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RFA to Prevent Metachronous Squamous Neoplasia Recurrence After Complete Endoscopic Submucosal Dissection

Primary Purpose

Esophageal Squamous Cell Neoplasm

Status
Recruiting
Phase
Not Applicable
Locations
Taiwan
Study Type
Interventional
Intervention
Radiofrequency ablation
Endoscopy
Lugol's Solution (1.5%)
Sponsored by
E-DA Hospital
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Esophageal Squamous Cell Neoplasm focused on measuring Early esophageal squamous cell neoplasm, Radiofrequency ablation, Endoscopic submucosal dissection, Esophageal cancer, Recurrence, Field cancerization

Eligibility Criteria

20 Years - 90 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Adults with early stage ESCNs (squamous high grade dysplasia, carcinoma in situ, or T1N0M0 SCC) who were treated by endoscopic submucosal dissection.
  • Lugol staining showed "speckled" (>10 small lugol-unstained lesions) pattern of background mucosa.

Exclusion Criteria:

  • Having a history of incomplete endoscopic treatment, or complications during/after treatment (perforation, stricture).
  • Having history of systemic chemotherapy or radiation therapy for esophagus or post esophagectomy.
  • Life expectancy <2 yr.
  • Decompensated cirrhosis (Child score B, C).
  • Having large esophageal varices.
  • Poor performance status (ECOG>2).

Sites / Locations

  • EDA HospitalRecruiting

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

No Intervention

Arm Label

RFA group

Control group

Arm Description

Balloon type RFA (12J/cm2, 1 application) will be applied for the entire speckled esophageal mucosa at the 3 months after complete ESD. Oral prednisolone 30mg/day will be prescribed at day 3 after RFA procedure and continue for 28 days to prevent the post-RFA stenosis.

No intervention; surveillance endoscopy alone

Outcomes

Primary Outcome Measures

Tumor recurrence
Metachronous tumor recurrence is defined as a tumor (high-grade dysplasia or squamous cell carcinoma) recurring at a new site after more than 6 months of complete remission status.

Secondary Outcome Measures

Major adverse events
including perforation, dysphagia, stenosis, defined as the failure of a standard endoscope (9.8 mm in diameter) to pass through the stenosis, or others resulting in the patients intolerable and discontinued intervention.

Full Information

First Posted
May 28, 2017
Last Updated
March 2, 2023
Sponsor
E-DA Hospital
Collaborators
National Taiwan University Hospital
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1. Study Identification

Unique Protocol Identification Number
NCT03183115
Brief Title
RFA to Prevent Metachronous Squamous Neoplasia Recurrence After Complete Endoscopic Submucosal Dissection
Official Title
Preemptive Radiofrequency Ablation for Esophageal Speckled Lugol Background Mucosa to Prevent Metachronous Neoplastic Recurrence After Complete Endoscopic Submucosal Dissection ~A Randomized Controlled Study
Study Type
Interventional

2. Study Status

Record Verification Date
March 2023
Overall Recruitment Status
Recruiting
Study Start Date
April 18, 2016 (Actual)
Primary Completion Date
October 30, 2025 (Anticipated)
Study Completion Date
December 30, 2026 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
E-DA Hospital
Collaborators
National Taiwan University Hospital

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 a highly lethal disease, and its incidence is still increasing in the world. Recent advances in image-enhanced techniques such as Lugol chromoendoscopy and narrow band imaging, the number of patients with early esophageal squamous cell neoplasias (ESCNs) detected has markedly increased. Endoscopic submucosal dissection (ESD) enables en bloc resection of the neoplasia, and the resected specimen allows for a pathological assessment to evaluate the curability. However, the patients who received complete ESD for early ESCNs frequently developed metachronous recurrence. The cumulative metachronous recurrence rate at 5 years was 50%, and the mean annual incidence of newly diagnosed metachronous tumors was 10%. Among them, those with "speckled" lugol staining pattern over the esophageal background mucosa have the highest risk and should be seen as a precancerous lesion of ESCCs. This issue is gaining attention in the era of endoscopic treatment, but currently there was no appropriate strategy to prevent the tumor recurrence in these high-risk subjects. Endoscopic radiofrequency ablation (RFA) is a rapidly evolving therapeutic modality, and recent studies have shown its efficacy and safety for eradicating for flat type early ESCNs. To search a best strategy for the prevention of ESCNs, the investigators thus propose a hypothesis that the preemptive RFA for esophageal "speckled" lugol background mucosa may prevent the metachronous neoplastic recurrence after complete endoscopic resection.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Esophageal Squamous Cell Neoplasm
Keywords
Early esophageal squamous cell neoplasm, Radiofrequency ablation, Endoscopic submucosal dissection, Esophageal cancer, Recurrence, Field cancerization

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
RFA group
Arm Type
Experimental
Arm Description
Balloon type RFA (12J/cm2, 1 application) will be applied for the entire speckled esophageal mucosa at the 3 months after complete ESD. Oral prednisolone 30mg/day will be prescribed at day 3 after RFA procedure and continue for 28 days to prevent the post-RFA stenosis.
Arm Title
Control group
Arm Type
No Intervention
Arm Description
No intervention; surveillance endoscopy alone
Intervention Type
Procedure
Intervention Name(s)
Radiofrequency ablation
Intervention Description
HALO360 System (Covidien GI Solutions, Sunnyvale, California, USA), which has been approved by the US Food and Drug Administration (FDA) and is approved for use in Europe (CE mark) and Taiwan (Ministry of Health and Welfare). Because the HALO 360 balloon catheter has been phased out since 2019, a new Barrx™ 360 Express catheter was used thereafter.
Intervention Type
Device
Intervention Name(s)
Endoscopy
Intervention Description
The participants will receive meticulous endoscopic examination with Lugol chromoendoscopy and Narrow-band imaging
Intervention Type
Drug
Intervention Name(s)
Lugol's Solution (1.5%)
Intervention Description
Before the RFA intervention, the participants will received Lugol staining over the esophagus
Primary Outcome Measure Information:
Title
Tumor recurrence
Description
Metachronous tumor recurrence is defined as a tumor (high-grade dysplasia or squamous cell carcinoma) recurring at a new site after more than 6 months of complete remission status.
Time Frame
From date of randomization until the date of first documented tumor recurrence, assessed up to 100 months
Secondary Outcome Measure Information:
Title
Major adverse events
Description
including perforation, dysphagia, stenosis, defined as the failure of a standard endoscope (9.8 mm in diameter) to pass through the stenosis, or others resulting in the patients intolerable and discontinued intervention.
Time Frame
From date of intervention until the date of first documented adverse events, assessed up to 12months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Adults with early stage ESCNs (squamous high grade dysplasia, carcinoma in situ, or T1N0M0 SCC) who were treated by endoscopic submucosal dissection. Lugol staining showed "speckled" (>10 small lugol-unstained lesions) pattern of background mucosa. Exclusion Criteria: Having a history of incomplete endoscopic treatment, or complications during/after treatment (perforation, stricture). Having history of systemic chemotherapy or radiation therapy for esophagus or post esophagectomy. Life expectancy <2 yr. Decompensated cirrhosis (Child score B, C). Having large esophageal varices. Poor performance status (ECOG>2).
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Wen-Lun Wang, Ph.D
Phone
886-7-6150011
Ext
251346
Email
warrengodr@gmail.com
First Name & Middle Initial & Last Name or Official Title & Degree
Ching-Tai Lee, M.D.
Phone
886-7-6150011
Ext
251205
Email
fattoo@gmail.com
Facility Information:
Facility Name
EDA Hospital
City
Kaohsiung City
ZIP/Postal Code
82445
Country
Taiwan
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Wen-Lun Wang, Ph.D
Phone
886-7-6150011
Ext
251346
Email
warrengodr@gmail.com

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
The initial outcome and the data of adverse events will be shared with other researchers, by mail, when they are available.
Citations:
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20669074
Citation
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Citation
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RFA to Prevent Metachronous Squamous Neoplasia Recurrence After Complete Endoscopic Submucosal Dissection

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