Endoscopic photodynamic therapy (PDT) is undertaken only when tumour is visible endoscopically with malignancy biopsy confirmed. Patients will be either Group A: inoperable cases with locally advanced cancer when the aim is palliation of dysphagia, or Group E: patients with early stage I-II disease who are unsuitable for surgery or decline operation, when the intent is curative. Following assessment for suitability for PDT and counselling, Photofrin 2 mg/(kg bw) is administered 24-72 h before endoscopic illumination using a Diode 630 nm laser. Illumination may be either interstitial or intraluminal at a dose of 100-200J/cm. (C) 2006 Elsevier B.V. All rights reserved.
引用
收藏
页码:93 / 95
页数:3
相关论文
共 4 条
[1]
Hudson Emma J., 1994, Proceedings of the SPIE - The International Society for Optical Engineering, V2371, P563, DOI 10.1117/12.203416