首页> 外文期刊>Radiotherapy and oncology: Journal of the European Society for Therapeutic Radiology and Oncology >Credentialing of radiotherapy centres for a clinical trial of adaptive radiotherapy for bladder cancer (TROG 10.01)
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Credentialing of radiotherapy centres for a clinical trial of adaptive radiotherapy for bladder cancer (TROG 10.01)

机译:放射治疗中心对膀胱癌适应性放射治疗的临床试验的认证(TROG 10.01)

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Background: Daily variations in bladder filling make conformal treatment of bladder cancer challenging. On-line adaptive radiotherapy with a choice of plans has been demonstrated to reduce small bowel irradiation in single institution trials. In order to support a multicentre feasibility clinical trial on adaptive radiotherapy for bladder cancer (TROG 10.01) a credentialing programme was developed for centres wishing to participate. Methods: The credentialing programme entails three components: a facility questionnaire; a planning exercise which tests the ability of centres to create three adaptive plans based on a planning and five cone beam CTs; and a site visit during which image quality, imaging dose and image guidance procedures are assessed. Image quality and decision making were tested using customised inserts for a Perspex phantom (Modus QUASAR) that mimic different bladder sizes. Dose was assessed in the same phantom using thermoluminescence dosimetry (TLD). Results: All 12 centres participating in the full credentialing programme were able to generate appropriate target volumes in the planning exercise and identify the correct target volume and position the bladder phantom in the phantom within 3 mm accuracy. None of the imaging doses exceeded the limit of 5 cGy with a CT on rails system having the lowest overall dose. Conclusion: A phantom mimicking the decision making process for adaptive radiotherapy was found to be well suited during site visits for credentialing of centres participating in a clinical trial of adaptive radiotherapy for bladder cancer. Combined with a planning exercise the site visit allowed testing the ability of centres to create adaptive treatment plans and make appropriate decisions based on the volumetric images acquired at treatment.
机译:背景:膀胱填充物的每日变化使保形治疗膀胱癌具有挑战性。在单个机构的试验中,已经证明可以选择计划的在线自适应放射疗法可以减少小肠辐射。为了支持针对膀胱癌的适应性放射治疗的多中心可行性临床试验(TROG 10.01),针对希望参与的中心制定了认证计划。方法:认证程序包括三个部分:设施调查表;计划活动,测试中心基于计划和五个锥束CT创建三个适应计划的能力;进行现场访问,评估图像质量,成像剂量和图像指导程序。使用用于模拟不同膀胱尺寸的有机玻璃体模(Modus QUASAR)的定制插件测试了图像质量和决策能力。使用热致发光剂量法(TLD)在同一体模中评估剂量。结果:参加完整认证计划的所有12个中心都能够在计划工作中生成适当的目标体积,并确定正确的目标体积,并将膀胱体模放置在体模中,精度在3 mm以内。使用轨道上CT的总剂量最低的成像剂量均不会超过5 cGy的限制。结论:模拟适应性放射疗法的决策过程的幻影被发现非常适合在现场访问期间对参加适应性放射疗法的膀胱癌临床试验中心进行认证。结合计划演习,现场访问可以测试中心制定适应性治疗计划并根据治疗时获得的容积图像做出适当决策的能力。

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