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Safety and efficacy of fiducial marker implantation for robotic stereotactic body radiation therapy with fiducial tracking

机译:基准跟踪技术在机器人立体定向身体放射治疗中的基准标记植入安全性和有效性

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The purpose of this study was to assess the feasibility, efficacy and toxicity of fiducial marker implantation and tracking in CyberKnife? stereotactic radiation therapy (SBRT) applied to extracranial locations. This is a retrospective, single-centre, observational study to collect the data of all patients treated by stereotactic radiation therapy with fiducial marker tracking at extracranial locations, conducted between June 2014 and November 2017. Information regarding the implantation procedure, the types of toxicity related to marker implantation and the number of markers implanted/tracked during treatment were collected. Complication rates were evaluated using the CTCAE v4 [Common Terminology Criteria for Adverse Events] scale. The technical success rate was based on the ability to optimally track the tumor throughout all treatment fractions. Out of 2505 patients treated by stereotactic radiation therapy, 25% received treatment with fiducial marker tracking. The total number of implantation procedures was 616 and 1543 fiducial markers were implanted. The implantation-related complication rate was 3%, with 16 Grade 1 events and 4 Grade 2 events. The number of treated patients and the number of implanted markers has gradually increased since the technique was first implemented. The median treatment time was 27?min (range 10–76). 1295 fiducials were effectively tracked throughout all treatment fractions, corresponding to a technical success rate of 84%. The difference between the number of fiducials implanted and those tracked during treatment decreased significantly as the site’s experience increased. Fiducial marker implantation and tracking is feasible, well-tolerated, and technically effective technique in SBRT for extracranial tumors.
机译:这项研究的目的是评估在射波刀中基准标记植入和追踪的可行性,功效和毒性。立体定向放射疗法(SBRT)应用于颅外部位。这是一项回顾性,单中心,观察性研究,旨在收集2014年6月至2017年11月之间在颅外位置进行立体定向放射治疗并进行基准标记跟踪的所有患者的数据。有关植入程序,毒性相关类型的信息收集标记物,并收集治疗期间植入/追踪的标记物数目。使用CTCAE v4 [不良事件通用术语标准]量表评估并发症发生率。技术成功率是基于在所有治疗方案中最佳跟踪肿瘤的能力。在2505例接受立体定向放射治疗的患者中,有25%接受了基准标记跟踪治疗。植入程序的总数为616,并且植入了1543个基准标记。与植入有关的并发症发生率为3%,其中16例1级事件和4例2级事件。自从首次实施该技术以来,治疗的患者数量和植入的标记物数量已逐渐增加。中位治疗时间为27分钟(范围10-76)。在所有治疗环节中,有效跟踪了1295个基准点,对应的技术成功率为84%。随着现场经验的增加,植入的基准点数与治疗期间追踪的基准点数之间的差异显着减少。基准标记物植入和跟踪在颅外肿瘤中是可行的,耐受性良好且技术上有效的技术。

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