IMP 重离子癌症疗法的进展与未来发展

Qiang Li, Xinguo Liu, Zhongying Dai, Pengbo He, Yuanyuan Ma, Guosheng Shen, Xiaodong Jin, Fei Ye, Xiaogang Zheng, Ting Zhao, Hui Zhang, Zheng Li, Bingwen Zou, Yuehu Pu, Weiqiang Chen
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引用次数: 0

摘要

自 1995 年以来,中国科学院近代物理研究所(IMP)一直在开展重离子癌症治疗的基础研究,如放射生物学、医学物理学和治疗技术。根据基础研究取得的成果和放疗对重离子加速器的要求,中国科学院近代物理研究所设计并在武威建造了重离子治疗专用设备,命名为重离子医疗设备(HIMM)。HIMM 设备由两个电子回旋共振离子源(一个回旋加速器作为注入器,一个同步加速器作为主加速器)和四个不同的治疗室组成,治疗室配备了被动或主动束流传输系统,可将碳离子加速到 400 MeV/u。在国家医疗器械检测中心对该中心进行性能检测后,又进行了细胞和动物放射生物学实验等临床前试验,并利用人体模型进行了剂量学验证,以阐明该中心提供的碳离子束的生物物理特性。根据中国医疗器械管理条例,在 HIMM 设备上开展了一项临床试验,招募了 46 名肿瘤患者,并有两家医院参与,旨在评估医疗器械的治疗安全性和短期疗效。临床试验的成功帮助 HIMM 设备获得了中国政府颁发的三类医疗器械证书。本文对上述各个方面进行了介绍和讨论,并对未来的改进提出了建议。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Progress in heavy ion cancer therapy at IMP and future development

Progress in heavy ion cancer therapy at IMP and future development

Basic research on heavy ion cancer therapy such as radiobiology, medical physics, and therapeutic technique has been conducted at the Institute of Modern Physics (IMP), Chinese Academy of Sciences since 1995. Based on the achievements acquired in the basic research and the requirements for a heavy ion accelerator for radiotherapy purposes, a dedicated heavy ion therapy facility named Heavy Ion Medical Machine (HIMM) was designed at IMP and constructed in Wuwei, China. The HIMM facility consists of two electron cyclotron resonance ion sources, one cyclotron as the injector and one synchrotron as the main accelerator, and four different treatment rooms equipped with passive or active beam delivery systems, and accelerates carbon ions up to 400 MeV/u. After the performance inspection of HIMM organized by the National Medical Device Inspection Center, preclinical tests like cell and animal radiobiological experiments and dosimetric verification using anthropomorphic phantoms for elucidating the biophysical properties of the carbon ion beams provided by HIMM were carried out. According to the Chinese medical device regulations, a clinical trial in which 46 tumor patients were recruited and two hospitals participated was conducted in the HIMM facility, aiming at evaluating the treatment safety and short-term efficacy of the medical device. The success of the clinical trial helped the HIMM facility be authorized by the Chinese government as a class III medical device. In this paper, all the aspects mentioned above are introduced and discussed, and implications for future improvements are also given.

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