Danish Centre for Particle Therapy, Aarhus University Hospital, Aarhus, Denmark.
Department of Clinical Medicine, Faculty of Health, Aarhus University, Aarhus, Denmark.
Med Phys. 2024 Jul;51(7):5119-5129. doi: 10.1002/mp.17049. Epub 2024 Apr 3.
Dosimetry in pre-clinical FLASH studies is essential for understanding the beam delivery conditions that trigger the FLASH effect. Resolving the spatial and temporal characteristics of proton pencil beam scanning (PBS) irradiations with ultra-high dose rates (UHDR) requires a detector with high spatial and temporal resolution.
To implement a novel camera-based system for time-resolved two-dimensional (2D) monitoring and apply it in vivo during pre-clinical proton PBS mouse irradiations.
Time-resolved 2D beam monitoring was performed with a scintillation imaging system consisting of a 1 mm thick transparent scintillating sheet, imaged by a CMOS camera. The sheet was placed in a water bath perpendicular to a horizontal PBS proton beam axis. The scintillation light was reflected through a system of mirrors and captured by the camera with 500 frames per second (fps) for UHDR and 4 fps for conventional dose rates. The raw images were background subtracted, geometrically transformed, flat field corrected, and spatially filtered. The system was used for 2D spot and field profile measurements and compared to radiochromic films. Furthermore, spot positions were measured for UHDR irradiations. The measured spot positions were compared to the planned positions and the relative instantaneous dose rate to equivalent fiber-coupled point scintillator measurements. For in vivo application, the scintillating sheet was placed 1 cm upstream the right hind leg of non-anaesthetized mice submerged in the water bath. The mouse leg and sheet were both placed in a 5 cm wide spread-out Bragg peak formed from the mono-energetic proton beam by a 2D range modulator. The mouse leg position within the field was identified for both conventional and FLASH irradiations. For the conventional irradiations, the mouse foot position was tracked throughout the beam delivery, which took place through repainting. For FLASH irradiations, the delivered spot positions and relative instantaneous dose rate were measured.
The pixel size was 0.1 mm for all measurements. The spot and field profiles measured with the scintillating sheet agreed with radiochromic films within 0.4 mm. The standard deviation between measured and planned spot positions was 0.26 mm and 0.35 mm in the horizontal and vertical direction, respectively. The measured relative instantaneous dose rate showed a linear relation with the fiber-coupled scintillator measurements. For in vivo use, the leg position within the field varied between mice, and leg movement up to 3 mm was detected during the prolonged conventional irradiations.
The scintillation imaging system allowed for monitoring of UHDR proton PBS delivery in vivo with 0.1 mm pixel size and 2 ms temporal resolution. The feasibility of instantaneous dose rate measurements was demonstrated, and the system was used for validation of the mouse leg position within the field.
在临床前 FLASH 研究中,剂量学对于理解引发 FLASH 效应的束流输送条件至关重要。为了解析超高剂量率(UHDR)质子铅笔束扫描(PBS)照射的时空特性,需要使用具有高时空分辨率的探测器。
实施一种新的基于相机的系统,用于实时二维(2D)监测,并在临床前质子 PBS 小鼠照射过程中进行体内应用。
采用由 1 毫米厚的透明闪烁片组成的闪烁成像系统进行时间分辨 2D 束流监测,并通过 CMOS 相机进行成像。该薄片放置在与水平 PBS 质子束轴垂直的水浴中。闪烁光通过一系列镜子反射,并由相机以 500 帧/秒(fps)的速度捕获,用于 UHDR,以 4 fps 的速度用于常规剂量率。对原始图像进行背景减除、几何变换、平场校正和空间滤波。该系统用于二维点和场轮廓测量,并与光致变色胶片进行比较。此外,还对点位置进行了 UHDR 照射测量。测量的点位置与计划位置以及与等效光纤耦合点闪烁体测量的相对瞬时剂量率进行比较。为了体内应用,将闪烁片放置在浸没在水浴中的非麻醉小鼠的右后腿上游 1 厘米处。将小鼠腿和薄片都放置在二维范围调制器形成的单能质子束的 5 厘米宽扩展布拉格峰中。在常规和 FLASH 照射下,确定了场内小鼠腿的位置。对于常规照射,在通过重新绘制进行束流输送的过程中,跟踪了鼠标脚的位置。对于 FLASH 照射,测量了所传递的点位置和相对瞬时剂量率。
所有测量的像素大小均为 0.1 毫米。用闪烁片测量的点和场轮廓与光致变色胶片的偏差在 0.4 毫米以内。测量和计划点位置之间的标准差分别为 0.26 毫米和 0.35 毫米,水平和垂直方向。测量的相对瞬时剂量率与光纤耦合闪烁体测量呈线性关系。对于体内应用,场中鼠标腿的位置在不同的小鼠之间有所变化,并且在长时间的常规照射过程中检测到腿的移动高达 3 毫米。
闪烁成像系统允许使用 0.1 毫米像素大小和 2 毫秒时间分辨率进行体内超高剂量率质子 PBS 输送的实时监测。证明了瞬时剂量率测量的可行性,并使用该系统验证了场中鼠标腿的位置。