ESTD vs. VATS for Upper Gastrointestinal Submucosal Tumors

Sponsor
Nanfang Hospital of Southern Medical University (Other)
Overall Status
Unknown status
CT.gov ID
NCT01768104
Collaborator
(none)
200
1
2
24
8.3

Study Details

Study Description

Brief Summary

The purpose of this study is to determine the efficacy and safety of endoscopic submucosal tunnel dissection (ESTD) compared with video-assisted thoracoscopic surgery (VATS) in the treatment of upper gastrointestinal submucosal tumors.

Condition or Disease Intervention/Treatment Phase
  • Procedure: ESTD
  • Procedure: VATS
N/A

Detailed Description

Most upper gastrointestinal submucosal tumors (SMTs), especially the gastrointestinal stromal tumors (GISTs) and leiomyoma, are regarded as benign if they are less than 3cm in size. Thus, it has been suggested that patients should receive periodic endoscopic follow-up in case of gradual changes in size; however this can be stressful and troublesome for patients. Nevertheless, some of these tumors do have a malignant potential, and management by periodic endoscopic surveillance may lead to delayed diagnosis of malignancy. Therefore, it is necessary to remove the SMTs.

To date, several approaches have been used for the treatment of upper gastrointestinal SMTs, including open, thoracoscopic and laparoscopic surgery, and endoscopic approaches such as band ligation, endoscopic submucosal dissection (ESD), and endoscopic full-thickness resection (EFR). However, the surgical approaches are invasive with a longer hospital stay and greater cost, while the endoscopic approaches were limited by technical difficulty, incomplete resections and risk of perforation.

Recently, the technique of peroral endoscopic myotomy (POEM) for esophageal achalasia was introduced, a procedure in which a submucosal tunnel is created to expose and dissect the circular muscle of the esophagus. Inspired by the POEM approach, we have successfully used a similar method, endoscopic submucosal tunnel dissection (ESTD), to resect SMTs in upper gastrointestinal.

However, the long-term efficacy and safety of ESTD were not determined, and there was no prospective study compared the ESTD with other conventional approaches. Therefore, we plan to conduct this prospective randomized controlled trial, aim to determine the efficacy and safety of ESTD, compared with the pneumatic dilation, in the treatment of upper gastrointestinal SMTs originating from the muscularis propria layer .

Study Design

Study Type:
Interventional
Anticipated Enrollment :
200 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
None (Open Label)
Primary Purpose:
Treatment
Official Title:
Endoscopic Submucosal Tunnel Dissection Versus Video-assisted Thoracoscopic Surgery for Upper Gastrointestinal Submucosal Tumors: a Prospective Randomized Controlled Trial
Study Start Date :
Dec 1, 2011
Anticipated Primary Completion Date :
Dec 1, 2013
Anticipated Study Completion Date :
Dec 1, 2013

Arms and Interventions

Arm Intervention/Treatment
Experimental: ESTD

Endoscopic submucosal tunnel dissection (ESTD) for patients with upper gastrointestinal submucosal tumors (SMTs)

Procedure: ESTD
A 2-cm longitudinal mucosal incision was made, approximately 5cm proximal to the submucosal tumor (SMTs). Submucosal dissection was done, creating a submucosal tunnel until the tumor was visible. Dissection was done along the margin of the tumor. After the tumor had been removed, the potential bleeding area in the tunnel was coagulated. Endoclips were used to close the entry of the submucosal tunnel. (Gong W et al. ESTD for upper gastrointestinal submucosal tumors… Endoscopy 2012; 44: 231-235)
Other Names:
  • Endoscopic submucosal tunnel dissection (ESTD)
  • Submucosal tunneling endoscopic resection (STER)
  • Submucosal endoscopic tumor resection (SET)
  • Active Comparator: VATS

    Video-assisted thoracoscopic surgery (VATS) for patients with upper gastrointestinal submucosal tumors (SMTs)

    Procedure: VATS
    General anesthesia with double lumen intubation. Three to four cameras or working ports are placed over the chest wall. After the lesion is visualized by thoracoscopy, the mediastinal pleura over the tumor is incised longitudinally by an endoscopic hook electrocauterizer. The mass is exposed after the overlying muscle is split longitudinally. The retracting suture is placed over the mass and then meticulously dissect the plane between the mass and the submucosal layer. The integrity of the mucosa must be checked. The muscle layer is re-approximated and a chest tube is place through one of the ports. (Luh et al. World Journal of Surgical Oncology 2012, 10:52)
    Other Names:
  • Video-assisted thoracoscopic surgery
  • Video-thoracoscopic enucleation
  • Outcome Measures

    Primary Outcome Measures

    1. En bloc resection [During the operation]

      The En bloc resection was defined as a one-piece resection of the entire lesion without fragmentation

    Secondary Outcome Measures

    1. Curative resection [From date of randomization until the date of pathological diagnosis, an expected average of 7 days]

      The curative resection was defined as the resected specimen with vertical and lateral margins free of neoplasia in pathological diagnosis.

    2. Procedure related complication [From date of operation until the occurrence of the procedure related complication, which most occur within 7 days after operation, assessed up to 2 years]

      Perforation, Delayed bleeding, Pneumothorax, Subcutaneous emphysema, Anastomotic leak, etc.

    3. Short-term morbidity [From date of randomization until the date of death from any cause, assessed up to 3 months]

      Any cause death

    4. Local recurrence [From date of randomization until the follow-up ended, assessed up to 2 years]

      Local recurrence was defined as endoscopic or histological diagnosis of cancer at the resected site in follow-up

    5. Quality of life [From date of randomization until the follow-up ended, assessed up to 2 years]

      Patients will complete the quality-of-life questionnaires (the Medical Outcomes Study 36-Item Short-Form Health Survey, SF-36) for assessing quality of life

    Eligibility Criteria

    Criteria

    Ages Eligible for Study:
    15 Years to 75 Years
    Sexes Eligible for Study:
    All
    Accepts Healthy Volunteers:
    No
    Inclusion Criteria:
    • Between 18 and 75 years of age

    • Patient with upper gastrointestinal submucosal tumor

    • Signed informed consent

    Exclusion Criteria:
    • Severe cardio-pulmonary disease or other serious disease leading to unacceptable surgical risk

    • Endoscopic ultrasound (EUS) or CT signs of metastasis

    • Mega-oesophagus (greater than 7 cm) or Oesophageal diverticula in the distal oesophagus

    • Previous oesophageal or gastric surgery

    • Pregnancy or lactation women, or ready to pregnant women

    • Not capable of filling out questionnaires

    Contacts and Locations

    Locations

    Site City State Country Postal Code
    1 Nanfang Hospital of Southern Medical University Guangzhou Guangdong China 510515

    Sponsors and Collaborators

    • Nanfang Hospital of Southern Medical University

    Investigators

    • Principal Investigator: Wei Gong, M.D., Department of Gastroenterology, Nanfang Hospital of Southern Medical University

    Study Documents (Full-Text)

    None provided.

    More Information

    Additional Information:

    Publications

    Responsible Party:
    Nanfang Hospital of Southern Medical University
    ClinicalTrials.gov Identifier:
    NCT01768104
    Other Study ID Numbers:
    • NFEK-201211-K1
    • 201120
    First Posted:
    Jan 15, 2013
    Last Update Posted:
    Jan 15, 2013
    Last Verified:
    Dec 1, 2011

    Study Results

    No Results Posted as of Jan 15, 2013