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激光和低剂量率近距离放射治疗对恶性气道梗阻的管理:梅奥诊所的经验

Management of malignant airway compromise with laser and low dose rate brachytherapy. The Mayo Clinic experience.

作者信息

Schray M F, McDougall J C, Martinez A, Cortese D A, Brutinel W M

机构信息

Division of Radiation Oncology, Mayo Clinic, Rochester, Minnesota 55905.

出版信息

Chest. 1988 Feb;93(2):264-9. doi: 10.1378/chest.93.2.264.

Abstract

Between January 1983 and October 1985, 65 patients with malignant airway compromise have had 93 flexible bronchoscopic placements of a nylon afterloading catheter for low dose rate iridium-192 temporary intraluminal brachytherapy. All patients received prior (59 patients) and/or concurrent (13 patients) external beam irradiation to "tolerance" and were not candidates for surgery. Forty of these patients also received neodymium-YAG laser treatment prior to brachytherapy in a planned combined approach to provide immediate symptomatic relief and facilitate catheter placement. A dose of 3,000 cGy is prescribed to 5 mm and 10 mm radii over 20-40 hours in the bronchus and trachea, respectively. Of 59 patients treated with palliative intent, 40 patients (68 percent) have had follow-up bronchoscopy, 18 patients have had clinical follow-up only, and one patient was lost to follow-up. Of 40 patients examined by bronchoscope in follow-up, 24 (60 percent) responded, eight were stable, and eight progressed. Lack of progression after prior external beam radiation for periods of greater than 12 months, six-12 months and less than six months yielded response rates to brachytherapy in 83 percent, 50 percent and 31 percent, respectively. Most patients with clinical follow-up only expired at early intervals with airway palliation from extra-airway disease progression. Four of five patients treated with curative intent are disease-free at a median of 16 months. Eleven patients have experienced fistula and/or hemorrhage, of which seven instances (11 percent of all patients) appear to be treatment-induced. This brachytherapy technique is simple, well tolerated, and convenient for the patient providing airway palliation in the significant majority of patients with acceptable risk.

摘要

1983年1月至1985年10月期间,65例恶性气道狭窄患者接受了93次尼龙后装导管的可弯曲支气管镜置入术,用于低剂量率铱-192腔内临时近距离放疗。所有患者均接受过先前(59例)和/或同期(13例)的外照射,剂量达“耐受量”,均不适合手术治疗。其中40例患者在近距离放疗前还接受了钕钇铝石榴石激光治疗,采用计划性联合治疗方案以立即缓解症状并便于导管置入。分别在支气管和气管内20 - 40小时内,给予5毫米和10毫米半径处3000厘戈瑞的剂量。59例以姑息治疗为目的的患者中,40例(68%)接受了随访支气管镜检查,18例仅接受了临床随访,1例失访。随访中接受支气管镜检查的40例患者中,24例(60%)有反应,8例病情稳定,8例进展。先前外照射后无进展时间大于12个月、6 - 12个月和小于6个月的患者,近距离放疗的有效率分别为83%、50%和31%。大多数仅接受临床随访的患者早期因气道外疾病进展导致气道姑息治疗无效而死亡。5例以根治为目的治疗的患者中,4例在中位时间16个月时无疾病复发。11例患者出现瘘管和/或出血,其中7例(占所有患者的11%)似乎是治疗引起的。这种近距离放疗技术简单,耐受性良好,对患者方便,能为绝大多数风险可接受的患者提供气道姑息治疗。

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