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Open Versus Laparoscopic Complete Mesocolic Excision for Locally Advanced Colon Cancer

A Multicenter, Prospective, Randomized Clinical Trial to Investigate Open Versus Laparoscopic Complete Mesocolic Excision for Locally Advanced Colon Cancer

Status
UNKNOWN
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT02682589
Acronym
OLCMECC
Enrollment
1080
Registered
2016-02-15
Start date
2016-04-30
Completion date
2023-04-30
Last updated
2016-07-06

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

Conditions

Colon Cancer

Keywords

Complete Mesocolic Excision, locally advanced Colon Cancer, Laparoscopic

Brief summary

Randomized, multicenter, phase III trial to compare the short and long outcomes of laparoscopic CME with open CME in treating patients with locally advanced colon cancer.

Detailed description

Laparoscopic complete mesocolic excision (CME) in treating colon cancer has been reported to be feasible and safe and holds many advantages when compared with traditional open surgery, such as reducing preoperative blood loss, alleviating postoperative pain and reducing complications and length of hospital stay. Whether laparoscopic CME could achieve an equivalent oncological outcome, especially for locally advanced malignancy, is still being discussed. The purpose of this study is to determine the short and long outcomes of open and laparoscopic CME for locally advanced colon cancer patients. The primary endpoint is the 5-year disease-free survival rate. Secondary endpoints include completeness of mesocolon, morbidity and mortality, local recurrence, overall survival, quality of life et al. In this study, eligible patient will be randomly allocated to receive either open or laparoscopic CME surgery. Randomization will be performed centrally and be stratified for age, gender, T-stage, tumor location. Patients will be randomized in a 2:1 ratio, in favor of the laparoscopic CME. The extent of resection according to CME principle is identical for both arms. CME involves the removal of the afflicted colon and its accessory lymphvascular supply at their origins by resecting the colon and mesocolon in an intact envelope of visceral peritoneum and mesenteric fascia. Type of anastomosis, location of auxiliary incision and drainage of surgical field are up to the discretion of the surgeon. In laparoscopic surgery, a medial-to-lateral approach and a no-touch isolation are required . Intraoperative pictures were taken at various stages, as were photographs of the postoperative specimen, which will be assessed by a third-party expert to qualify the surgery. The baseline demographics and conditions as well as the perioperative and postoperative outcomes will be recorded through a prior designed format. Our study is expected to last seven years, of which two years for recruiting patients, five years for follow-up. Patients are followed up every 3 months for 2 year, every 6 months for 3 years postoperatively.

Interventions

PROCEDUREOpen surgery

A traditional midline incision is made through the abdominal wall and a colectomy with CME is performed.

PROCEDURELaparoscopic surgery

3-5 small incisions are made through the abdominal wall for the placement of trocars and the abdominal cavity is insufflated with carbon dioxide to allow access, visualization and operation. A 6-8cm auxiliary incision is made for specimen extraction and anastomosis. Conversion may occur due to technical difficulties or intraoperative complications, which is defined when completion of the dissection of the mesocolon is performed through a traditional open abdominal approach. Patients undergo conversion to laparotomy will be excluded from this study.

Sponsors

West China Hospital
CollaboratorOTHER
Changhai Hospital
CollaboratorOTHER
Chinese PLA General Hospital
CollaboratorOTHER
Peking Union Medical College Hospital
CollaboratorOTHER
Ruijin Hospital
CollaboratorOTHER
RenJi Hospital
CollaboratorOTHER
Shanghai Changzheng Hospital
CollaboratorOTHER
Union Hospital, Tongji Medical College, Huazhong University of Science and Technology
CollaboratorOTHER
Fujian Medical University
CollaboratorOTHER
First Affiliated Hospital of Chongqing Medical University
CollaboratorOTHER
The First Affiliated Hospital with Nanjing Medical University
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Eligibility

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

Inclusion criteria

* Patients suitable for curative surgery over 18 years old; * American Society of Anesthesiologists(ASA) grade I-III; * Pathological diagnosis of adenocarcinoma; * Tumor located between the cecum and sigmoid colon; * Enhanced CT scan of chest, abdominal and pelvic cavity: preoperative assessment of tumor stage is T3-T4 N0 or T any N+ (according to the National Comprehensive Cancer Network(NCCN) clinical practice guidelines in oncology: colon cancer version 2.2015);there is no distant metastasis; * Informed consent; * No preoperative chemoradiotherapy; * No history of familial adenomatous polyposis, ulcerative colitis or Crohn's disease.

Exclusion criteria

* Pregnant patient; * History of psychiatric disease; * Use of systemic steroids; * Conversion to laparotomy; * Simultaneous or simultaneous multiple primary colorectal cancer; * Preoperative imaging examination results show: 1. Tumor involves the surrounding organs and combined organ resection need to be done; 2. distant metastasis; 3. unable to perform R0 resection; * Postoperative pathology of T1-T2 N0; * History of any other malignant tumor in recent 5 years; * Patients need emergency operation: mechanic ileus, perforation. * Not suitable for laparoscopic surgery (i.e., extensive adhesion caused by abdominal surgery, not suitable for artificial pneumoperitoneum, etc).

Design outcomes

Primary

MeasureTime frame
disease-free survival5 years

Secondary

MeasureTime frameDescription
overall survival5 years
recurrence-free survival5 years
local recurrence rate5 years
length of postoperative hospital stay30 daysLength of postoperative hospital stay is defined as a duration between surgery and first discharge. An expected average is 10 days.
early complication rate30 daysEarly complication is defined as a complication that occurred between the finish of the surgery and postoperative day 30. Complications includes anastomotic leakage, anastomotic bleeding, chyle leakage, wound infection, pulmonary embolism, myocardial infarction et al.The Clavien-Dindo Classification of Surgical Complications will be applied to access the degree of severity of postoperative complications.
operative time1 day
completeness of the mesocolon of the specimen1 dayA central review by pathologists to define the completeness of the mesocolon to be good, moderate or poor will be performed on the specimen photographs.
number of lymph nodes retrieved1 day
postoperative quality of life as assessed by EORTC QLQ-C30 questionnaire5 yearsCompare the differences in postoperative quality of life of patients treated with these two regimens using EORTC QLQ-C30 questionnaire

Countries

China

Contacts

Primary ContactYueming Sun, PhD
jssym@vip.sina.com02568136026

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026