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超声内镜引导下立体定向放疗时使用标志物的可行性:使用与标准 22G 针兼容的标志物时。

Fiducial placement for stereotactic radiation by using EUS: feasibility when using a marker compatible with a standard 22-gauge needle.

机构信息

Division of Gastroenterology, Department of Medicine, Alvin J. Siteman Cancer Center, Washington University School of Medicine, St. Louis, Missouri, USA.

出版信息

Gastrointest Endosc. 2010 Mar;71(3):630-3. doi: 10.1016/j.gie.2009.11.023.

Abstract

BACKGROUND

Stereotactic radiation by using fiducial markers permits higher doses of radiation while reducing the exposure of uninvolved, adjacent structures. EUS has been used to deploy fiducials, although a 19-gauge needle has traditionally been required.

OBJECTIVE

To report a new technique and the feasibility of deploying a fiducial compatible with a 22-gauge needle under EUS guidance.

DESIGN

Single-center, case series.

SETTING

Tertiary care referral center.

PATIENTS

Thirteen patients with primary or metastatic cancer referred for stereotactic radiation.

INTERVENTIONS

EUS-guided placement of a single fiducial marker that is compatible with a 22-gauge EUS-FNA needle.

MAIN OUTCOME MEASUREMENTS

Technical success and complications.

RESULTS

Thirteen patients referred for EUS-guided placement of a fiducial marker were identified in the endoscopic database. Targeted lesions measured 27 +/- 13 mm (range 8-50) x 21 +/- 10 mm (range 6-42). All fiducials were successfully deployed, 9 using a transgastric and 4 using a transduodenal approach. There were no EUS-associated complications. Two patients did not proceed to radiation therapy as a result of interval peritoneal metastasis. However, all fiducials were visible on the roentogram. Eleven of 13 patients (85%) required placement of 1 fiducial, whereas 2 patients (15%) required 2 fiducials.

LIMITATIONS

Uncontrolled feasibility study with limited sample size and follow-up.

CONCLUSION

EUS-guided placement of a fiducial using a 22-gauge needle is technically feasible and may permit greater access compared with the 19-gauge needle technique.

摘要

背景

使用基准标记进行立体定向放射治疗可以在减少未受累相邻结构暴露的同时提高放射剂量。EUS 已被用于部署基准标记,尽管传统上需要使用 19 号针。

目的

报告一种新的技术,即在 EUS 引导下部署与 22 号针兼容的基准标记的可行性。

设计

单中心、病例系列。

设置

三级转诊中心。

患者

13 名患有原发性或转移性癌症的患者,需要进行立体定向放射治疗。

干预措施

EUS 引导下放置单个与 22 号 EUS-FNA 针兼容的基准标记。

主要观察指标

技术成功率和并发症。

结果

在内镜数据库中确定了 13 名接受 EUS 引导下放置基准标记的患者。目标病变大小为 27 ± 13 mm(范围 8-50)x 21 ± 10 mm(范围 6-42)。所有基准标记均成功放置,9 个采用经胃途径,4 个采用经十二指肠途径。没有 EUS 相关并发症。由于间隔期腹膜转移,有 2 名患者未进行放射治疗。然而,所有基准标记均在 X 光片上可见。13 名患者中有 11 名(85%)需要放置 1 个基准标记,而 2 名患者(15%)需要放置 2 个基准标记。

局限性

未控制的可行性研究,样本量有限且随访时间短。

结论

EUS 引导下使用 22 号针放置基准标记在技术上是可行的,与 19 号针技术相比可能具有更大的可及性。

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