Predictors of Progression in Barrett's Esophagus: Current Knowledge and Future Directions

被引:80
作者
Prasad, Ganapathy A. [1 ]
Bansal, Ajay [2 ,3 ]
Sharma, Prateek [2 ,3 ]
Wang, Kenneth K. [1 ]
机构
[1] Mayo Clin, Barretts Esophagus Unit, Div Gastroenterol & Hepatol, Rochester, MN USA
[2] Vet Affairs Med Ctr, Div Gastroenterol, Kansas City, MO USA
[3] Univ Kansas, Sch Med, Kansas City, MO USA
基金
美国国家卫生研究院;
关键词
LOW-GRADE DYSPLASIA; IN-SITU HYBRIDIZATION; GASTROESOPHAGEAL-REFLUX DISEASE; CELL-CYCLE ABNORMALITIES; PROTON PUMP INHIBITORS; BODY-MASS INDEX; NEOPLASTIC PROGRESSION; RISK-FACTORS; ANTIREFLUX SURGERY; FLOW-CYTOMETRY;
D O I
10.1038/ajg.2010.2
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Barrett's esophagus (BE) is the strongest risk factor for esophageal adenocarcinoma (EAC), a malignancy with persistently poor long-term outcomes. EAC is thought to develop through progression of metaplasia to dysplasia to invasive carcinoma. Identification of factors predicting progression to EAC would help in focusing surveillance, chemoprevention, or ablation for those deemed to be at highest risk of progression. We performed a comprehensive review of the literature and summarized current evidence on risk factors for progression in subjects with known BE. Clinical and demographic factors (age, male gender, length of BE segment) are associated with modestly increased odds of progression to EAC in some studies. Biomarkers such as aneuploidy and p53 loss of heterozygosity have been associated with increased risk of progression to high-grade dysplasia and/or EAC in single-center prospective cohort studies. Promising newer techniques and markers have been recently reported with the potential to help risk stratify BE subjects. Development of a comprehensive BE risk progression score comprised of both clinical and biomarker variables should be the ultimate goal and can be achieved by multicenter prospective collaborative efforts. Although it would be challenging, creation of such a score has the potential to improve outcomes and make the management of patients with BE more cost-effective.
引用
收藏
页码:1490 / 1502
页数:13
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