PROSpective Assessment of Post EmR Recurrence (PROSPER)
Primary Purpose
Colonic Adenoma, Colonic Polyp
Status
Completed
Phase
Not Applicable
Locations
Australia
Study Type
Interventional
Intervention
SCAR technique
Sponsored by
About this trial
This is an interventional treatment trial for Colonic Adenoma focused on measuring Colonoscopy, Endoscopic Mucosal Resection, Adenoma Recurrence, EMR defect thermal ablation
Eligibility Criteria
Inclusion Criteria:
- All laterally spreading lesions >= 20mm referred to the named tertiary referral centres
- Must consent to involvement
Exclusion Criteria:
- Histology other than specified
- Lesion involving the ileocaecal valve
- Pregnancy: currently pregnant or attempting to become pregnant
- Lactation: currently breastfeeding
- Taken clopidogrel within 7 days
- Taken warfarin within 5 days
- Had full therapeutic dose unfractionated heparin within 6 hours
- Had full therapeutic dose low molecular weight heparin (LMWH) within 12 hours
- Known clotting disorder
- Previous attempt at EMR of the polyp referred for resection
Sites / Locations
- Westmead Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
SERT 0, SCAR (low risk)
SERT 1-4, SCAR (high risk)
Arm Description
Patients with Sydney EMR Recurrence Tool (SERT scoring) score 0. These patients will be invited to return for follow up at 18 months and will have thermal ablation (SCAR technique) of the endoscopic resection defect margin.
Patients with Sydney EMR Recurrence Tool score 1-4 (SERT scoring). These patients will be invited to return for follow up at 4-6 months and will have thermal ablation (SCAR technique) of the endoscopic resection defect margin.
Outcomes
Primary Outcome Measures
Adenoma recurrence
Recurrence of adenoma at first and second surveillance colonoscopy
Secondary Outcome Measures
Need for surgery
need for surgery due to adenoma recurrence or complication
Bleeding after EMR
Pain after EMR
Delayed perforation after EMR
Full Information
NCT ID
NCT02957058
First Posted
November 3, 2016
Last Updated
June 28, 2023
Sponsor
Western Sydney Local Health District
1. Study Identification
Unique Protocol Identification Number
NCT02957058
Brief Title
PROSpective Assessment of Post EmR Recurrence
Acronym
PROSPER
Official Title
A Prospective Study Stratifying Patients to Follow up Intervals Based on Risk of Recurrence Post Wide Field Colonic EMR
Study Type
Interventional
2. Study Status
Record Verification Date
June 2023
Overall Recruitment Status
Completed
Study Start Date
January 2017 (undefined)
Primary Completion Date
January 2022 (Actual)
Study Completion Date
April 2023 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Western Sydney Local Health District
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
To prospectively validate the SERT (Sydney EMR Recurrence Tool) scoring system for adenoma recurrence rates around the endoscopic mucosal resection (EMR) scar after wide field-EMR with thermal treatment applied to the defect margin. The primary aim of the study will be to ensure the safety of this approach and there will be constant monitoring to ensure that this is the case.
Detailed Description
Colonoscopy and polypectomy reduces the anticipated incidence of colorectal malignancy in patients with significant adenomatous polyps by approximately 80% in long term follow up. Most endoscopists routinely perform removal of small polyps. However, removal of flat colonic neoplasia 20mm in size or larger is more complex and requires specific endoscopic techniques, one such technique being termed wide field endoscopic mucosal resection (WF-EMR). Traditionally these lesions were treated surgically at significant expense to the healthcare system. Endoscopic treatment of large colonic polyps reduces health care costs by approximately $11,000 per patient treated, saves bed days and avoids surgery in more than 90% of patients.
EMR describes the endoscopic technique of treating colorectal adenomatous polyps with submucosal lifting and careful piecemeal snare resection. This procedure has been shown to be safe and effective at resecting lesions limited to the mucosa. Clearly the importance of predicting lesions that are unlikely to have invaded the deeper layers is of the utmost importance here, and significant improvements in our ability to assess this have been made in large volume centres such as Westmead
An important longer-term complication of EMR of large flat colonic neoplasia is the phenomenon of residual polyp tissue or polyp recurrence, which will be the focus of the proposed research study. Recurrence is detected by surveillance colonoscopies (SC), which are performed at defined intervals after the index procedure. Our current standard for safe surveillance interval at Westmead after >= 20mm EMR is 5 months (SC1). In the largest study to date, the Australian Colonic EMR (ACE) study, recurrence at SC1 stands at 16.5% for all patients.
We have recently come to the end of a randomised trial (SCAR) of thermal treatment (snare tip soft coagulation, STSC) of the EMR defect margin (SCAR technique), with the findings to be presented at the Digestive Diseases Week in San Diego. The results of this trial (n=353) are promising with a risk of adenoma recurrence in the treated group of 6.4% vs 20.7% in the non-treated group (relative risk 0.3, p < .001). There have been no adverse events related to this treatment. The investigators plan to perform this intervention on all patients in the proposed study.
In addition, there is increasing evidence, both in the scientific literature and at our institution, that there are identifiable factors at the initial EMR that predict recurrence at SC1. Current data from the ACE cohort suggests that increasing size of lesion (>=40mm), presence of high grade dysplasia (HGD) in the resection specimen and intra-procedural bleeding requiring endoscopic control predict greater likelihood of recurrence. The investigators have created, and have submitted for publication, a risk score for recurrence after EMR known as the Sydney EMR Recurrence Tool (SERT), (figure 1). SERT was created by binomial logistic regression analysis (figure 2) on 692 patients (model cohort) from the ACE study and validated on the remaining 691 patients (validation cohort) who had undergone SC1. Kaplan Meier curves (figure 3) were used to determine the predicted incidence of recurrence at various points in time after EMR on the validation cohort (figure 4). The strength of SERT lies in predicting the absence of recurrence, with negative predictive value of 92.6% at first surveillance colonoscopy. While this score was not derived from patients treated with SCAR technique, it is expected that the stratification of lesions by SERT will continue to be valid with lower overall rates.
Crucial in ensuring the absence of polyp recurrence in the long term is surveillance colonoscopy. In the endoscopy department at Westmead the current standard of follow-up is SC1 at 5 months. This short interval is costly and inconvenient for patients, but has been thought necessary due to previous anxiety over recurrence rates.
The investigators therefore propose a study to prospectively evaluate recurrence after WF-EMR by triaging follow up based on SERT, with all lesions treated by SCAR technique. Patients with SERT 0 lesions would be triaged to first follow up at 18 months (the usual time for SC2) since their rate of recurrence until this point is predicted to be very low (8.5%) and such recurrence is likely to be easily treated endoscopically after this time (in the validation cohort recurrence was commonly diminutive (<5mm, 67%), uni-focal (75%), with no high grade dysplasia (HGD). All recurrences were treatable endoscopically. This compares favourably to the 90.3% successful endoscopic treatment of recurrence rate in a recent meta-analysis.
Higher risk lesions (SERT 1-4) would be triaged to earlier follow up at 6 then 18 months, since their predicted risk of recurrence at 6 months is 14.8% and at 18 months is 31.8%. All lesions would require a follow up procedure at approximately 36 months after the original EMR since both groups rate of recurrence increases by this time (figure 4) and this will be suggested to the referring specialist.
Risk factor Score Laterally Spreading lesion Size >= 40, score 2 Intraprocedural bleeding requiring endoscopic control, score 1 High grade dysplasia, score 1
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colonic Adenoma, Colonic Polyp
Keywords
Colonoscopy, Endoscopic Mucosal Resection, Adenoma Recurrence, EMR defect thermal ablation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
700 (Actual)
8. Arms, Groups, and Interventions
Arm Title
SERT 0, SCAR (low risk)
Arm Type
Active Comparator
Arm Description
Patients with Sydney EMR Recurrence Tool (SERT scoring) score 0. These patients will be invited to return for follow up at 18 months and will have thermal ablation (SCAR technique) of the endoscopic resection defect margin.
Arm Title
SERT 1-4, SCAR (high risk)
Arm Type
Active Comparator
Arm Description
Patients with Sydney EMR Recurrence Tool score 1-4 (SERT scoring). These patients will be invited to return for follow up at 4-6 months and will have thermal ablation (SCAR technique) of the endoscopic resection defect margin.
Intervention Type
Procedure
Intervention Name(s)
SCAR technique
Intervention Description
Thermal ablation of the EMR margin using ERBE Soft Coagulation (Effect 4, 80 watts) and the operator choice of endoscopic resection snare
Primary Outcome Measure Information:
Title
Adenoma recurrence
Description
Recurrence of adenoma at first and second surveillance colonoscopy
Time Frame
Variable dependent on SERT score
Secondary Outcome Measure Information:
Title
Need for surgery
Description
need for surgery due to adenoma recurrence or complication
Time Frame
18 months
Title
Bleeding after EMR
Time Frame
2 weeks
Title
Pain after EMR
Time Frame
2 weeks
Title
Delayed perforation after EMR
Time Frame
2 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
All laterally spreading lesions >= 20mm referred to the named tertiary referral centres
Must consent to involvement
Exclusion Criteria:
Histology other than specified
Lesion involving the ileocaecal valve
Pregnancy: currently pregnant or attempting to become pregnant
Lactation: currently breastfeeding
Taken clopidogrel within 7 days
Taken warfarin within 5 days
Had full therapeutic dose unfractionated heparin within 6 hours
Had full therapeutic dose low molecular weight heparin (LMWH) within 12 hours
Known clotting disorder
Previous attempt at EMR of the polyp referred for resection
Facility Information:
Facility Name
Westmead Hospital
City
Westmead
State/Province
New South Wales
ZIP/Postal Code
2145
Country
Australia
12. IPD Sharing Statement
Citations:
PubMed Identifier
33798525
Citation
Sidhu M, Shahidi N, Gupta S, Desomer L, Vosko S, Arnout van Hattem W, Hourigan LF, Lee EYT, Moss A, Raftopoulos S, Heitman SJ, Williams SJ, Zanati S, Tate DJ, Burgess N, Bourke MJ. Outcomes of Thermal Ablation of the Mucosal Defect Margin After Endoscopic Mucosal Resection: A Prospective, International, Multicenter Trial of 1000 Large Nonpedunculated Colorectal Polyps. Gastroenterology. 2021 Jul;161(1):163-170.e3. doi: 10.1053/j.gastro.2021.03.044. Epub 2021 Mar 31.
Results Reference
derived
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PROSpective Assessment of Post EmR Recurrence
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