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Transanal Versus Laparoscopic Total Mesorectal Excision for Rectal Cancer

Transanal Versus Laparoscopic Total Mesorectal Excision for Mid and Low Rectal Cancer (TaLaR): a Multicentre Randomised Clinical Trial

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02966483
Enrollment
1114
Registered
2016-11-17
Start date
2016-04-30
Completion date
2026-07-31
Last updated
2025-01-17

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

Conditions

Rectal Neoplasms Malignant, Surgery

Keywords

Rectal cancer, Laparoscopic surgery, Total mesorectal excision, Transanal, Multicentre randomised clinical trial

Brief summary

Laparoscopic surgery for rectal cancer has been successfully proven to be a non-inferior alternative regarding resection quality, and oncological outcomes of patients as compared to open surgery in mangy clinical trails. Moreover, laparoscopic surgery is advantageous over open surgery with regard to operative invasiveness, patient's recovery, and wound related complications. Thus, laparoscopic surgery has gained great popularity over the past decades. However, specifically for mid and low rectal cancer, laparoscopic surgery is technically demanding, which sometimes leads to high morbidity and unsatisfactory resection quality, especially in challenging cases such as bulky mesorectum, enlarged prostate, irradiated pelvis, etc. Under this circumstance, transanal total mesorectal excision (TaTME) , the so called down-to-up alternative, has emerged as a promising solution to these problems in recent years and more and more small studies have proven the feasibility and advantages of this technique, making it become a hot topic among both literature and conferences. However, TaTME is still at early birth, higher-level evidences, either multicentric, or comparative study with conventional surgery is strikingly lacking. Thus the investigators conduct this multicentre randomised clinical trial, comparing transanal TME versus laparoscopic TME for mid and low rectal cancer, aiming to prove the hypothesis that TaTME may achieve better resection quality and result in non-inferior oncological outcome, as well as short term operative morbidity and mortality.

Detailed description

Background:In recent years, transanal mesorectal excision (TaTME) has emerged as a promising surgical alternative for rectal cancer, especially for mid and low rectal cancer. Theoretically, TaTME holds the potential advantage of providing better access to mobilize the distal rectum, and thus could achieve better pathologic outcomes, such as lower involved circumferential margin (CRM) and incomplete resected mesorectum, which could translate into better oncological outcome for the patients in the long term. However, until now, the feasibility and the non-inferiority (compared with laparoscopic total mesorectal excision, LpTME) of this technique has only been validated in studies with limitations of small sample size, retrospective nature. Study Objective:This study aims to evaluate the TaTME technique compared with conventional laparoscopic rectal surgery, focusing on resection quality, as well as long-term survival results. Study design This study is a prospective, multi-center, randomized, open-label, parallel group trial. The randomisation ratio of TaTME over LpTME will be 1:1. A central electronic data capture (EDC) system will be utilized for randomization, electronic CRF and data collection. All comparative analyses will be conducted on an intention to treat basis. Sample size: Sample-size calculation of this trial based on 3-year DFS and 5-year OS; but the sample size according to 5-year OS was larger than that based on 3-year DFS. The expected 5-year OS among clinical stage I-III rectal cancer patients treated with laTME was 77·4%. Allowing a difference of 10% as the non-inferiority margin, 910 patients would be required to sufficiently declare taTME noninferior to laTME in 5-year OS based on a log-rank test with an α error of 2·5% (in a two-sided test) and power of 80%. Assuming a dropout rate of 20%, a total of 1114 patients were planned to enroll for this trial. Study Endpoints:The primary end point of this study is 3-year disease-free survival (DFS) rate and a 5-year overall survival (OS) rate. Secondary endpoints include: 1) resection quality, mainly including circumferential involvement rate, and completeness of mesorectum. Resected specimen was pathologically processed and assessed at each center by trained and qualified pathologists independently.2)short term operative results such as morbidity and mortality, etc.; 3) long term oncological outcome such as local recurrence, and overall survival. Besides, functional outcome and quality of life are also evaluated.

Interventions

PROCEDURETaTME

Transanal Total Mesorectal Excision

PROCEDURELpTME

Conventional Laparoscopic Total Mesorectal Excision

Sponsors

Peking Union Medical College Hospital
CollaboratorOTHER
The First Hospital of Jilin University
CollaboratorOTHER
RenJi Hospital
CollaboratorOTHER
Shengjing Hospital
CollaboratorOTHER
The Second People's Hospital of Yibin
CollaboratorOTHER
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University
CollaboratorOTHER
Nanchong Central Hospital
CollaboratorOTHER_GOV
Zunyi Medical College
CollaboratorOTHER
The First Affiliated Hospital of University of South China
CollaboratorOTHER
Xinqiao Hospital
CollaboratorUNKNOWN
Nanfang Hospital, Southern Medical University
CollaboratorOTHER
First Affiliated Hospital Xi'an Jiaotong University
CollaboratorOTHER
Ruijin Hospital
CollaboratorOTHER
Affiliated Hospital of Guangdong Medical University
CollaboratorOTHER
The Third Xiangya Hospital of Central South University
CollaboratorOTHER
Sun Yat-sen University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

Transanal or Laparoscopic Total Mesorectal Excision treat rectal cancer

Eligibility

Sex/Gender
ALL
Age
18 Years to 75 Years
Healthy volunteers
No

Inclusion criteria

histologically proven rectal adenocarcinoma; tumor located below the level of peritoneal reflection ; diagnosis of rectal cancer amenable to curative surgery; no evidence of distant metastases; preoperative tumor stage within III; no threaten mesorectal fascia (MRF)after neoadjuvant therapy; no contraindication to laparoscopic surgery; without history of other malignancies; Written informed consent

Exclusion criteria

could not perform sphincter preservation surgery (requiring a Mile's procedure); T4b tumor invading adjacent organs; T1 tumors that can be locally resected should take neoadjuvant therapy but refuse it; recurrent cancer; concurrent or previous diagnosis of invasive cancer within 5 years; emergent surgery with intestinal obstruction or perforation; history of colorectal surgery; fecal incontinence; history of inflammatory bowel disease; with contraindications to general anaesthesia(ASA class 4 or 5); pregnant or breast-feeding; history of mental disorder

Design outcomes

Primary

MeasureTime frameDescription
Disease-free survival3 yearsDisease-free survival
Overall survival5 yearsOverall survival

Secondary

MeasureTime frameDescription
Positive circumferential resection margin (CRM)3 yearsInvolved CRM (tumor cells \<1mm)
Overall survival10 yearsOverall survival
Mesorectal completeness3 yearsThe quality of the mesorectum or TME specimen (complete;nearly complete; incomplete)
Sexual functional outcomes3 yearsTo evaluate sexual function with IIEF(International Index of Erectile Function) questionnaire
Morbidity rate1 yearsMorbidity rate
Mortality rate1 yearsMortality rate
Anorectal function outcomes3 yearsTo evaluate defecating function with Wexner score
Number of retrieved lymph nodes3 yearsNumber of retrieved lymph nodes
The patient's Quality of life: EORTC QLQ-30 questionnaire3 yearsTo evaluate quality of life with EORTC QLQ-30 questionnaire

Countries

China

Contacts

Primary ContactLiang Kang, MD,PHD
eonkang@163.com008613602886833

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 1, 2026