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Neoplastic Barrett Esophagus: Endoscopic Piecemeal vs. En Bloc Resection

Not Applicable
Recruiting
Conditions
Barrett Esophagus
Esophagus Neoplasm
Barrett Adenocarcinoma
Interventions
Procedure: Endoscopic mucosal resection
Procedure: Endoscopic submucosal dissection
Registration Number
NCT03427346
Lead Sponsor
Universitätsklinikum Hamburg-Eppendorf
Brief Summary

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.

Detailed Description

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.

Recruitment & Eligibility

Status
RECRUITING
Sex
All
Target Recruitment
407
Inclusion Criteria
  • patients to be treated for Barrett's esophagus by mucosal resection and following ablative therapy
  • Barrett's mucosal extension up to 10 cm maximum.
  • patient's ability for compliance to therapy
  • signed Informed Consent
Exclusion Criteria
  • any lesion questionable to be resectable by mucosectomy, e.g. bulky lesions ≥10 mm in endoscopy und endosonography, suspected deep submucosal infiltration, ulcers, suspected or by FNA confirmed lymph node infiltration
  • Barrett's esophagus > 10 cm
  • lesions that would afford resection of more than 2/3rd of esophagal circumference
  • two or more single Barrett's lesions with bulky HGIN or early cancer histology, not to be resectable in one half of esophageal circumference
  • planned circumferencial resections
  • very serious general illness and metastatic carcinoma
  • coagulation disorder or anticoagulants that make biopsies and resections impossible
  • American Society of Anesthesiologists (ASA) status > III
  • pregnancy and lactation
  • remainders or recurrences after therapeutic history of Barrett's espohagus

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
EMREndoscopic mucosal resectionEndoscopic mucosal resection
ESDEndoscopic submucosal dissectionEndoscopic submucosal dissection
Primary Outcome Measures
NameTimeMethod
Eradication rate of neoplastic Barrett's Esophagus, initial therapy success9 months after end of therapy (resection and ablation)

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

Eradication rate of neoplastic Barrett's Esophagus33 months after end of therapy (resection and ablation)

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

Secondary Outcome Measures
NameTimeMethod
Surveillance of Barrett's mucosa after incomplete resections and recurrences51 months

follow up of all cases with initially incomplete EMR or ESD resections as well as recurrences after resection and ablation

conclusions of Tumor Board in case of re resection and outcome if postitive cancer histology51 months

any Treatment and follow up in case of positive cancer histology

Determination of differences in Barrett's esophagus subtypes: patterns3 months

patterns of Barrett's mucosa, e,g, Kudo Classification

ESD success of resection2 days

rate of en bloc and R0 resections among the initially by ESD resected tissues

Eradication rate of complete Barrett's Esophagus, initial therapy success9 months after end of treatment (resection and ablation)

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

Recurrence rate of neoplastic Barrett's Esophagus, initial therapy success9 months after end of therapy (resection and ablation)

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.

freedom of recurrence rate of complete Barrett's Esophagus, initial therapy success9 months after end of treatment (resection and ablation)

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

EMR success of resection9 months after end of treatment (resection and ablation)

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.

Determination of differences in Barrett's esophagus subtypes: size3 months

size of Barrett's mucosa, e.g. Prague Classification

Determination of differences in Barrett's esophagus subtypes: form3 months

form of Barrett's mucosa

Eradication rate of complete Barrett's Esophagus, freedom of recurrence33 months after end of treatment (resection and ablation)

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

Determination of differences in Barrett's esophagus subtypes: histologies3 months

histological assessment of Barrett's mucosa

Intervention time18 months

time requested for each resection and ablative sessions

Trial Locations

Locations (2)

Orlando Health

🇺🇸

Orlando, Florida, United States

University Medical Center Hamburg-Eppendorf

🇩🇪

Hamburg, Germany

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