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Radiation-induced toxicity after image-guided and intensity-modulated radiotherapy versus external beam radiotherapy for patients with spinal bone metastases (IRON-1): a study protocol for a randomized controlled pilot trial

机译:影像引导和强度调制放疗与外照射对脊柱骨转移患者(IRON-1)的放射诱导毒性:一项随机对照试验研究的研究方案

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摘要

Background: Radiation therapy (RT) of bone metastases provides an important treatment approach in palliative care treatment concepts. As a consequence of treatment, the extent of radiation-induced toxicity is a crucial feature with consequences to a patient’s quality of life. In this context this study aims at reducing the extent of radiation-induced side effects and toxicity by assuming a better sparing of normal tissue with the use of intensity-modulated instead of conventionally delivered external beam radiotherapy. Methods/design: In this prospective, randomized, single-center trial for patients with spinal bone metastases, RT is performed as either image-guided intensity-modulated radiotherapy (10x3Gy) or conventionally fractionated external beam radiotherapy (10x3Gy). Afterwards radiation-induced toxicity will be assessed and compared 3 and 6 months after the end of radiation. Discussion: The aim of this pilot study is the evaluation of achievable benefits, with reduced radiation toxicity being the primary endpoint in the comparison of intensity-modulated radiotherapy versus conventional radiotherapy for patients with spinal bone metastases. Secondarily, bone re-calcification, quality of life, pain relief, spinal instability, and local control will be measured and compared between the two treatment groups. Trial registration: ClinicalTrials.gov, NCT02832830. Registered on 12 July 2016.
机译:背景:骨转移的放射治疗(RT)提供了姑息治疗概念中的重要治疗方法。作为治疗的结果,辐射诱发的毒性程度是至关重要的特征,对患者的生活质量有影响。在这种情况下,本研究旨在通过假设强度组织更好地保留正常组织,而不是采用传统的外照射治疗,以减少辐射引起的副作用和毒性。方法/设计:在这项针对脊椎骨转移患者的前瞻性,随机,单中心试验中,RT是以图像指导的强度调制放疗(10x3Gy)或常规分级外照射(10x3Gy)进行。此后,将评估放疗结束后3个月和6个月的放疗毒性,并进行比较。讨论:这项初步研究的目的是评估可获得的益处,在对比强度调制放射疗法与传统放射疗法治疗脊柱骨转移患者时,降低放射毒性是主要终点。其次,将测量并比较两个治疗组之间的骨再钙化,生活质量,疼痛缓解,脊柱不稳和局部控制。试用注册:ClinicalTrials.gov,NCT02832830。 2016年7月12日注册。

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