Bostel Tilman, Nicolay Nils H, Grossmann Jörg G, Mohr Angela, Delorme Stefan, Echner Gernot, Häring Peter, Debus Jürgen, Sterzing Florian
Clinical Cooperation Unit Radiation Oncology, German Cancer Research Center (DKFZ), Im Neuenheimer Feld 280, 69120 Heidelberg, Germany.
Radiat Oncol. 2014 Jan 9;9:12. doi: 10.1186/1748-717X-9-12.
The purpose of this clinical study is to investigate the clinical feasibility and safety of a shuttle-based MR-linac connection to provide MR-guided radiotherapy.
METHODS/DESIGN: A total of 40 patients with an indication for a neoadjuvant, adjuvant or definitive radiation treatment will be recruited including tumors of the head and neck region, thorax, upper gastrointestinal tract and pelvic region. All study patients will receive standard therapy, i.e. highly conformal radiation techniques like CT-guided intensity-modulated radiotherapy (IMRT) with or without concomitant chemotherapy or other antitumor medication, and additionally daily short MR scans in treatment position with the same immobilisation equipment used for irradiation for position verification and imaging of the anatomical and functional changes during the course of radiotherapy. For daily position control, skin marks and a stereotactic frame will be used for both imaging modalities. Patient transfer between the MR device and the linear accelerator will be performed with a shuttle system which uses an air-bearing patient platform for both procedures. The daily acquired MR and CT data sets will be digitally registrated, correlated with the planning CT and compared with each other regarding translational and rotational errors. Aim of this clinical study is to establish a shuttle-based approach for realising MR-guided radiotherapy for certain clinical situations. Second objectives are to compare MR-guided radiotherapy with the gold standard of CT image guidance for quality assurance of radiotherapy, to establish an appropriate MR protocol therefore, and to assess the possibility of using MR-based image guidance not only for position verification but also for adaptive strategies in radiotherapy.
Compared to CT, MRI might offer the advantage of providing IGRT without delivering an additional radiation dose to the patients and the possibility of optimisation of adaptive therapy strategies due to its superior soft tissue contrast. However, up to now, hybrid MR-linac devices are still under construction and not clinically applicable. For the near future, a shuttle-based approach would be a promising alternative for providing MR-guided radiotherapy, so that the present study was initiated to determine feasibility and safety of such an approach. Besides positioning information, daily MR data under treatment offer the possibility to assess tumor regression and functional parameters, with a potential impact not only on adaptive therapy strategies but also on early assessment of treatment response.
本临床研究的目的是探讨基于穿梭系统的磁共振直线加速器连接以提供磁共振引导放疗的临床可行性和安全性。
方法/设计:总共将招募40例有新辅助、辅助或根治性放射治疗指征的患者,包括头颈部、胸部、上消化道和盆腔区域的肿瘤。所有研究患者将接受标准治疗,即采用如CT引导的调强放疗(IMRT)等高度适形放疗技术,联合或不联合化疗或其他抗肿瘤药物,此外,在治疗体位进行每日短时间磁共振扫描,使用与放射治疗相同的固定设备进行体位验证,并在放疗过程中对解剖和功能变化进行成像。对于每日体位控制,两种成像方式均将使用皮肤标记和立体定向框架。磁共振设备和直线加速器之间的患者转运将通过穿梭系统进行,该系统在两种操作中均使用气浮患者平台。每日获取的磁共振和CT数据集将进行数字配准,与计划CT相关联,并就平移和旋转误差相互比较。本临床研究的目的是建立一种基于穿梭系统实现特定临床情况下磁共振引导放疗的方法。第二个目标是将磁共振引导放疗与CT图像引导的金标准进行比较,以确保放疗质量,因此建立合适的磁共振方案,并评估基于磁共振的图像引导不仅用于体位验证,还用于放疗中自适应策略的可能性。
与CT相比,MRI可能具有无需向患者额外提供辐射剂量即可提供图像引导放疗的优势,并且由于其卓越的软组织对比度,有可能优化自适应治疗策略。然而,到目前为止,混合磁共振直线加速器设备仍在建设中,尚未临床应用。在不久的将来,基于穿梭系统的方法将是提供磁共振引导放疗的一种有前景的替代方案,因此启动了本研究以确定这种方法的可行性和安全性。除了定位信息外,治疗期间的每日磁共振数据还提供了评估肿瘤退缩和功能参数的可能性,这不仅可能影响自适应治疗策略,还可能影响治疗反应的早期评估。