the robotic consortium have supported oncologic effectiveness of RARC; however in the only prospective randomized trial comparing RARC and ORC urinary diversions were performed extracorporeally, potentially impairing the benefits of minimally invasive surgery \[2\]. Robot assisted radical cystectomy (RARC) has the aim of providing adequate cancer control while minimizing invasiveness of open radical cystectomy (ORC). The primary end-point of this trial is to demonstrate a reduction of perioperative transfusion rate in RARC arm by 50% compared to ORC arm. ERAS protocols may significantly contribute to shortening length of hospital stay, a key outcome in this clinical setting of patients receiving RC, being the mean length of hospital stay around 14 days in Italy. Investigators' hypothesis is that the reduced invasiveness of RARC might contribute to an increased adoption of ERAS protocols (reduced need for reinsertion of nasogastric tube, shorter time to first flatus, to mobilization, to regular diet and finally shorter duration of hospital stay). Assessment of oncologic outcomes of RARC, although not the primary endpoint of the present study, is certainly an outcome of interest. The expected duration of enrollment (18 mo) should provide 2-yr oncologic outcomes for about 66% of patients. Two-year recurrence free survival has been reported as a valid surrogate marker of long term oncologic survival after RC. Specific Aim 1:To demonstrate superiority of RARC versus ORC in terms of 50% reduction of perioperative transfusion rates. Specific Aim 2: To evaluate invasiveness of both surgical approaches by assessing the adherence to ERAS protocols in both and the incidence of perioperative and 30-d, 90d, 180d complications, readmission rates (30d, 90d). Cost analysis will assess the potential impact of shorter hospital stay on overall costs of robotic procedures. Specific Aim 3: To assess quality of life at 6-mo, 12-mo and 24-mo follow-up evaluation and to perform a matched comparison of oncologic and functional outcomes between two arms.

Interventions

PROCEDUREOpen or robotic radical cystectomy

ORC and orthotopic ileal neobladder is performed as previously described. A separate package PLND is performed as in open as in robotic surgery. RARC is performed replicating open surgical procedure. The orthotopic ileal neobladder model used is the 'vescica ileale padovana' as previously described. An ileal segment, approximately 42 cm long, is chosen at a minimum distance of 20cm far from ileo-cecal valve. A latero-lateral ileal anastomosis is performed with staplers to restore bowel continuity. For ileal conduit, a 20cm ileal segment (approximately 20 cm long) at a minimum distance of 20 cm from ileo-cecal valve is isolated and transected with staplers. Bowel continuity is restored as previously described. The ileal loop on its distal edge is extracted through abdomen wall at the previously identified stoma point and fixed to abdomen fascia. The ureters are spatulated and a latero-lateral anastomosis according to Wallace 1 technique is performed.

Sponsors

Ministero della Salute, Italy
CollaboratorOTHER
Regina Elena Cancer Institute
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* Patients with muscle invasive high grade urothelial carcinoma (and variant histologies) of the bladder or high grade non muscle invasive BCG recurrent/refractory disease.

Exclusion criteria

* Cystectomy without curative intent (palliative, salvage). * Patients unfit for robotic cystectomy.

Design outcomes

Primary

MeasureTime frameDescription
Number of participants requiring perioperative transfusions.30 days50% reduction of perioperative transfusion rates in robotic arm.

Secondary

MeasureTime frameDescription
Incidence of Clavien grade 1-2 perioperative complications at 30-d evaluation.30 daysComparison between open and robotic arms.
Incidence of Clavien grade 1-2 perioperative complications at 90-d evaluation.90 daysComparison between open and robotic arms.
Number of participants requiring insertion of nasogastric tube30 daysComparison between open and robotic arms.
Incidence of patients requiring readmission.90 daysComparison between open and robotic arms.
Cost analysis.30 daysComparison between open and robotic arms.
Incidence of Clavien grade 1-2 perioperative complications at 180-d evaluation.180 daysComparison between open and robotic arms.

Other

MeasureTime frameDescription
Cancer specific survival24 monthsComparison between open and robitic arms
Assessment of quality of life at 6-mo follow-up with self-administered EORTC QLQ-BLM30 questionnaire6 monthsComparison between open and robotic arms.
Assessment of urinary continence with pad test.12 monthsComparison between open and robotic arms
Overall survival24 monthsComparison between open and robitic arms
Assessment of quality of life at 6-mo follow-up with self-administered EORTC QLQ-C30 questionnaire6 monthsComparison between open and robotic arms.
Assessment of quality of life at 12-mo follow-up with self-administered EORTC QLQ-BLM30 questionnaire12 monthsComparison between open and robotic arms.
Assessment of quality of life at 12-mo follow-up with self-administered EORTC QLQ-C30 questionnaire12 monthsComparison between open and robotic arms.
Assessment of quality of life at 24-mo follow-up with self-administered EORTC QLQ-BLM30 questionnaire24 monthsComparison between open and robotic arms.
Assessment of quality of life at 24-mo follow-up with self-administered EORTC QLQ-C30 questionnaire24 monthsComparison between open and robotic arms.
Disease free survival24 monthsComparison between open and robitic arms

Countries

Italy

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 23, 2026