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使用铱-192对无法手术切除的胆管癌进行内镜治疗。

Endoscopic management of inoperable cholangiocarcinoma using iridium-192.

作者信息

Ede R J, Williams S J, Hatfield A R, McIntyre S, Mair G

机构信息

Department of Gastroenterology, London Hospital, Whitechapel, UK.

出版信息

Br J Surg. 1989 Aug;76(8):867-9. doi: 10.1002/bjs.1800760834.

Abstract

We report a well tolerated endoscopic technique of administering intraluminal radiotherapy to 14 patients with inoperable cholangiocarcinoma, in which the iridium-192 wire source was inserted down a nasobiliary catheter placed within a previously inserted endoscopic biliary prosthesis, thus allowing bile flow to continue during treatment. Radiotherapy was commenced 2 weeks after biliary decompression, when the median serum bilirubin level had fallen from 213 to 34 mumol/l. A total radiation dose of 6000 cGy at 0.5 cm from the source was administered over a median of 85 h (range 77-116 h). In four patients there was a transient increase in serum bilirubin during iridium treatment and, in two cases (14 per cent), this was associated with mild cholangitis. Both cases resolved rapidly once the iridium wire and nasobiliary catheter were removed. The median hospital stay after treatment was 2.5 days (range 0-28 days). The late complications associated with stent blockage were minimized by routinely changing stents at 4-6 monthly intervals; ten of the patients have so far undergone from one to five (median three) stent changes. Five patients have died at 3.6-8.2 months (median 4.8 months) following iridium treatment; four had extensive type III hilar lesions at diagnosis. Nine patients are still alive at 5.4-31.0 months (median 16.4 months). The overall median survival after iridium therapy is 10.5 months. This technique of endoscopic biliary decompression before internal iridium administration minimizes complications by allowing biliary drainage during treatment. The role of this treatment in patients with inoperable cholangiocarcinoma awaits the results of randomized, controlled trials.

摘要

我们报告了一种耐受性良好的内镜技术,用于对14例无法手术的胆管癌患者进行腔内放射治疗。该技术是将铱 - 192线状源通过置于先前插入的内镜胆管支架内的鼻胆管导管插入,从而在治疗期间使胆汁能够持续流动。在胆管减压2周后开始放疗,此时血清胆红素中位数水平已从213降至34μmol / l。在距源0.5 cm处给予的总辐射剂量为6000 cGy,中位时间为85小时(范围77 - 116小时)。4例患者在铱治疗期间血清胆红素短暂升高,其中2例(14%)伴有轻度胆管炎。一旦移除铱丝和鼻胆管导管,这两例均迅速缓解。治疗后的中位住院时间为2.5天(范围0 - 28天)。通过每4 - 6个月定期更换支架,将与支架堵塞相关的晚期并发症降至最低;到目前为止,10例患者已进行了1至5次(中位3次)支架更换。5例患者在铱治疗后3.6 - 8.2个月(中位4.8个月)死亡;4例在诊断时患有广泛的III型肝门部病变。9例患者在5.4 - 31.0个月(中位16.4个月)仍存活。铱治疗后的总体中位生存期为10.5个月。这种在腔内给予铱之前进行内镜胆管减压的技术,通过在治疗期间允许胆汁引流,将并发症降至最低。这种治疗方法在无法手术的胆管癌患者中的作用有待随机对照试验的结果。

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