{"title":"Design and in-silico evaluation of a novel beamline for precision small animal pencil beam scanning delivery at clinical proton therapy facilities.","authors":"Neeraj Kurichiyanil, Marco Pinto, Katia Parodi","doi":"10.1088/1361-6560/adea08","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Preclinical small animal proton beam irradiation systems are increasingly in demand. However, the absence of dedicated systems comparable in precision to those in clinical settings presents a considerable hurdle to investigations in this field. To address this need, the SIRMIO project has developed a novel compact beam transport system configured to degrade and focus clinical proton beams. The beamline, about 1 meter long, housed in an environment to minimize scatter, includes degraders, collimators, and a permanent magnet quadrupole triplet to focus protons degraded from clinical energies. It is tailored to transport focused proton beams within the energy range of 20 to 50 MeV, ideal for small animal preclinical studies. The flexibility of this beamline design allows achieving beam-spot sizes of 1 mm sigma at the isocenter for all focused energies, with the particle fluence and spot sizes being variable through dynamic adjustment of the
collimator and magnetic lattice. 3-D scanning of the target volume is possible due to lateral beam scanning integrated into this design, without the use of additional scanning dipole magnets. 
Approach: The beamline was optimized using an accelerator beam optics code, followed by a Monte Carlo model to account for beam-matter interactions. Using an experimentally validated clinical proton beam phase space as input, degraded beams are transported through the Monte Carlo model. Outcomes are assessed for beam characteristics and dosimetric properties Main Results: Beams transported by our proposed beamline design are shown to result in dosimetric properties suitable for preclinical studies, while also emulating realistic clinically relevant beam delivery scenarios like pencil beam scanning. Compared to a similar-sized collimator-only beamline, this design
enhances transmission and reduces secondary dose at the target due to absence of scattering elements nearby.
Significance: The portable SIRMIO beamline offers a flexible, precise alternative to passive methods for adapting clinical proton beams for small animal irradiation, enhancing preclinical research with clinically relevant beam delivery and enabling experiments in conditions more closely matching clinical practice.</p>","PeriodicalId":20185,"journal":{"name":"Physics in medicine and biology","volume":" ","pages":""},"PeriodicalIF":3.3000,"publicationDate":"2025-06-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Physics in medicine and biology","FirstCategoryId":"5","ListUrlMain":"https://doi.org/10.1088/1361-6560/adea08","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ENGINEERING, BIOMEDICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: Preclinical small animal proton beam irradiation systems are increasingly in demand. However, the absence of dedicated systems comparable in precision to those in clinical settings presents a considerable hurdle to investigations in this field. To address this need, the SIRMIO project has developed a novel compact beam transport system configured to degrade and focus clinical proton beams. The beamline, about 1 meter long, housed in an environment to minimize scatter, includes degraders, collimators, and a permanent magnet quadrupole triplet to focus protons degraded from clinical energies. It is tailored to transport focused proton beams within the energy range of 20 to 50 MeV, ideal for small animal preclinical studies. The flexibility of this beamline design allows achieving beam-spot sizes of 1 mm sigma at the isocenter for all focused energies, with the particle fluence and spot sizes being variable through dynamic adjustment of the
collimator and magnetic lattice. 3-D scanning of the target volume is possible due to lateral beam scanning integrated into this design, without the use of additional scanning dipole magnets.
Approach: The beamline was optimized using an accelerator beam optics code, followed by a Monte Carlo model to account for beam-matter interactions. Using an experimentally validated clinical proton beam phase space as input, degraded beams are transported through the Monte Carlo model. Outcomes are assessed for beam characteristics and dosimetric properties Main Results: Beams transported by our proposed beamline design are shown to result in dosimetric properties suitable for preclinical studies, while also emulating realistic clinically relevant beam delivery scenarios like pencil beam scanning. Compared to a similar-sized collimator-only beamline, this design
enhances transmission and reduces secondary dose at the target due to absence of scattering elements nearby.
Significance: The portable SIRMIO beamline offers a flexible, precise alternative to passive methods for adapting clinical proton beams for small animal irradiation, enhancing preclinical research with clinically relevant beam delivery and enabling experiments in conditions more closely matching clinical practice.
目的:临床前小动物质子束辐照系统的需求日益增长。然而,缺乏可与临床环境中的精确系统相媲美的专用系统,这对该领域的研究构成了相当大的障碍。为了满足这一需求,SIRMIO项目开发了一种新型的紧凑型光束传输系统,用于降解和聚焦临床质子束。光束线大约1米长,安置在一个最小散射的环境中,包括降解器、准直器和一个永磁四极三重体,用于聚焦从临床能量中降解的质子。它专为传输能量范围在20至50兆电子伏的聚焦质子束而设计,是小动物临床前研究的理想选择。这种光束线设计的灵活性允许在所有聚焦能量的等心处实现1 mm sigma的光束光斑尺寸,通过动态调整
准直器和磁晶格,粒子的影响和光斑尺寸是可变的。由于侧束扫描集成到该设计中,无需使用额外的扫描偶极磁铁,因此可以对目标体积进行三维扫描。方法:使用加速器光束光学代码对光束线进行优化,然后使用蒙特卡罗模型来解释光束与物质的相互作用。利用实验验证的临床质子束相空间作为输入,退化的质子束通过蒙特卡罗模型传输。主要结果:通过我们提出的光束线设计传输的光束显示出适合临床前研究的剂量学特性,同时也模拟了现实的临床相关光束传输场景,如铅笔光束扫描。与类似尺寸的仅准直器光束线相比,该设计提高了透射率,并减少了目标处的二次剂量,因为附近没有散射元件。意义:便携式SIRMIO光束线提供了一种灵活、精确的替代被动方法,用于适应临床质子束用于小动物照射,加强临床相关光束输送的临床前研究,并使实验条件更接近临床实践。
期刊介绍:
The development and application of theoretical, computational and experimental physics to medicine, physiology and biology. Topics covered are: therapy physics (including ionizing and non-ionizing radiation); biomedical imaging (e.g. x-ray, magnetic resonance, ultrasound, optical and nuclear imaging); image-guided interventions; image reconstruction and analysis (including kinetic modelling); artificial intelligence in biomedical physics and analysis; nanoparticles in imaging and therapy; radiobiology; radiation protection and patient dose monitoring; radiation dosimetry