Objective: This study reviews the development of Barrett's esophagus in patients with gastroesophageal reflux disease. Here we evaluate the progression of the disorder into esophageal adenocarcinoma in patients with Barrett's esophagus under treatment, and the effectiveness of current medical or surgical therapy regarding mucosal regression or progression. Methods: A MEDLINE search was performed to analyze data published in English between 1980 and 2002. Results: Despite successful surgery, Barrett's esophagus developed in 5.8-18.9% of patients with gastroesophageal reflux disease. The rate was higher in patients receiving medical therapy (11.1-33.8%). In long-term follow-up studies the mucosal changes (length of Barrett's mucosa, histological malformations) were reported to progress in 13.8-40.7% of patients after medical therapy and in 3.4-15.3% after surgical intervention. The risk of developing esophageal carcinoma on grounds of Barrett's esophagus was 1.3-4.6 and 0-8.1% in patients receiving medical and surgical treatment, respectively. In the published studies, the rate of complete regression of Barrett's esophagus following surgery varied between 0 and 26.4%. Discussion: Long-term follow-up studies confirm the histological progression in Barrett's esophagus. Therefore, the current medical or surgical therapies do not prevent malignant transformation of the columnar epithelial lining of the esophagus. However, their combination may delay progression and cancer formation.
机构:
CHU Cochin Port Royal, AP HP, Serv Gastroenterol, F-75014 Paris, France
Univ Paris 05, Fac Med, F-75270 Paris 06, FranceCHU Cochin Port Royal, AP HP, Serv Gastroenterol, F-75014 Paris, France
Leblanc, Sarah
Pommaret, Elise
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CHU Cochin Port Royal, AP HP, Serv Gastroenterol, F-75014 Paris, France
Univ Paris 05, Fac Med, F-75270 Paris 06, FranceCHU Cochin Port Royal, AP HP, Serv Gastroenterol, F-75014 Paris, France
Pommaret, Elise
Coriat, Romain
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CHU Cochin Port Royal, AP HP, Serv Gastroenterol, F-75014 Paris, France
Univ Paris 05, Fac Med, F-75270 Paris 06, FranceCHU Cochin Port Royal, AP HP, Serv Gastroenterol, F-75014 Paris, France
Coriat, Romain
Prat, Frederic
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CHU Cochin Port Royal, AP HP, Serv Gastroenterol, F-75014 Paris, France
Univ Paris 05, Fac Med, F-75270 Paris 06, FranceCHU Cochin Port Royal, AP HP, Serv Gastroenterol, F-75014 Paris, France
机构:
Univ Texas Dallas, Southwestern Med Sch, VA North Texas Hlth Care Syst, Dept Med, Dallas, TX USA
Univ Texas Dallas, Southwestern Med Ctr, Harold C Simmons Comprehens Canc Ctr, Dallas, TX USAUniv Texas Dallas, Southwestern Med Sch, VA North Texas Hlth Care Syst, Dept Med, Dallas, TX USA
机构:
Hutchison MRC Res Ctr, MRC Canc Cell Unit, Cambridge CB2 0XZ, EnglandHutchison MRC Res Ctr, MRC Canc Cell Unit, Cambridge CB2 0XZ, England
Bird-Lieberman, Elizabeth L.
Fitzgerald, Rebecca C.
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Hutchison MRC Res Ctr, MRC Canc Cell Unit, Cambridge CB2 0XZ, England
Addenbrookes Hosp, Cambridge CB2 2QQ, EnglandHutchison MRC Res Ctr, MRC Canc Cell Unit, Cambridge CB2 0XZ, England
机构:
Peter MacCallum Canc Ctr, Surg Oncol Res Lab, Div Canc Surg, Melbourne, Vic 8006, Australia
Univ Melbourne, St Vincents Hosp, Dept Surg, Melbourne, Vic, AustraliaPeter MacCallum Canc Ctr, Surg Oncol Res Lab, Div Canc Surg, Melbourne, Vic 8006, Australia
Phillips, Wayne A.
Lord, Reginald V.
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Univ New S Wales, St Vincents Ctr Appl Med Res, Sydney, NSW, AustraliaPeter MacCallum Canc Ctr, Surg Oncol Res Lab, Div Canc Surg, Melbourne, Vic 8006, Australia
Lord, Reginald V.
Nancarrow, Derek J.
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机构:Peter MacCallum Canc Ctr, Surg Oncol Res Lab, Div Canc Surg, Melbourne, Vic 8006, Australia
Nancarrow, Derek J.
Watson, David I.
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机构:
Flinders Univ S Australia, Flinders Med Ctr, Dept Surg, Adelaide, SA 5001, AustraliaPeter MacCallum Canc Ctr, Surg Oncol Res Lab, Div Canc Surg, Melbourne, Vic 8006, Australia
Watson, David I.
Whiteman, David C.
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Royal Brisbane Hosp, Canc Control Labs, Queensland Inst Med Res, Brisbane, Qld 4029, AustraliaPeter MacCallum Canc Ctr, Surg Oncol Res Lab, Div Canc Surg, Melbourne, Vic 8006, Australia