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First clinical implementation of real‐time, real anatomy tracking and radiation beam control

机译:实时,实际解剖跟踪和辐射束控制的第一次临床实施

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Purpose We describe the acceptance testing, commissioning, periodic quality assurance, and workflow procedures developed for the first clinically implemented magnetic resonance imaging‐guided radiation therapy ( MR ‐ IGRT ) system for real‐time tracking and beam control. Methods The system utilizes real‐time cine imaging capabilities at 4 frames per second for real‐time tracking and beam control. Testing of the system was performed using an in‐house developed motion platform and a commercially available motion phantom. Anatomical tracking is performed by first identifying a target (a region of interest that is either tissue to be treated or a critical structure) and generating a contour around it. A boundary contour is also created to identify tracking margins. The tracking algorithm deforms the anatomical contour (target or a normal organ) on every subsequent cine frame and compares it to the static boundary contour. If the anatomy of interest moves outside the boundary, the radiation delivery is halted until the tracked anatomy returns to treatment portal. The following were performed to validate and clinically implement the system: (a) spatial integrity evaluation; (b) tracking accuracy; (c) latency; (d) relative point dose and spatial dosimetry; (e) development of clinical workflow for gating; and (f) independent verification by an outside credentialing service. Results The spatial integrity of the MR system was found to be within 2?mm over a 45‐cm diameter field‐of‐view. The tracking accuracy for geometric targets was within 1.2?mm. The average system latency was measured to be within 394?ms. The dosimetric accuracy using ionization chambers was within 1.3%?±?1.7%, and the dosimetric spatial accuracy was within 2?mm. The phantom irradiation for the outside credentialing service had satisfactory results, as well. Conclusions The first clinical MR ‐ IGRT system was validated for real‐time tracking and gating capabilities and shown to be reliable and accurate. Patient workflow methods were developed for efficient treatment. Periodic quality assurance tests can be efficiently performed with commercially available equipment to ensure accurate system performance.
机译:目的,我们描述了为第一个临床实施的磁共振成像引导辐射治疗(MR-IGRT)系统开发的验收测试,调试,定期质量保证和工作流程,用于实时跟踪和光束控制。方法该系统在每秒4帧中使用实时连续成像能力,用于实时跟踪和光束控制。使用内部开发的运动平台和市售的运动模型进行系统测试。通过首先识别目标(是待处理的组织或临界结构的感兴趣区域或临界结构的感兴趣区域)来执行解剖学跟踪,并在其周围产生轮廓。还创建了边界轮廓以识别跟踪边距。跟踪算法将解剖轮廓(目标或正常器官)在每个后续的调整帧上变形并将其与静态边界轮廓进行比较。如果利息的解剖学在边界外移动,则会停止辐射递送,直到跟踪的解剖学返回治疗门户。执行以下内容以验证和临床实施系统:(a)空间完整性评估; (b)跟踪准确性; (c)延迟; (d)相对点剂量和空间剂量计; (e)改编临床工作流程的开发; (f)通过外部资本服务独立核实。结果MR系统的空间完整性被发现在45厘米直径的视野下,在25厘米的范围内。几何目标的跟踪精度在1.2?mm内。测量平均系统延迟在394内?MS。使用电离室的剂量测量精度在1.3%Δ±1.7%之内,并且剂量空间精度在2?mm内。外部资深服务的幻影辐照也有令人满意的结果。结论验证了第一临床MR-IGRT系统,用于实时跟踪和门控功能,并显示可靠和准确。开发了患者工作流程方法以有效处理。定期质量保证测试可以通过商用设备有效地进行,以确保精确的系统性能。

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