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Mediastinoscopy-assisted Transhiatal Esophagectomy Versus Thoraco-laparoscopic Esophagectomy for Esophageal Cancer

Primary Purpose

Esophageal Neoplasms

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Thoraco-laparoscopic esophagectomy
Mediastinoscopy-assisted transhiatal esophagectomy
Sponsored by
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Esophageal Neoplasms focused on measuring Mediastinoscopy-assisted transhiatal esophagectomy (MATHE), Thoraco-laparoscopic esophagectomy (TLE)

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • 18 years≤age≤ 80 years;
  • Histologically diagnosed with squamous cell carcinoma by endoscopic biopsy, cT1-3N0M0;
  • Primary tumour is located in the thoracic oesophagus
  • No clinical evidence of distant organ metastasis
  • No severe comorbidity, can tolerate anesthesia;
  • ECOG PS scores≤2;
  • The patients sign informed consents by themselves.

Exclusion Criteria:

  • Cervical or abdominal oesophageal carcinoma;
  • Previous oesophagectomy, gastrectomy, or mediastinal surgery;
  • Current uncontrolled illness such as severe cardiac disease, uncontrollable hypertension or diabetes, or active bacterial infection;
  • Unable to tolerate tracheal intubation and general anaesthesia as determined by an anaesthesiologist preoperatively;
  • Pregnant or lactating women;
  • ECOG PS scores>2;
  • Considered unsuitable, such as those who do not agree to participate in the trial.

Sites / Locations

  • Cancer Hospital of Chinese Academy of Medical Sciences Shenzhen Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

Thoraco-laparoscopic esophagectomy

Mediastinoscopy-assisted transhiatal esophagectomy

Arm Description

Treated by thoraco-laparoscopic esophagectomy in the centers with enough experience in esophageal resection and the volume ≧80 cases each year.

Treated by mediastinoscopy-assisted transhiatal esophagectomy in the centers with enough experience in esophageal resection and the volume ≧80 cases each year.

Outcomes

Primary Outcome Measures

Postoperative respiratory complications
These respiratory complications involve respiratory distress or failure after the operation with continuation of mechanical ventilation, pulmonary atelectasis requiring sputum suction by bronchoscopy, pneumonia requiring specific antibiotics confirmed by thoracic X-ray or CT scan of the thorax and a positive sputum culture, and acute respiratory distress syndrome.

Secondary Outcome Measures

pulmonary function indicators
pulmonary function indicators
anastomotic fistula
anastomotic fistula
recurrent laryngeal nerve palsy
recurrent laryngeal nerve palsy
DFS
Disease-free survival,DFS
duration of surgery
Total operation time
Blood loss
blood loss during the surgery
Conversion rate
conversion to thoracotomy during surgery
postoperative hospital stay
postoperative hospital stay
postoperative pain score
postoperative pain score
drainage time
drainage time
R0 resection rate
R0 resection rate
Lymph node dissection
During the surgery, lymph node dissection were performed. The number of removed lymph-nodes were recorded according to the postoperative pathological diagnosis, and the stations of the lymph node were recorded.
Local recurrence
three-year local tumour recurrence or distant metastasis rate after surgery
30-day mortality after surgery
30-day mortality after surgery

Full Information

First Posted
October 11, 2019
Last Updated
April 12, 2020
Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Collaborators
Peking University Cancer Hospital & Institute, Hubei Cancer Hospital, The First Affiliated Hospital of Anhui Medical University, Quanzhou First Hospital, The People's Hospital of Gaozhou, The Second People's Hospital of Huai'an
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1. Study Identification

Unique Protocol Identification Number
NCT04125849
Brief Title
Mediastinoscopy-assisted Transhiatal Esophagectomy Versus Thoraco-laparoscopic Esophagectomy for Esophageal Cancer
Official Title
Mediastinoscopy-assisted Transhiatal Esophagectomy (MATHE) Versus Thoraco-laparoscopic Esophagectomy (TLE) for Esophageal Cancer: a Multicenter Randomized Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
April 2020
Overall Recruitment Status
Unknown status
Study Start Date
April 2020 (Anticipated)
Primary Completion Date
December 2021 (Anticipated)
Study Completion Date
December 2022 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Cancer Institute and Hospital, Chinese Academy of Medical Sciences
Collaborators
Peking University Cancer Hospital & Institute, Hubei Cancer Hospital, The First Affiliated Hospital of Anhui Medical University, Quanzhou First Hospital, The People's Hospital of Gaozhou, The Second People's Hospital of Huai'an

4. Oversight

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

5. Study Description

Brief Summary
Esophageal cancer is one of the major diseases that seriously threatens an individual's health and life. To reduce the incidence of postoperative complications and mortality of esophageal cancer, thoraco-laparoscopic oesophagectomy (TLE) has been recommended by many guidelines since the 2000s. Additionally, with developments in endoscopy technology in recent years, mediastinoscopy-assisted transhiatal esophagectomy (MATHE) has been used in clinical practice. In 2015, the first mediastinoscopy combined with laparoscopic radical esophagectomy was reported systematically by Hitoshi Fujiwara. This surgical procedure has been performed in many centres in China. However, there is no multicentre prospective randomized controlled study that explored the safety, feasibility and short-term clinical efficacy between mediastinoscopy-assisted transhiatal esophagectomy and thoraco-laparoscopic esophagectomy. We aim to evaluate the feasibility and safety of MATHE.
Detailed Description
Esophageal resection remains the mainstay of treatment for esophageal cancer patients. Despite improvements in surgical technique and perioperative management, esophagectomy carries considerable operative risk. To reduce the incidence of postoperative complications and mortality of esophageal cancer, the optional of minimally invasive esophagectomy has been recommended by many guidelines since 2000s. In addition, with the development of endoscopy technology in recent years, mediastinoscopy-assisted transhiatal esophagectomy (MATHE) has been used in clinical practices. In 2015, the first mediastinoscopy combined with laparoscopic radical esophagectomy was reported systematically by Hitoshi Fujiwara. This surgical procedure has been performed in many centers of China since then. Compared with MIE, MATHE allows controlled dissection of upper mediastinum and biopsy of mediastinal lymph nodes. No study directly comparing MATHE versus MIE has been reported to date. In this report, we compare MATHE with MIE in terms of surgical feasibility, safety, and survival.We intend to adopt a randomized controlled study method. The study group is mediastinoscopy-assisted transhiatal esophagectomy (MATHE) group, and the control group is thoraco-laparoscopic esophagectomy (TLE) group. This study is expected to provide high-level evidence for the new methods and to provide better treatment options for patients with esophageal cancer.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Neoplasms
Keywords
Mediastinoscopy-assisted transhiatal esophagectomy (MATHE), Thoraco-laparoscopic esophagectomy (TLE)

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
160 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Thoraco-laparoscopic esophagectomy
Arm Type
Active Comparator
Arm Description
Treated by thoraco-laparoscopic esophagectomy in the centers with enough experience in esophageal resection and the volume ≧80 cases each year.
Arm Title
Mediastinoscopy-assisted transhiatal esophagectomy
Arm Type
Active Comparator
Arm Description
Treated by mediastinoscopy-assisted transhiatal esophagectomy in the centers with enough experience in esophageal resection and the volume ≧80 cases each year.
Intervention Type
Procedure
Intervention Name(s)
Thoraco-laparoscopic esophagectomy
Intervention Description
Thoraco-laparoscopic esophagectomy surgery
Intervention Type
Procedure
Intervention Name(s)
Mediastinoscopy-assisted transhiatal esophagectomy
Intervention Description
Mediastinoscopy-assisted transhiatal esophagectomy surgery
Primary Outcome Measure Information:
Title
Postoperative respiratory complications
Description
These respiratory complications involve respiratory distress or failure after the operation with continuation of mechanical ventilation, pulmonary atelectasis requiring sputum suction by bronchoscopy, pneumonia requiring specific antibiotics confirmed by thoracic X-ray or CT scan of the thorax and a positive sputum culture, and acute respiratory distress syndrome.
Time Frame
30 days after surgery
Secondary Outcome Measure Information:
Title
pulmonary function indicators
Description
pulmonary function indicators
Time Frame
30 days after surgery
Title
anastomotic fistula
Description
anastomotic fistula
Time Frame
30 days after surgery
Title
recurrent laryngeal nerve palsy
Description
recurrent laryngeal nerve palsy
Time Frame
recurrent laryngeal nerve palsy
Title
DFS
Description
Disease-free survival,DFS
Time Frame
3 years
Title
duration of surgery
Description
Total operation time
Time Frame
Intraoperation
Title
Blood loss
Description
blood loss during the surgery
Time Frame
Intraoperation
Title
Conversion rate
Description
conversion to thoracotomy during surgery
Time Frame
Intraoperation
Title
postoperative hospital stay
Description
postoperative hospital stay
Time Frame
postoperation
Title
postoperative pain score
Description
postoperative pain score
Time Frame
postoperation
Title
drainage time
Description
drainage time
Time Frame
postoperation
Title
R0 resection rate
Description
R0 resection rate
Time Frame
Intraoperation
Title
Lymph node dissection
Description
During the surgery, lymph node dissection were performed. The number of removed lymph-nodes were recorded according to the postoperative pathological diagnosis, and the stations of the lymph node were recorded.
Time Frame
Intraoperation
Title
Local recurrence
Description
three-year local tumour recurrence or distant metastasis rate after surgery
Time Frame
3 years
Title
30-day mortality after surgery
Description
30-day mortality after surgery
Time Frame
postoperation

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years≤age≤ 80 years; Histologically diagnosed with squamous cell carcinoma by endoscopic biopsy, cT1-3N0M0; Primary tumour is located in the thoracic oesophagus No clinical evidence of distant organ metastasis No severe comorbidity, can tolerate anesthesia; ECOG PS scores≤2; The patients sign informed consents by themselves. Exclusion Criteria: Cervical or abdominal oesophageal carcinoma; Previous oesophagectomy, gastrectomy, or mediastinal surgery; Current uncontrolled illness such as severe cardiac disease, uncontrollable hypertension or diabetes, or active bacterial infection; Unable to tolerate tracheal intubation and general anaesthesia as determined by an anaesthesiologist preoperatively; Pregnant or lactating women; ECOG PS scores>2; Considered unsuitable, such as those who do not agree to participate in the trial.
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Juwei Mu, MD
Phone
8610-87788495
Ext
7140
Email
mujuwei@cicams.ac.cn
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Juwei Mu, MD
Organizational Affiliation
National Cancer Center of China
Official's Role
Principal Investigator
Facility Information:
Facility Name
Cancer Hospital of Chinese Academy of Medical Sciences Shenzhen Center
City
Shenzhen
State/Province
Guangdong
ZIP/Postal Code
518000
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Juwei Mu, MD

12. IPD Sharing Statement

Plan to Share IPD
No

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Mediastinoscopy-assisted Transhiatal Esophagectomy Versus Thoraco-laparoscopic Esophagectomy for Esophageal Cancer

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