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Nucletron FIRST系统的技术评估:遥控后装近距离放射治疗种子植入系统与制造商规格及美国医学物理师协会任务组报告建议的一致性

A technical evaluation of the Nucletron FIRST system: conformance of a remote afterloading brachytherapy seed implantation system to manufacturer specifications and AAPM Task Group report recommendations.

作者信息

Rivard Mark J, Evans Dee-Ann Radford, Kay Ian

机构信息

Department of Radiation Oncology, Tufts University School of Medicine, Tufts-New England Medical Center, 750 Washington Street, Boston, Massachusetts 02111, USA.

出版信息

J Appl Clin Med Phys. 2005 Winter;6(1):22-50. doi: 10.1120/jacmp.v6i1.1985. Epub 2005 Jan 12.

Abstract

The Fully Integrated Real-time Seed Treatment (FIRST) system by Nucletron has been available in Europe since November 2001 and is being used more and more in Canada and the United States. Like the conventional transrectal ultrasound implant procedure, the FIRST system utilizes an ultrasound probe, needles, and brachytherapy seeds. However, this system is unique in that it (1) utilizes a low-dose-rate brachytherapy seed remote afterloader (the seedSelectron), (2) utilizes 3D image reconstruction acquired from electromechanically controlled, nonstepping rotation of the ultrasound probe, (3) integrates the control of a remote afterloader with electromechanical control of the ultrasound probe for integrating the clinical procedure into a single system, and (4) automates the transfer of planning information and seed delivery to improve quality assurance and radiation safety. This automated delivery system is specifically intended to address reproducibility and accuracy of seed positioning during implantation. The FIRST computer system includes two software environments: SPOT PRO and seedSelectron; both are used to facilitate treatment planning and brachytherapy seed implantation from beginning to completion of the entire procedure. In addition to these features, the system is reported to meet certain product specifications for seed delivery positioning accuracy and reproducibility, seed calibration accuracy and reliability, and brachytherapy dosimetry calculations. Consequently, a technical evaluation of the FIRST system was performed to determine adherence to manufacturer specifications and to the American Association of Physicists in Medicine (AAPM) Task Group Reports 43, 53, 56, 59, and 64 and recommendations of the American Brachytherapy Society (ABS). The United States Nuclear Regulatory Commission (NRC) has recently added Licensing Guidance for the seedSelectron system under 10 CFR 35.1000. Adherence to licensing guidance is made by referencing applicable AAPM Task Group recommendations. In general, results of this evaluation indicated that the system met its claimed specifications as well as the applicable recommendations outlined in the AAPM and ABS reports.

摘要

Nucletron公司的全集成实时种子源治疗(FIRST)系统自2001年11月起在欧洲上市,在加拿大和美国的使用也越来越多。与传统的经直肠超声植入程序一样,FIRST系统使用超声探头、针和近距离放射治疗种子源。然而,该系统的独特之处在于:(1)使用低剂量率近距离放射治疗种子源遥控后装设备(seedSelectron);(2)利用通过超声探头的机电控制非步进旋转获取的三维图像重建;(3)将遥控后装设备的控制与超声探头的机电控制集成在一起,以便将临床程序整合到一个单一系统中;(4)实现计划信息和种子源输送的自动化,以提高质量保证和辐射安全性。这种自动输送系统专门用于解决植入过程中种子源定位的可重复性和准确性问题。FIRST计算机系统包括两个软件环境:SPOT PRO和seedSelectron;两者都用于辅助从整个程序的开始到结束的治疗计划制定和近距离放射治疗种子源植入。除了这些功能外,据报道该系统还满足种子源输送定位准确性和可重复性、种子源校准准确性和可靠性以及近距离放射治疗剂量计算的某些产品规格。因此,对FIRST系统进行了技术评估,以确定其是否符合制造商的规格以及美国医学物理学家协会(AAPM)任务组报告43、53、56、59和64以及美国近距离放射治疗协会(ABS)的建议。美国核管理委员会(NRC)最近根据10 CFR 35.1000增加了对seedSelectron系统的许可指南。通过参考适用的AAPM任务组建议来遵守许可指南。总体而言,该评估结果表明,该系统符合其声称的规格以及AAPM和ABS报告中概述的适用建议。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2ebb/5723507/fa7dd6ce0a48/ACM2-6-022-g001.jpg

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