Long-Term Results of 2-Stage Turnbull-Cutait Pull-Through Coloanal Anastomosis for Low Rectal Cancer

Author:

Biondo Sebastiano1,Barrios Oriana1,Trenti Loris1,Espin Eloy2,Bianco Francesco3,Falato Armando4,De Franciscis Silvia5,Solis Alejandro2,Kreisler Esther1, ,Blanco Ana6,Golda Thomas6,Frago Ricardo6,Fraccalvieri Domenico6,Galvez Ana6,Verdaguer Mireia6,Alberti Piero A6,Miguel Bernat6

Affiliation:

1. Department of General and Digestive Surgery, Colorectal Unit, Bellvitge University Hospital, University of Barcelona and IDIBELL, Barcelona, Spain

2. Department of General and Digestive Surgery, Colorectal Unit, Vall d’Hebron University Hospital, Autonomic University of Barcelona, Barcelona, Spain

3. General and Colorectal Surgery Unit, S. Leonardo Hospital/ASL-Napoli 3-Sud, Castellammare di Stabia, Naples, Italy

4. General Surgery Unit, S. Giuliano Hospital, Giugliano, Naples, Italy

5. Colorectal Cancer Surgery Unit, Istituto Nazionale Tumori di Napoli, IRCCS, Naples, Italy

6. for the TURNBULL-BCN Study Group

Abstract

IMPORTANCEIn patients operated on for low rectal cancer, 2-stage Turnbull-Cutait pull-through hand-sewn coloanal anastomosis provides benefits in terms of postoperative morbidity compared with standard hand-sewn coloanal anastomosis associated with diverting ileostomy and further ileostomy reversal.OBJECTIVETo compare long-term results of these 2 techniques after ultralow rectal resection for rectal cancer.DESIGN, Setting, and ParticipantsIn this randomized multicenter clinical trial, neither patients nor surgeons were blinded for technique. Patients were recruited in 3 centers. Patients undergoing ultralow anterior rectal resection needing hand-sewn coloanal anastomosis were randomly assigned to 2-stage Turnbull-Cutait pull-through hand-sewn coloanal anastomosis (n = 46) or standard hand-sewn coloanal anastomosis associated with diverting ileostomy (n = 46).INTERVENTIONSAll patients underwent ultralow anterior resection. Patients assigned to the 2-stage Turnbull-Cutait pull-through group underwent exteriorization of a segment of left colon through the anal canal. After 6 to 10 days, the exteriorized colon was resected and a delayed hand-sewn coloanal anastomosis performed. For patients assigned to standard coloanal anastomosis, the hand-sewn coloanal anastomosis was performed with diverting ileostomy during the first operation. Ileostomy closure was scheduled after adjuvant treatment was completed in about 6 to 8 months.MAIN OUTCOME AND MEASUREThe study aimed to compare the differences between the 2 groups in terms of long-term surgery-related morbidity, functional, and oncological outcomes at 3 years postoperatively. Data were analyzed from October 1, 2018, through October 31, 2021.RESULTSThe 92 patients randomized in the first study were included for the 3-year follow-up. The overall morbidity rate in the 2 groups showed that 15 patients (16.3%) had complications with a difference of 6.52 (95% CI, −8.93 to 21.79). Nine patients (19.6%) and 6 patients (13.0%) in the 2-stage Turnbull-Cutait pull-through group and hand-sewn coloanal anastomosis group, respectively, had complications without statistically significant differences (P = .57). Oncological results were comparable between the groups. Long-term fecal continence in the CCA and TCA groups, respectively, assessed using the Wexner Incontinence Score was 10.9 (5.50-15.5) vs 13.0 (7.25-16.0; P = .92), Low Anterior Resection Syndrome score was 32.0 (21.0-37.0) vs 34.0 (23.2-38.5; P = .76), and Colorectal Functional Outcome score was 38.5 (23.0-47.1) vs 40.8 (23.3-58.2; P = .30).CONCLUSIONS AND RELEVANCEIn this study, after a 3-year follow-up period, 2-stage Turnbull-Cutait anastomosis for ultralow rectal cancer could be considered as a surgical alternative that has the valuable benefit of avoiding a temporary stoma with similar results in terms of morbidity, fecal continence, patient satisfaction, quality of life, and oncological outcomes when compared with hand-sewn coloanal anastomosis with ileostomy.TRIAL REGISTRATIONClinicalTrials.gov Identifier: NCT01766661

Publisher

American Medical Association (AMA)

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