The study will compare EMR versus ESD technique (both combined with subsequent ablative therapy) of mucosal resection in Barrett's esophagus with regard to efficacy and risk in a long term setting.
For Barrett's Esophagus neoplasia of at least LGIN up to early adenocarcinoma, the aim is to debulk or completely treat polypoid dysplastic or malignant lesions in Barrett's esophagus. The Endoscopic Mucosal Resection EMR has been established to be a less invasive, safe, and effective nonsurgical therapy. The most commonly employed modalities of EMR include snare resection with and without prior submucosal injection of fluid, and resection using a cap. Since resection of larger areas can only be done piece - by- piece this kind or resection is also called piecemeal resection or piecemeal EMR. Meanwhile, another endoscopic resection has been developed called Endoscopic Submucosal Dissection ESD.It enables complete resection of neoplasms that were impossible to resect en bloc by EMR. After circumferential cutting of the surrounding mucosa of the lesion, fluid is injected into the submucosa to elevate the lesion from the muscle layer, and subsequently the connective tissue beneath the lesion is dissected. As a basic principle on histopathological and oncological terms, the en bloc resection is to be preferred since resection integrity can be evaluated much more securely. However, complexity of this kind of resection technique as well as complication rates can be different and sometimes higher than with EMR. Current approach treating Barrett's esophagus is to eradicate both neoplastic as well as pre neoplastic or non neoplastic Barrett mucosa in order to lower the relapse risk. Current treatment standard is to combine resection of visible neoplastic areas with subsequent thermo-ablation such as RFA or APC, so this approach will also be the basis of the present study. Since RFA has the largest volume of data screened it shall be the preferred method of ablation in this study.In total, data situation ist inconsistent. Short- and Long term of EMR is excellent in centres(Pech et al, Gastroenterology 2014) whereas ESD achieved only suboptimal outcomes in tree minor western studies (Neuhaus et al. Endoscopy 2012, Höbel et al., Surg Endosc 2015, Chevaux et al. Endoscopy 2015). One randomised study published in 2016 (Terheggen et al. Gut 2016) had a higher rate of R0 resections with ESD on 40 patients but no difference in complete remissions in combination with RFA. Although, this study was not empowered sufficientliy, and also showed a higher complication rate on ESD . At present no randomised study data are availale to allow statements about long term developments, so we will set up this current randomised study. We will compare data with regard to efficacy (histological completeness and relapse rates), as well as risks, e.g. perforations and strictures or stenosis by scarring.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Enrollment
407
Endoscopic resection is carried out using a double-channel scope. The lesion borders are marked with a coagulator. Saline liquid and sometimes epinephrine are injected into the submucosal layer to swell the area containing the lesion and elucidate the markings. The resected mucosa is lifted, then trapped and strangulated with a snare, and subsequently resected by electrocautery. Another method of EMR employs the use of a clear cap and prelooped snare inside the cap. After insertion, the cap is placed on the lesion and the mucosa containing the lesion is drawn up inside the cap by aspiration. The mucosa is caught by the snare and strangulated, and finally resected by electrocautery.
After circumferential cutting of the surrounding mucosa of the lesion, fluid is injected into the submucosa to elevate the lesion from the muscle layer, and the connective tissue of the submucosa beneath the lesion is dissected subsequently.
Orlando Health
Orlando, Florida, United States
RECRUITINGUniversity Medical Center Hamburg-Eppendorf
Hamburg, Germany
RECRUITINGEradication rate of neoplastic Barrett's Esophagus, initial therapy success
Rate of complete and curative eradication, free of recurrence of neoplastic Barrett's Esophagus. Endoscopical diagnostic and negative histologies for any kind of neoplasia, measured in follow up control EGD 3 months after end of treatment
Time frame: 3 months after end of therapy (resection and ablation)
Eradication rate of neoplastic Barrett's Esophagus, initial therapy success
Rate of complete and curative eradication, free of recurrence of neoplastic Barrett's Esophagus. Endoscopical diagnostic and negative histologies for any kind of neoplasia, measured in follow up control EGD 9 months after end of treatment
Time frame: 9 months after end of therapy (resection and ablation)
Eradication rate of neoplastic Barrett's Esophagus
Rate of complete and curative eradication, free of recurrence of neoplastic Barrett's Esophagus. Endoscopical diagnostic and negative histologies for any kind of neoplasia, measured in follow up control 24 months after end of treatment
Time frame: 24 months after end of therapy (resection and ablation)
Eradication rate of neoplastic Barrett's Esophagus
Rate of complete and curative eradication, free of recurrence of neoplastic Barrett's Esophagus. Endoscopical diagnostic and negative histologies for any kind of neoplasia, measured in follow up control EGD 33 months after end of treatment
Time frame: 33 months after end of therapy (resection and ablation)
Eradication rate of complete Barrett's Esophagus, initial therapy success
Rate of complete and curative eradication, free of recurrence of neoplastic and non-neoplastic Barrett's Esophagus. Endoscopical diagnostics and negative histologies for any kind of neoplasia and Barrett's metaplasia measured in follow up control EGD 3 months after end of treatment
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Time frame: 3 months after end of treatment (resection and ablation)
Eradication rate of complete Barrett's Esophagus, initial therapy success
Rate of complete and curative eradication, free of recurrence of neoplastic and non-neoplastic Barrett's Esophagus. Endoscopical diagnostics and negative histologies for any kind of neoplasia and Barrett's metaplasia measured in follow up control EGD 9 months after end of treatment
Time frame: 9 months after end of treatment (resection and ablation)
Eradication rate of complete Barrett's Esophagus, freedom of recurrence
Rate of complete and curative eradication, free of recurrence of neoplastic and non-neoplastic Barrett's Esophagus. Endoscopical diagnostics and negative histologies for any kind of neoplasia and Barrett's metaplasia measured in follow up control EGD 24 months after end of treatment
Time frame: 24 months after end of treatment (resection and ablation)
Eradication rate of complete Barrett's Esophagus, freedom of recurrence
Rate of complete and curative eradication, free of recurrence of neoplastic and non-neoplastic Barrett's Esophagus. Endoscopical diagnostics and negative histologies for any kind of neoplasia and Barrett's metaplasia measured in follow up control EGD 33 months after end of treatment
Time frame: 33 months after end of treatment (resection and ablation)
Recurrence rate of neoplastic Barrett's Esophagus, initial therapy success
rate of complete and curative eradication of neoplastic Barrett's Esophagus measured in follow up control EGD 3 months, Endoscopical diagnostic and negative histologies for any kind of neoplasia.
Time frame: 3 months after end of therapy (resection and ablation)
Recurrence rate of neoplastic Barrett's Esophagus, initial therapy success
rate of complete and curative eradication of neoplastic Barrett's Esophagus measured in follow up control EGD 9 months , Endoscopical diagnostic and negative histologies for any kind of neoplasia.
Time frame: 9 months after end of therapy (resection and ablation)
freedom of recurrence rate of complete Barrett's Esophagus, initial therapy success
Freedom of recurrence rate of neoplastic and non-neoplastic Barrett's Esophagus. Endoscopical diagnostics and negative histologies for any kind of neoplasia and Barrett's metaplasia measured in follow up control EGD 9 months (initial therapy success) after end of treatment
Time frame: 9 months after end of treatment (resection and ablation)
ESD success of resection
rate of en bloc and R0 resections among the initially by ESD resected tissues
Time frame: 2 days
EMR success of resection
Since with EMR resection success can only be measured for the depth of base initially, the second control EGD with negative histology has been chosen for Gold standard indication for resection success. After 2 negative bioptic controls a piecemeal resection of early carcinoma is classified as complete.
Time frame: 9 months after end of treatment (resection and ablation)
Surveillance of Barrett's mucosa after incomplete resections and recurrences
follow up of all cases with initially incomplete EMR or ESD resections as well as recurrences after resection and ablation
Time frame: 51 months
conclusions of Tumor Board in case of re resection and outcome if postitive cancer histology
any Treatment and follow up in case of positive cancer histology
Time frame: 51 months
Determination of differences in Barrett's esophagus subtypes: size
size of Barrett's mucosa, e.g. Prague Classification
Time frame: 3 months
Determination of differences in Barrett's esophagus subtypes: form
form of Barrett's mucosa
Time frame: 3 months
Determination of differences in Barrett's esophagus subtypes: patterns
patterns of Barrett's mucosa, e,g, Kudo Classification
Time frame: 3 months
Determination of differences in Barrett's esophagus subtypes: histologies
histological assessment of Barrett's mucosa
Time frame: 3 months
Intervention time
time requested for each resection and ablative sessions
Time frame: 18 months