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高剂量单次分割调强放射治疗与分次外照射放疗用于脊柱骨转移患者的比较:一项随机对照试验的研究方案

High-dose single-fraction IMRT versus fractionated external beam radiotherapy for patients with spinal bone metastases: study protocol for a randomized controlled trial.

作者信息

Rief Harald, Katayama Sonja, Bruckner Thomas, Rieken Stefan, Bostel Tilman, Förster Robert, Schlampp Ingmar, Wolf Robert, Debus Jürgen, Sterzing Florian

机构信息

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

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

出版信息

Trials. 2015 Jun 9;16:264. doi: 10.1186/s13063-015-0761-7.

Abstract

BACKGROUND

Stereotactic body radiation therapy (SBRT)using intensity-modulated radiotherapy (IMRT) can be a safe modality for treating spinal bone metastasis with enhanced targeting accuracy and an effective method for achieving good tumor control and a rigorous pain response.

METHODS/DESIGN: This is a single-center, prospective randomized controlled trial to evaluate pain relief after RT and consists of two treatment groups with 30 patients in each group. One group will receive single-fraction intensity-modulated RT with 1 × 24 Gy, and the other will receive fractionated RT with 10 × 3 Gy. The target parameters will be measured at baseline and at 3 and 6 months after RT.

DISCUSSION

The aim of this study is to evaluate pain relief after RT in patients with spinal bone metastases by means of two different techniques: stereotactic body radiation therapy and fractionated RT. The primary endpoint is pain relief at the 3-month time-point after RT. Secondly, quality of life, fatigue, overall and bone survival, and local control will be assessed.

TRIAL REGISTRATION

ClinicalTrials.gov identifier NCT02358720 (June 2, 2015).

摘要

背景

采用调强放疗(IMRT)的立体定向体部放疗(SBRT)对于治疗脊柱骨转移瘤而言可能是一种安全的方式,其靶向准确性更高,也是实现良好肿瘤控制和严格疼痛缓解的有效方法。

方法/设计:这是一项单中心前瞻性随机对照试验,旨在评估放疗后的疼痛缓解情况,包括两个治疗组,每组30例患者。一组将接受单次分割调强放疗,剂量为1×24 Gy,另一组将接受分次放疗,剂量为10×3 Gy。将在基线以及放疗后3个月和6个月测量目标参数。

讨论

本研究的目的是通过两种不同技术(立体定向体部放疗和分次放疗)评估脊柱骨转移瘤患者放疗后的疼痛缓解情况。主要终点是放疗后3个月时间点的疼痛缓解情况。其次,将评估生活质量、疲劳、总体生存和骨生存以及局部控制情况。

试验注册

ClinicalTrials.gov标识符NCT02358720(2015年6月2日)。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/380f/4465731/e685b43cfe04/13063_2015_761_Fig1_HTML.jpg

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