Rectal Surgery Evaluation Trial: protocol for a parallel cohort trial of outcomes using surgical techniques for total mesorectal excision with low anterior resection in high-risk rectal cancer patients.
Adult
Aged
Comparative Effectiveness Research
Female
Humans
Laparoscopy
/ methods
Laparotomy
/ methods
Length of Stay
Male
Margins of Excision
Middle Aged
Observational Studies as Topic
Operative Time
Postoperative Complications
/ etiology
Proctectomy
/ methods
Prospective Studies
Quality of Life
Rectal Neoplasms
/ surgery
Rectum
/ surgery
Robotic Surgical Procedures
/ methods
Transanal Endoscopic Surgery
/ methods
Treatment Outcome
laparoscopy
laparotomy
rectal cancer
robot-assisted surgery
transanal surgery
Journal
Colorectal disease : the official journal of the Association of Coloproctology of Great Britain and Ireland
ISSN: 1463-1318
Titre abrégé: Colorectal Dis
Pays: England
ID NLM: 100883611
Informations de publication
Date de publication:
05 2019
05 2019
Historique:
received:
20
07
2018
accepted:
02
02
2019
pubmed:
12
2
2019
medline:
26
9
2020
entrez:
12
2
2019
Statut:
ppublish
Résumé
Total mesorectal excision (TME) is the standard of care for rectal cancer, which can be combined with low anterior resection (LAR) in patients with mid-to-low rectal cancer. The narrow pelvic space and difficulties in obtaining adequate exposure make surgery technically challenging. Four techniques are used to perform the surgery: open laparotomy, laparoscopy, robot-assisted surgery and transanal surgery. Comparative data for these techniques are required to provide clinical data on the surgical management of rectal cancers. The Rectal Surgery Evaluation Trial will be a prospective, observational, case-matched, four-cohort, multicentre trial designed to study TME with LAR using open laparotomy, laparoscopy, robot-assisted surgery or transanal surgery in high-surgical-risk patients with mid-to-low non-metastatic rectal cancer. All surgeries will be performed by surgeons experienced in at least one of the techniques. Oncological, morbidity and functional outcomes will be assessed in a composite primary outcome, with success defined as circumferential resection margin ≥ 1 mm, TME Grade III and minimal postoperative morbidity (absence of Clavien-Dindo Grade III-IV complications within 30 days after surgery). Secondary end-points will include the co-primary end-points over the long term (2 years), quality of surgery, quality of life, length of hospital stay, operative time and rate of unplanned conversions. This will be the first trial to study all four surgical techniques currently used for TME with LAR in a specific group of high-risk patients. The knowledge obtained will contribute towards helping physicians determine the advantages of each technique and which may be the most appropriate for their patients.
Types de publication
Clinical Trial Protocol
Journal Article
Multicenter Study
Langues
eng
Sous-ensembles de citation
IM
Pagination
516-522Informations de copyright
Colorectal Disease © 2019 The Association of Coloproctology of Great Britain and Ireland.