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Robot-assisted Esophagectomy Versus Conventional Thoracoscopic Esophagectomy (RAE vs CTE)

Primary Purpose

Esophageal Cancer, Esophageal Carcinoma

Status
Recruiting
Phase
Phase 3
Locations
China
Study Type
Interventional
Intervention
esophagectomy
esophagectomy
Sponsored by
Shanghai Chest Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophageal Cancer focused on measuring robot assisted esophagectomy, minimally invasive esophagectomy, esophageal cancer

Eligibility Criteria

18 Years - 75 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Histologically proven squamous cell carcinoma of the intrathoracic esophagus.
  • Surgical resectable (T1b-3, N0-2, M0)
  • Age ≥ 18 and ≤ 75 years
  • European Clinical Oncology Group performance status 0, 1 or 2
  • Written informed consent

Exclusion Criteria:

  • Carcinoma of the cervical esophagus
  • Histologically proven adenocarcinoma or undifferentiated carcinoma.
  • Prior thoracic surgery at the right hemithorax or thorax trauma.
  • Infectious disease with systemic therapy indicated.

Sites / Locations

  • General hospital of eastern theater commandRecruiting
  • The First Affiliated Hospital of Nanchang UniversityRecruiting
  • Changhai Hospital, The Second Military Medical UniversityRecruiting
  • Ruijin Hospital, Shanghai Jiao Tong University, School of MedicineRecruiting
  • Shanghai Chest Hospital, Shanghai Jiao Tong UniversityRecruiting
  • Zhongshan Hospital, Fudan UniversityRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Robot assisted esophagectomy

Thoracoscopic esophagectomy

Arm Description

Robot-assisted esophagectomy with gastric conduit formation.

Conventional thoracoscopic esophagectomy with gastric conduit formation.

Outcomes

Primary Outcome Measures

Overall Survival Rate

Secondary Outcome Measures

R0 resection (%)
Overall Survival Rate
Disease Free Survival Rate
Postoperative major complications
In hospital mortality
For all patients, the cause of death will be noted. If applicable, the results of the autopsy report will be noted.
Operative duration
The operation time is defined as time from incision until closure (minutes) for both the thoracic phase and the abdominal phase of the procedure. For the robotic procedure, the set-up time will be recorded separately.
Postoperative recovery
Postoperative hospital stay, intensive care unit (ICU) stay
Number of lymph nodes dissected
Quality of life
The quality of life assessment was based on a previously validated questionnaire, QLQ-C30 (version 3.0; quality-of-life questionnaire), combined with an esophageal cancer-specific module, QLQ-OES18.
Estimated blood loss
Disease Free Survival Rate

Full Information

First Posted
March 20, 2017
Last Updated
February 3, 2020
Sponsor
Shanghai Chest Hospital
Collaborators
Ruijin Hospital, Changhai Hospital, Shanghai Zhongshan Hospital, The First Affiliated Hospital of Nanchang University
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1. Study Identification

Unique Protocol Identification Number
NCT03094351
Brief Title
Robot-assisted Esophagectomy Versus Conventional Thoracoscopic Esophagectomy
Acronym
RAE vs CTE
Official Title
Robot-assisted Esophagectomy Versus Conventional Thoracoscopic Esophagectomy for Patients With Squamous Cell Esophageal Cancer: a Multicenter Open-label, Randomized Controlled Trial (RAMIE Trial)
Study Type
Interventional

2. Study Status

Record Verification Date
February 2019
Overall Recruitment Status
Recruiting
Study Start Date
July 29, 2017 (Actual)
Primary Completion Date
December 1, 2024 (Anticipated)
Study Completion Date
December 1, 2024 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shanghai Chest Hospital
Collaborators
Ruijin Hospital, Changhai Hospital, Shanghai Zhongshan Hospital, The First Affiliated Hospital of Nanchang University

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No

5. Study Description

Brief Summary
This is the first randomized controlled study to compare the robot-assisted esophagectomy (RAE) to minimally invasive conventional thoracoscopic esophagectomy (CTE). The aim of this trial is to evaluate the safety, risks of the robot-assisted esophagectomy, and to compare the short-term operative outcomes and long-term oncological outcomes between the two surgical treatments.
Detailed Description
Objective: This study aims to compare the oncological outcomes between robot-assisted esophagectomy and minimally invasive conventional thoracoscopic esophagectomy. Study design: Randomized controlled parallel-group superiority trial Study population: Patients (age >= 18 and <= 75 years) with histologically proven surgically resectable (cT1b-3, N0-2, M0) squamous cell carcinoma of the intrathoracic esophagus with European Clinical Oncology Group performance status 0, 1 or 2. Intervention: 360 patients will be randomly allocated to either A) robot-assisted esophagectomy (n=180) or B) conventional thoracoscopic esophagectomy (n=180). Patients will receive the following interventions: Group A. robot assisted esophagectomy, with gastric conduit formation. Group B. conventional thoracoscopic esophagectomy, with gastric conduit formation. Main study parameters/endpoints: Primary outcome is 5-year overall survival rate. Secondary outcomes are 5-year disease free survival, 3-year overall survival rate, 3-year disease free survival, (in hospital) mortality within 30 and 60 days, R0 resections, operation related events, postoperative recovery, lymph nodes status, quality of life. Follow-up: 60 months after discharge of the last randomized patient.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Cancer, Esophageal Carcinoma
Keywords
robot assisted esophagectomy, minimally invasive esophagectomy, esophageal cancer

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Model Description
Parallel Assignment
Masking
None (Open Label)
Masking Description
Open Label
Allocation
Randomized
Enrollment
360 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Robot assisted esophagectomy
Arm Type
Experimental
Arm Description
Robot-assisted esophagectomy with gastric conduit formation.
Arm Title
Thoracoscopic esophagectomy
Arm Type
Active Comparator
Arm Description
Conventional thoracoscopic esophagectomy with gastric conduit formation.
Intervention Type
Procedure
Intervention Name(s)
esophagectomy
Other Intervention Name(s)
minimally invasive esophagectomy
Intervention Description
Robot assisted esophagectomy with extended two field lymphadenectomy.
Intervention Type
Procedure
Intervention Name(s)
esophagectomy
Other Intervention Name(s)
minimally invasive esophagectomy
Intervention Description
Conventional thoracoscopic esophagectomy with extended two field lymphadenectomy.
Primary Outcome Measure Information:
Title
Overall Survival Rate
Time Frame
5 years
Secondary Outcome Measure Information:
Title
R0 resection (%)
Time Frame
within 30 days after surgery
Title
Overall Survival Rate
Time Frame
3 years
Title
Disease Free Survival Rate
Time Frame
3 years
Title
Postoperative major complications
Time Frame
30 days after surgery
Title
In hospital mortality
Description
For all patients, the cause of death will be noted. If applicable, the results of the autopsy report will be noted.
Time Frame
30-60 days after surgery
Title
Operative duration
Description
The operation time is defined as time from incision until closure (minutes) for both the thoracic phase and the abdominal phase of the procedure. For the robotic procedure, the set-up time will be recorded separately.
Time Frame
during the operation, up to 5 hours
Title
Postoperative recovery
Description
Postoperative hospital stay, intensive care unit (ICU) stay
Time Frame
from the date of surgery to the hospital discharge, assessed up to 15 days
Title
Number of lymph nodes dissected
Time Frame
within 30 days after surgery
Title
Quality of life
Description
The quality of life assessment was based on a previously validated questionnaire, QLQ-C30 (version 3.0; quality-of-life questionnaire), combined with an esophageal cancer-specific module, QLQ-OES18.
Time Frame
2 years
Title
Estimated blood loss
Time Frame
during the operation, up to 5 hours
Title
Disease Free Survival Rate
Time Frame
5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Histologically proven squamous cell carcinoma of the intrathoracic esophagus. Surgical resectable (T1b-3, N0-2, M0) Age ≥ 18 and ≤ 75 years European Clinical Oncology Group performance status 0, 1 or 2 Written informed consent Exclusion Criteria: Carcinoma of the cervical esophagus Histologically proven adenocarcinoma or undifferentiated carcinoma. Prior thoracic surgery at the right hemithorax or thorax trauma. Infectious disease with systemic therapy indicated.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Zhigang Li, Master
Phone
86-18930619260
Email
zhigang.li@shchest.org
First Name & Middle Initial & Last Name or Official Title & Degree
Xiaobin Zhang, Doctor
Phone
86-18516302162
Email
zxb5212@163.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Zhigang Li, Master
Organizational Affiliation
Shanghai Chest Hospital, Shanghai Jiao Tong University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Hecheng Li, Master
Organizational Affiliation
Ruijin Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Hezhong Chen, Master
Organizational Affiliation
Changhai Hospital, the Second Military Medical University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Lijie Tan, Master
Organizational Affiliation
Fudan University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Bentong Yu, Master
Organizational Affiliation
The First of Affiliated Hospital of Nanchang University
Official's Role
Study Director
Facility Information:
Facility Name
General hospital of eastern theater command
City
Nanjing
State/Province
Jiangsu
ZIP/Postal Code
JS 25
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jun Yi, Doctor
Phone
8613675101301
Email
njyijun@163.com
Facility Name
The First Affiliated Hospital of Nanchang University
City
Nanchang
State/Province
Jiangxi
ZIP/Postal Code
JX 791
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Bentong Yu, Doctor
Phone
86-13870614026
Email
yubentong@126.com
Facility Name
Changhai Hospital, The Second Military Medical University
City
Shanghai
ZIP/Postal Code
SH 21
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hezhong Chen, Doctor
Phone
86-13301783183
Email
drchenhz@citiz.net
Facility Name
Ruijin Hospital, Shanghai Jiao Tong University, School of Medicine
City
Shanghai
ZIP/Postal Code
SH 21
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Hecheng Li, Doctor
Phone
86-13917113402
Email
lihecheng2000@hotmail.com
Facility Name
Shanghai Chest Hospital, Shanghai Jiao Tong University
City
Shanghai
ZIP/Postal Code
SH 21
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Zhigang Li, Doctor
Phone
86-18930619260
Email
zhigang.li@shchest.org
Facility Name
Zhongshan Hospital, Fudan University
City
Shanghai
ZIP/Postal Code
SH 21
Country
China
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Lijie Tan, Doctor
Phone
86-13681972151
Email
tan.lijie@zs-hospital.sh.cn

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34171870
Citation
Yang Y, Li B, Yi J, Hua R, Chen H, Tan L, Li H, He Y, Guo X, Sun Y, Yu B, Li Z. Robot-assisted Versus Conventional Minimally Invasive Esophagectomy for Resectable Esophageal Squamous Cell Carcinoma: Early Results of a Multicenter Randomized Controlled Trial: the RAMIE Trial. Ann Surg. 2022 Apr 1;275(4):646-653. doi: 10.1097/SLA.0000000000005023.
Results Reference
derived
PubMed Identifier
31226960
Citation
Yang Y, Zhang X, Li B, Li Z, Sun Y, Mao T, Hua R, Yang Y, Guo X, He Y, Li H, Chen H, Tan L. Robot-assisted esophagectomy (RAE) versus conventional minimally invasive esophagectomy (MIE) for resectable esophageal squamous cell carcinoma: protocol for a multicenter prospective randomized controlled trial (RAMIE trial, robot-assisted minimally invasive Esophagectomy). BMC Cancer. 2019 Jun 21;19(1):608. doi: 10.1186/s12885-019-5799-6.
Results Reference
derived

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Robot-assisted Esophagectomy Versus Conventional Thoracoscopic Esophagectomy

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