Autofluorescence endoscopy in surveillance of Barrett's esophagus:: a multicenter randomized trial on diagnostic efficacy

被引:57
作者
Borovicka, J. [1 ]
Fischer, J.
Neuweiler, J.
Netzer, P.
Gschossmann, J.
Ehmann, T.
Bauerfeind, P.
Dorta, G.
Zuercher, U.
Binek, J.
Meyenberger, C.
机构
[1] Cantonal Hosp, Dept Internal Med, Div Gastroenterol Hepatol, CH-9007 St Gallen, Switzerland
[2] Univ Heidelberg, Mannheim Med Sch, Dept Publ Hlth Social & Prevent Med, D-6900 Heidelberg, Germany
[3] Inst Pathol, St Gallen, Switzerland
[4] Univ Hosp Bern, Div Gastroenterol, CH-3010 Bern, Switzerland
[5] Univ Lausanne Hosp, Div Gastroenterol, Lausanne, Switzerland
[6] Univ Zurich Hosp, Div Gastroenterol, Zurich, Switzerland
关键词
D O I
10.1055/s-2006-944726
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background and study aims: The reference surveillance method in patients with Barrett's esophagus is careful endoscopic observation, with targeted as well as random four-quadrant biopsies. Autofluorescence endoscopy (AFE) may make it easier to locate neoplasia. The aim of this study was to elucidate the diagnostic accuracy of surveillance with AFE-guided plus four-quadrant biopsies in comparison with the conventional approach. Patients and methods: A total of 187 of 200 consecutive Barrett's esophagus patients who were initially enrolled (73 % male, mean age 67 years, mean Barrett's segment length 4.6 cm), who underwent endoscopy for Barrett's esophagus in four study centers, were randomly assigned to undergo either AFE-targeted biopsy followed by four-quadrant biopsies or conventional endoscopic surveillance, also including four-quadrant biopsies (study phase 1). After exclusion of patients with early cancer or high-grade dysplasia, who underwent endoscopic or surgical treatment, as well as those who declined to participate in phase 2 of the study, 130 patients remained. These patients were examined again with the alternative method after a mean of 10 weeks, using the same methods described. The main study parameter was the detection of early cancer/adenocarcinoma or high-grade dysplasia (HGD), comparing both approaches in study phase 1: the secondary study aim in phase 2 was to assess the additional value of the AFE-guided approach after conventional surveillance, and vice versa. Test accuracy measures were derived from study phase 1. Results: In study phase 1, the AFE and conventional approaches yielded adenocarcinoma/HGD rates of 12% and 5.3%, respectively, on a per-patient basis. With AFE, four previously unrecognized adenocarcinoma/HGD lesions were identified (4.3% of the patients); with the conventional approach, one new lesion (1.1%) was identified. Of the 19 adenocarcinoma/HGD lesions detected during AFE endoscopy in study phase 1, eight were visualized, while 11 were only detected using untargeted four-quadrant biopsies (sensitivity 42%). Of the 766 biopsies classified at histology as being nonneoplastic, 58 appeared suspicious (specificity 92%, positive predictive value 12%, negative predictive value 98.5%). In study phase 2, AFE detected two further lesions in addition to the initial alternative approach in 3.2% of cases, in comparison with one lesion with conventional endoscopy (1.7%). Conclusions: In this referral Barrett's esophagus population with a higher prevalence of neoplastic lesions, the AFE-guided approach improved the diagnostic yield for neoplasia in comparison with the conventional approach using four-quadrant biopsies. However, AFE alone was not suitable for replacing the standard four-quadrant biopsy protocol.
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页码:867 / 872
页数:6
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