The Case for Endoscopic Treatment of Non-dysplastic and Low-Grade Dysplastic Barrett's Esophagus

被引:55
|
作者
Fleischer, David E. [15 ]
Odze, Robert [14 ]
Overholt, Bergein F. [13 ]
Carroll, John [12 ]
Chang, Kenneth J. [11 ]
Das, Ananya [15 ]
Goldblum, John [10 ]
Miller, Daniel [9 ]
Lightdale, Charles J. [8 ]
Peters, Jeffrey [7 ]
Rothstein, Richard [6 ]
Sharma, Virender K. [5 ]
Smith, Daniel [4 ]
Velanovich, Victor [3 ]
Wolfsen, Herbert [2 ]
Triadafilopoulos, George [1 ]
机构
[1] Stanford Univ, Sch Med, Div Gastroenterol & Hepatol, Stanford, CA 94305 USA
[2] Mayo Clin Florida, Dept Internal Med, Jacksonville, FL 32224 USA
[3] Henry Ford Hosp, Dept Surg, Detroit, MI 48202 USA
[4] Mayo Clin Florida, Dept Surg, Jacksonville, FL 32224 USA
[5] Az Ctr Digest Hlth, Gilbert, AZ 85297 USA
[6] Dartmouth Hitchcock Med Ctr, Dept Internal Med, Lebanon, NH 03756 USA
[7] Univ Rochester, Dept Surg, Rochester, NY 14642 USA
[8] Columbia Presbyterian Med Ctr, Dept Internal Med, New York, NY 10032 USA
[9] Emory Univ, Med Ctr, Dept Surg, Atlanta, GA 30322 USA
[10] Cleveland Clin Fdn, Dept Pathol, Cleveland, OH 44195 USA
[11] Univ Calif Irvine, Orange, CA 92868 USA
[12] Georgetown Univ, Dept Internal Med, Washington, DC 20007 USA
[13] Gastrointestinal Associates, Knoxville, TN 37909 USA
[14] Brigham & Womens Hosp, Dept Pathol, Boston, MA 02115 USA
[15] Mayo Clin Arizona, Dept Internal Med, Scottsdale, AZ 85259 USA
关键词
Barrett's esophagus; Radiofrequency ablation; Esophageal cancer; Adenocarcinoma; Intestinal metaplasia; Low-grade dysplasia; COLUMNAR-LINED ESOPHAGUS; LAPAROSCOPIC NISSEN FUNDOPLICATION; GASTROESOPHAGEAL-REFLUX DISEASE; COST-UTILITY ANALYSIS; RADIOFREQUENCY ABLATION; NEOPLASTIC PROGRESSION; PHOTODYNAMIC THERAPY; INTESTINAL METAPLASIA; COLORECTAL-CANCER; CLONAL EXPANSION;
D O I
10.1007/s10620-010-1218-1
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Non-dysplastic mucosa (ND-) in Barrett's esophagus (BE) shows clonal molecular aberrations, loss of cell cycle control, and other features of "neoplasia." These changes occur prior to morphologic expression of neoplasia (dysplasia). Morphologic evaluation of dysplasia is fraught with error, and, as a result, often leads to false-negative and false-positive diagnoses. Early "crypt dysplasia" is difficult to detect, and is often missed in routine biopsy specimens. Some studies show substantial progression rates of low-grade dysplasia (LGD), and crypt dysplasia, to esophageal adenocarcinoma (EAC). Dysplasia, even when fully developed, may, in certain circumstances, be difficult to differentiate from non-dysplastic (regenerating) BE. Radiofrequency ablation (RFA) is a safe and effective method for removing mucosa at risk of cancer. Given the difficulties of dysplasia assessment in mucosal biopsies, and the molecular characteristics of ND-BE, this technique should be considered for treatment of all BE patients, including those with ND or LGD. Post-ablation neo-squamous epithelium reveals no molecular abnormalities, and is biologically stable. Given that prospective randomized controlled trials of ablative therapy for ND-BE aiming at reducing EAC incidence and mortality are unlikely to be completed in the near future, endoscopic ablation is a valid management option. The success of RFA in achieving safe, uniform, reliable, and predictable elimination of BE allows surgeons to combine fundoplication with RFA. Currently, there is no type of treatment for dysplastic or non-dysplastic BE that achieves a complete response in 100% of patients, eliminates all risk of developing cancer, results in zero adverse events, is less expensive in terms of absolute costs than surveillance, is durable for 20+ years, or eliminates the need for surveillance. Regardless, RFA shows established safety, efficacy, durability, and cost-effective profiles that should be considered in the management of patients with non-dysplastic or low-grade dysplastic BE.
引用
收藏
页码:1918 / 1931
页数:14
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