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Submucosal Tumor Removal by Endoscopic Excision Therapy (STREET)

Primary Purpose

Submucosal Tumor of Stomach

Status
Recruiting
Phase
Not Applicable
Locations
Germany
Study Type
Interventional
Intervention
removal of submucosal gastric tumor preferably by Full Thickness Resection Device (FTRD)
Sponsored by
Universitätsklinikum Hamburg-Eppendorf
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Submucosal Tumor of Stomach focused on measuring Submucosal Tumor of Stomach, GIST, FTRD

Eligibility Criteria

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

Inclusion Criteria:

  • Patients with endoscopically diagnosed and endosonographically confirmed submucosal tumors of 0.5 to 2 cm in the stomach without definitive histology / cytology
  • Initial diagnosis less than 2 years ago
  • No contraindication to endoscopic resection
  • Patient's informed consent

Exclusion Criteria:

  • Tumor size > 2 cm
  • Tumors with proven / suspected malignancy for which oncologically no endoscopic resection should be performed, i.e. for which oncological or surgical therapy is planned
  • SMT known > 2 Years
  • Patients with severe general illnesses (limited operability) or malignancies
  • Clotting disorders
  • Pregnancy

Sites / Locations

  • University Hospital FreiburgRecruiting
  • University Hospital Hamburg EppendorfRecruiting
  • University Hospital MarburgRecruiting

Arms of the Study

Arm 1

Arm Type

Other

Arm Label

Removal of submucosal gastric tumor preferably by Full Thickness Resection Device (FTRD)

Arm Description

FTRD (Ovesco company) in tumors up to 10 mm and predominantly intraluminal growth directly by sucking into the cap, at 10-20 mm and/or intramural/extramural growth by prior circumcision and lateral preparation, so that the lesions can be better pulled into the cap. The procedure depends on the endosonographic extent of the findings. The lesions are pulled into the cap with grippers and other instruments and, if necessary, with a snare and then resected with FTRD

Outcomes

Primary Outcome Measures

Rate of GIST tumors
Rate of GIST tumors in a preferably unselected patient cohort of small submucous gastric tumors in which histology is not known

Secondary Outcome Measures

Technical success
Technical success rate (R0/R1 resection) of the chosen resection technique
Complication rate
Complication rate of the chosen resection technique
influencing factors on the GIST rate: tumor size
Influence of tumor size on the GIST rate
Influencing factors on the GIST rate: position of tumor
Influence of tumor position in the stomach
Influencing factors on the GIST rate: endoscopic ultrasound image
endoscopic ultrasound image with pattern and position in the wall
Influencing factors on the GIST rate: patient's age
Age of patients
Influencing factors on the GIST rate: patient's gender
gender of patients
Influencing factors on the GIST rate: anamnesis
anamnesis including initial diagnosis
Patient's preferred approach
Patient preferences for removal (consent rate for the study) versus follow-up
data for cost-benefit calculation
Establishment of a date base for a cost-benefit calculation comparing follow-up vs. removal

Full Information

First Posted
January 23, 2021
Last Updated
July 1, 2023
Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
Ovesco Endoscopy AG
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1. Study Identification

Unique Protocol Identification Number
NCT04913077
Brief Title
Submucosal Tumor Removal by Endoscopic Excision Therapy
Acronym
STREET
Official Title
Prospective One-armed Observational Study of Full-thickness Resection of Small Hypoechoic Submucosal Gastric Tumors (≤2 cm)
Study Type
Interventional

2. Study Status

Record Verification Date
July 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 10, 2020 (Actual)
Primary Completion Date
November 2024 (Anticipated)
Study Completion Date
February 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Universitätsklinikum Hamburg-Eppendorf
Collaborators
Ovesco Endoscopy AG

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
Smaller submucosal tumors (SMT) in the stomach are usually seen as an incidental finding during a gastroscopy, although current diagnostics usually do not clearly indicate what type of tumor it is. In summary, there is no good evidence for dealing with SMT. In this study, an endoscopic full-thickness resection, primarily with the FTRD device, is to be offered to all patients with gastric SMT without a confirmed histology seen in a certain period of time . Patients who do not want to take advantage of this are included in a systematic follow-up program. The investigators hope to learn about the rate of so-called GIST tumors and other histologies, as well as the rate of change in the follow-up group. Also, study contents will be accuracy of endosonographic imaging and puncture in comparison with resection histology, technical feasibility and histological completeness of the FTRD- based endoscopic (full-wall) resection option, complications of such a resection (secondary bleeding and dehiscences), and patient preferences with standardized information.
Detailed Description
Smaller submucous tumors in the stomach are usually seen as a random finding in gastroscopies and present a diagnostic dilemma to the doctor and patient: type specification is usually unclear whether it is an absolutely benign (without degeneration potential) or a malignant or prone tumor (usually gastrointestinal stromal tumor, GIST). However, this is crucial for further management. In endosonographic imaging there are only approximate values in the differential diagnosis between GIST and non-GIST, the endoscopic biopsy is too superficial, and the hit rate of endosonographic pin puncture is limited, and in most studies is less than 70% Therefore, one can only make assumptions and create a risk profile from imaging and tumor size (limit size 3 cm, partly also 2 cm). Both follow-up recommendations (rather no GIST) and laparoscopic surgical removal (proven or probable/possible GIST) are not rarely without clear preference, especially for smaller tumors. For these indications, a simple endoscopic removal option comparable to the polypectomy in the colon (where no histological type diagnosis is made before) does not exist. Previous studies are usually subject to bias in several directions: The frequency of GIST tumors among submucous tumors/lesions (SMT) in the stomach is unclear. Gastroenterological series always contain smaller GIST tumors, but are reported almost exclusively from clinics. The rate of these tumors in the overall collective of patients seen in the field of (mostly established) gastroenterologists is thus completely unclear. Surgical or oncological series have usually included more aggressive tumors consisting mainly or exclusively of GIST tumors, therefore do not allow epidemiological conclusions. If no surgery is performed (and thus a definitive histology is forced), only information from follow-up examinations remains. Previous follow-up studies show the dilemma of insufficient differential diagnosis of lesions by endosonography and (endosonographic or other) biopsy, which usually have insufficient accuracy. In addition, the follow-up time in the studies hardly extends beyond 2 years. The "gastroenterological gut instinct" that these small lesions are not dangerous may be true, but is not proven.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Submucosal Tumor of Stomach
Keywords
Submucosal Tumor of Stomach, GIST, FTRD

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Model Description
Submucosal gastric Tumors up to 2 centimeters of size
Masking
None (Open Label)
Allocation
N/A
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Removal of submucosal gastric tumor preferably by Full Thickness Resection Device (FTRD)
Arm Type
Other
Arm Description
FTRD (Ovesco company) in tumors up to 10 mm and predominantly intraluminal growth directly by sucking into the cap, at 10-20 mm and/or intramural/extramural growth by prior circumcision and lateral preparation, so that the lesions can be better pulled into the cap. The procedure depends on the endosonographic extent of the findings. The lesions are pulled into the cap with grippers and other instruments and, if necessary, with a snare and then resected with FTRD
Intervention Type
Other
Intervention Name(s)
removal of submucosal gastric tumor preferably by Full Thickness Resection Device (FTRD)
Other Intervention Name(s)
Endoscopic submucosal dissection (ESD)
Intervention Description
FTRD (Ovesco company) in tumors up to 10 mm and predominantly intraluminal growth directly by sucking into the cap, at 10-20 mm and/or intramural/extramural growth by prior circumcision and lateral preparation, so that the lesions can be better pulled into the cap. The procedure depends on the endosonographic extent of the findings. The lesions are pulled into the cap with grippers and other instruments and, if necessary, with a snare and then resected with FTRD
Primary Outcome Measure Information:
Title
Rate of GIST tumors
Description
Rate of GIST tumors in a preferably unselected patient cohort of small submucous gastric tumors in which histology is not known
Time Frame
through study completion, approximately 2 years
Secondary Outcome Measure Information:
Title
Technical success
Description
Technical success rate (R0/R1 resection) of the chosen resection technique
Time Frame
through study completion, approximately 2 years
Title
Complication rate
Description
Complication rate of the chosen resection technique
Time Frame
through study completion, approximately 2 years
Title
influencing factors on the GIST rate: tumor size
Description
Influence of tumor size on the GIST rate
Time Frame
through study completion, approximately 2 years
Title
Influencing factors on the GIST rate: position of tumor
Description
Influence of tumor position in the stomach
Time Frame
through study completion, approximately 2 years
Title
Influencing factors on the GIST rate: endoscopic ultrasound image
Description
endoscopic ultrasound image with pattern and position in the wall
Time Frame
through study completion, approximately 2 years
Title
Influencing factors on the GIST rate: patient's age
Description
Age of patients
Time Frame
through study completion, approximately 2 years
Title
Influencing factors on the GIST rate: patient's gender
Description
gender of patients
Time Frame
through study completion, approximately 2 years
Title
Influencing factors on the GIST rate: anamnesis
Description
anamnesis including initial diagnosis
Time Frame
through study completion, approximately 2 years
Title
Patient's preferred approach
Description
Patient preferences for removal (consent rate for the study) versus follow-up
Time Frame
through study completion, approximately 2 years
Title
data for cost-benefit calculation
Description
Establishment of a date base for a cost-benefit calculation comparing follow-up vs. removal
Time Frame
through study completion, approximately 2 years

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: Patients with endoscopically diagnosed and endosonographically confirmed submucosal tumors of 0.5 to 2 cm in the stomach without definitive histology / cytology Initial diagnosis less than 2 years ago No contraindication to endoscopic resection Patient's informed consent Exclusion Criteria: Tumor size > 2 cm Tumors with proven / suspected malignancy for which oncologically no endoscopic resection should be performed, i.e. for which oncological or surgical therapy is planned SMT known > 2 Years Patients with severe general illnesses (limited operability) or malignancies Clotting disorders Pregnancy
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Thomas Rösch, Prof. Dr.
Phone
+49 40 7410
Ext
50098
Email
t.roesch@uke.de
First Name & Middle Initial & Last Name or Official Title & Degree
Guido Schachschal, PD Dr.
Phone
+49 40 7410
Ext
50097
Email
g.schachschal@uke.de
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Thomas Rösch, Prof. Dr.
Organizational Affiliation
Universitätsklinikum Hamburg-Eppendorf
Official's Role
Principal Investigator
Facility Information:
Facility Name
University Hospital Freiburg
City
Freiburg
ZIP/Postal Code
79106
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Arthur R Schmidt, Prof. Dr.
Email
arthur.schmidt@uniklinik-freiburg.de
First Name & Middle Initial & Last Name & Degree
Arthur R Schmidt, Prof. Dr.
Facility Name
University Hospital Hamburg Eppendorf
City
Hamburg
ZIP/Postal Code
20246
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Thomas Rösch, Prof. Dr.
Phone
+49 40 7410
Ext
50098
Email
t.roesch@uke.de
First Name & Middle Initial & Last Name & Degree
Guido Schachschal, PD Dr.
Phone
+49 49 7410
Ext
50097
Email
g.schachschal@uke.de
First Name & Middle Initial & Last Name & Degree
Thomas Rösch, Prof. Dr.
First Name & Middle Initial & Last Name & Degree
Guido Schachschal, PD Dr.
First Name & Middle Initial & Last Name & Degree
Lennika Calavrezos, Dr.
First Name & Middle Initial & Last Name & Degree
Katharina Zimmermann-Fraedrich, Dr.
First Name & Middle Initial & Last Name & Degree
Philip Dautel, Dr.
Facility Name
University Hospital Marburg
City
Marburg
ZIP/Postal Code
35039
Country
Germany
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ulrike W Denzer, Prof. Dr.
Email
uwdenzer@gmail.com
First Name & Middle Initial & Last Name & Degree
Ulrike W Denzer, Prof. Dr.

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
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29658639
Citation
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Submucosal Tumor Removal by Endoscopic Excision Therapy

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