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脊柱骨转移患者调强放疗联合局部加量:一项随机对照试验的研究方案。

Intensity-modulated radiotherapy with integrated-boost in patients with bone metastasis of the spine: study protocol for a randomized controlled trial.

机构信息

Department of Radiation Oncology, University Hospital Heidelberg, Im Neuenheimer Feld 400, 69120, Heidelberg, Germany.

Department of Medical Biometry, University Hospital Heidelberg, Im Neuenheimer Feld 305, 69120, Heidelberg, Germany.

出版信息

Trials. 2018 Jan 22;19(1):59. doi: 10.1186/s13063-018-2452-7.

Abstract

BACKGROUND

Stereotactic body radiation therapy (SBRT) using intensity-modulated radiotherapy (IMRT) with dose escalation by simultaneous integrated boost (SIB) can be a safe modality for treating spinal bone metastases with enhanced targeting accuracy and improve local tumor control.

METHODS/DESIGN: This is a single-center, prospective, randomized, controlled trial. One hundred and twenty patients with spinal bone metastases will receive palliative radiation therapy at the Heidelberg University Hospital. SBRT will be given in five or ten fractions with or without SIB. Four treatment arms are planned: IMRT with 30 Gy in ten fractions, IMRT with 30 Gy in ten fractions and SIB to 40 Gy, IMRT with 20 Gy in five fractions, and IMRT with 20 Gy in five fractions and SIB to 30Gy in five fractions will be compared. The target parameters will be measured at baseline level and at three and six months after radiation.

DISCUSSION

The primary endpoint of this study was to assess and compare the local tumor control (by means of different fractionation schedules and biological doses to the tumor area). Secondary endpoints are acute and chronic adverse events, pain relief, quality of life, and fatigue.

TRIAL REGISTRATION

ClinicalTrials.gov, NCT02832765 . Registered on 27 July 2016.

摘要

背景

使用调强放疗(IMRT)进行立体定向体放射治疗(SBRT),通过同步整合boost(SIB)进行剂量递增,对于治疗脊柱骨转移瘤具有增强的靶向准确性和提高局部肿瘤控制的安全性。

方法/设计:这是一项单中心、前瞻性、随机、对照试验。120 名脊柱骨转移患者将在海德堡大学医院接受姑息性放射治疗。SBRT 将采用 5 或 10 个分次进行,或采用 SIB。计划了 4 个治疗组:IMRT 单次 30Gy,IMRT 单次 30Gy 并 SIB 至 40Gy,IMRT 单次 20Gy,和 IMRT 单次 20Gy 并 SIB 至 30Gy。将比较这 4 种治疗方案。将在基线水平以及放射治疗后 3 个月和 6 个月测量靶区参数。

讨论

该研究的主要终点是评估和比较局部肿瘤控制(通过不同的分割方案和肿瘤区域的生物剂量)。次要终点是急性和慢性不良反应、疼痛缓解、生活质量和疲劳。

试验注册

ClinicalTrials.gov,NCT02832765。于 2016 年 7 月 27 日注册。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/319d/5778628/99abce6ade3a/13063_2018_2452_Fig1_HTML.jpg

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