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巴雷特食管的光动力疗法:17例患者的治疗结果

Photodynamic therapy in Barrett's esophagus: results of treatment of 17 patients.

作者信息

Weiss Alan A, Wiesinger Holly A R, Owen David

机构信息

British Columbia Cancer Agency, Vancouver, British Columbia V5Z 4E6.

出版信息

Can J Gastroenterol. 2006 Apr;20(4):261-4. doi: 10.1155/2006/954153.

DOI:10.1155/2006/954153
PMID:16609754
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2659902/
Abstract

BACKGROUND

Barrett's esophagus (BE) with dysplasia may progress to esophageal adenocarcinoma. Photodynamic therapy is a promising treatment for BE.

OBJECTIVE

To determine if photodynamic therapy is an acceptable alternative to esophagectomy in BE patients with high-grade dysplasia or early adenocarcinoma.

METHODS

Seventeen patients were treated with photodynamic therapy for BE and high-grade dysplasia or early esophageal adenocarcinoma. Patients with residual Barrett's epithelium were treated with supplemental argon plasma coagulation or potassium titanyl phosphate laser. Patients underwent follow-up endoscopy three, six, nine and 12 months post-treatment, then every six to 12 months. Mean follow-up was 21 months.

RESULTS

High-grade dysplasia or early adenocarcinoma was completely eliminated in nine of 15 (60%) patients. High-grade dysplasia was downgraded in one patient, persisted in one patient and progressed in four patients. Two patients with early esophageal adenocarcinoma were nonresponders. Complications included stricture, sunburn, urticaria, small pleural effusions, esophageal spasm and transient atrial fibrillation.

CONCLUSIONS

Photodynamic therapy with supplemental ablation is a good, noninvasive therapy for elimination of high-grade dysplasia and early adenocarcinoma in BE. Failure to eliminate dysplastic epithelium occurred in 40% of the patients, thereby necessitating careful follow-up.

摘要

背景

伴有发育异常的巴雷特食管(BE)可能进展为食管腺癌。光动力疗法是一种有前景的BE治疗方法。

目的

确定光动力疗法对于伴有高级别发育异常或早期腺癌的BE患者是否是食管切除术的可接受替代方案。

方法

17例伴有高级别发育异常或早期食管腺癌的BE患者接受了光动力治疗。残留巴雷特上皮的患者接受了补充氩等离子体凝固或磷酸钛钾激光治疗。患者在治疗后3、6、9和12个月接受随访内镜检查,然后每6至12个月检查一次。平均随访时间为21个月。

结果

15例患者中有9例(60%)的高级别发育异常或早期腺癌被完全消除。1例患者的高级别发育异常降级,1例患者持续存在,4例患者进展。2例早期食管腺癌患者无反应。并发症包括狭窄、晒伤、荨麻疹、少量胸腔积液、食管痉挛和短暂性心房颤动。

结论

补充消融的光动力疗法是消除BE中高级别发育异常和早期腺癌的一种良好的非侵入性治疗方法。40%的患者未能消除发育异常上皮,因此需要仔细随访。

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本文引用的文献

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Photodynamic therapy in Barrett's esophagus.
Gastrointest Endosc Clin N Am. 2003 Jul;13(3):483-9, vii. doi: 10.1016/s1052-5157(03)00049-7.
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Biomarkers in Barrett's esophagus.巴雷特食管中的生物标志物。
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Photodynamic therapy for Barrett's esophagus with dysplasia and/or early stage carcinoma: long-term results.光动力疗法治疗不典型增生和/或早期癌的巴雷特食管:长期结果
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Barrett's esophagus and esophageal adenocarcinoma: pathogenesis, diagnosis, and therapy.巴雷特食管与食管腺癌:发病机制、诊断及治疗
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Photodynamic therapy for dysplastic Barrett esophagus and early esophageal adenocarcinoma.发育异常的巴雷特食管和早期食管腺癌的光动力疗法
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Updated guidelines for the diagnosis, surveillance, and therapy of Barrett's esophagus.巴雷特食管诊断、监测及治疗的更新指南。
Am J Gastroenterol. 2002 Aug;97(8):1888-95. doi: 10.1111/j.1572-0241.2002.05910.x.
7
Predictors of progression in Barrett's esophagus II: baseline 17p (p53) loss of heterozygosity identifies a patient subset at increased risk for neoplastic progression.巴雷特食管进展的预测因素II:基线17p(p53)杂合性缺失可识别肿瘤进展风险增加的患者亚组。
Am J Gastroenterol. 2001 Oct;96(10):2839-48. doi: 10.1111/j.1572-0241.2001.04236.x.
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Long-term nonsurgical management of Barrett's esophagus with high-grade dysplasia.巴雷特食管伴高级别异型增生的长期非手术治疗
Gastroenterology. 2001 Jun;120(7):1607-19. doi: 10.1053/gast.2001.25065.
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Persistent genetic abnormalities in Barrett's esophagus after photodynamic therapy.光动力治疗后巴雷特食管的持续性基因异常
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Predictors of progression to cancer in Barrett's esophagus: baseline histology and flow cytometry identify low- and high-risk patient subsets.巴雷特食管进展为癌症的预测因素:基线组织学和流式细胞术可识别低风险和高风险患者亚组。
Am J Gastroenterol. 2000 Jul;95(7):1669-76. doi: 10.1111/j.1572-0241.2000.02196.x.