Orlando Nathan, Crosby Jennie, Glide-Hurst Carri, Culberson Wesley, Sarfehnia Arman
Odette Cancer Centre, Sunnybrook Health Sciences Centre, Toronto, Ontario, Canada.
Department of Radiation Oncology, University of Toronto, Toronto, Ontario, Canada.
J Appl Clin Med Phys. 2025 Mar;26(3):e14613. doi: 10.1002/acm2.14613. Epub 2024 Dec 14.
The purpose of this work was to experimentally quantify MR-compatible ionization chamber response for 1.5T Elekta Unity and 0.35T ViewRay MRIdian MR-linac systems through the determination of the magnetic field quality conversion factor, k.
Seven MR-compatible ionization chamber models from Standard Imaging and PTW were evaluated. Both the quality conversion factor k and the magnetic field quality conversion factor k were experimentally determined through a cross-calibration method. Specifically, the ratio of absorbed dose measured with a reference A1SL chamber under reference conditions to corrected output measured with each test chamber at the same point of measurement allowed for the determination of k. The angular dependence of the magnetic field quality conversion factor for MR-compatible chamber models was assessed for the 1.5T Elekta Unity system by measuring k with the chamber axis and magnetic field direction aligned at cardinal angles (0°, 90°, 180°, 270°).
Beam quality conversion (k) factors for MR-compatible ionization chambers measured in a standard linac beam showed an average percent difference of -0.09 ± 0.18% compared to computed k values for their conventional chamber versions. Similarly, magnetic field quality conversion (k) factors for corresponding MR and non-MR ionization chamber models measured using the same cross-calibration technique demonstrated average percent differences of -0.1 ± 0.3% and 0.0 ± 0.2% for the Elekta Unity and ViewRay MRIdian, respectively. Investigation of the angular dependence of this correction factor demonstrated identical chamber response for equivalent MR-compatible and conventional chamber models.
This work provides critical experimental validation of MR-compatible ionization chamber performance, with a direct comparison of measured k values to corresponding conventional chamber models demonstrating nearly equivalent chamber response. k values determined using our experimental method will serve as an important reference for upcoming MR-linac reference dosimetry protocols and ultimately represent an important step towards accurate output calibration of MR-linac systems.
本研究旨在通过测定磁场质量转换因子k,对1.5T的医科达Unity和0.35T的ViewRay MRIdian MR直线加速器系统的磁共振兼容电离室响应进行实验量化。
对来自标准成像公司和PTW公司的7种磁共振兼容电离室模型进行了评估。通过交叉校准方法实验测定了质量转换因子k和磁场质量转换因子k。具体而言,用参考A1SL电离室在参考条件下测量的吸收剂量与在同一点用每个测试电离室测量的校正输出之比,可用于确定k。对于1.5T的医科达Unity系统,通过将电离室轴与磁场方向对齐在基本角度(0°、90°、180°、270°)测量k,评估了磁共振兼容电离室模型的磁场质量转换因子的角度依赖性。
在标准直线加速器射束中测量的磁共振兼容电离室的射束质量转换(k)因子,与其传统电离室版本的计算k值相比,平均百分比差异为-0.09±0.18%。同样,使用相同交叉校准技术测量的相应磁共振和非磁共振电离室模型的磁场质量转换(k)因子,医科达Unity和ViewRay MRIdian的平均百分比差异分别为-0.1±0.3%和0.0±0.2%。对该校正因子角度依赖性的研究表明,等效的磁共振兼容电离室和传统电离室模型具有相同的电离室响应。
本研究为磁共振兼容电离室性能提供了关键的实验验证,将测量的k值与相应的传统电离室模型直接比较,结果表明电离室响应几乎等效。使用我们的实验方法确定的k值将作为即将出台的MR直线加速器参考剂量学方案的重要参考,最终代表了迈向MR直线加速器系统准确输出校准的重要一步。