内镜超声和PDT诊断胰腺癌

J. DeWitt
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引用次数: 0

摘要

背景和目的:在一项单中心、前瞻性、剂量递增的1期研究中,treatment-naïve局部晚期胰腺癌(LAPC)患者接受静脉注射聚硫脲钠,2天后进行EUS-PDT。EUS-PDT采用19号针穿刺,插入1.0 cm光漫射器,630 nm光照射。PDT后18天进行CT扫描以评估胰腺坏死的变化。CT后7天开始使用nab -紫杉醇和吉西他滨。结果:12例患者(平均年龄67±6岁;在头部和/或颈部(8例)或身体和/或尾部(4例)有肿瘤(平均直径45.2±12.9 mm)的患者(8例男性)接受EUS-PDT。与基线成像相比,12例患者中有6例(50%)在EUS-PDT后观察到肿瘤坏死体积和百分比增加。PDT未发生严重不良事件。结论:EUS-PDT在技术上是可行的。II期研究是必要的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Endoscopic ultrasound and PDT for pancreatic cancer
Background and Aims: In a single-center, prospective, dose-escalation phase 1 study, patients with treatment-naïve locally advanced pancreatic cancer (LAPC) received intravenous porfimer sodium followed 2 days later by EUS-PDT. EUS-PDT was performed by puncture with a 19-gauge needle and insertion of a 1.0-cm light diffuser and illumination with a 630-nm light. A CT scan 18 days after PDT was done to assess for change in pancreatic necrosis. Nab-paclitaxel and gemcitabine were initiated 7 days after CT. Results: Twelve patients (mean age, 67 ± 6 years; 8 male) with tumors (mean diameter, 45.2 ± 12.9 mm) in the head and/or neck (8) or body and/or tail (4) underwent EUS-PDT. Compared with baseline imaging, increased volume and percentage of tumor necrosis were observed in 6 of 12 patients (50%) after EUS-PDT. No serious adverse events from PDT occurred. Conclusion: EUS-PDT for LAPC is technically feasible. Phase II studies are warranted.
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