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

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...

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Autores principales: Rief, Harald, Katayama, Sonja, Bruckner, Thomas, Rieken, Stefan, Bostel, Tilman, Förster, Robert, Schlampp, Ingmar, Wolf, Robert, Debus, Jürgen, Sterzing, Florian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465731/
https://www.ncbi.nlm.nih.gov/pubmed/26054533
http://dx.doi.org/10.1186/s13063-015-0761-7
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author Rief, Harald
Katayama, Sonja
Bruckner, Thomas
Rieken, Stefan
Bostel, Tilman
Förster, Robert
Schlampp, Ingmar
Wolf, Robert
Debus, Jürgen
Sterzing, Florian
author_facet Rief, Harald
Katayama, Sonja
Bruckner, Thomas
Rieken, Stefan
Bostel, Tilman
Förster, Robert
Schlampp, Ingmar
Wolf, Robert
Debus, Jürgen
Sterzing, Florian
author_sort Rief, Harald
collection PubMed
description 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).
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spelling pubmed-44657312015-06-15 High-dose single-fraction IMRT versus fractionated external beam radiotherapy for patients with spinal bone metastases: study protocol for a randomized controlled trial Rief, Harald Katayama, Sonja Bruckner, Thomas Rieken, Stefan Bostel, Tilman Förster, Robert Schlampp, Ingmar Wolf, Robert Debus, Jürgen Sterzing, Florian Trials Study Protocol 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). BioMed Central 2015-06-09 /pmc/articles/PMC4465731/ /pubmed/26054533 http://dx.doi.org/10.1186/s13063-015-0761-7 Text en © Rief et al. 2015 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Study Protocol
Rief, Harald
Katayama, Sonja
Bruckner, Thomas
Rieken, Stefan
Bostel, Tilman
Förster, Robert
Schlampp, Ingmar
Wolf, Robert
Debus, Jürgen
Sterzing, Florian
High-dose single-fraction IMRT versus fractionated external beam radiotherapy for patients with spinal bone metastases: study protocol for a randomized controlled trial
title High-dose single-fraction IMRT versus fractionated external beam radiotherapy for patients with spinal bone metastases: study protocol for a randomized controlled trial
title_full High-dose single-fraction IMRT versus fractionated external beam radiotherapy for patients with spinal bone metastases: study protocol for a randomized controlled trial
title_fullStr High-dose single-fraction IMRT versus fractionated external beam radiotherapy for patients with spinal bone metastases: study protocol for a randomized controlled trial
title_full_unstemmed High-dose single-fraction IMRT versus fractionated external beam radiotherapy for patients with spinal bone metastases: study protocol for a randomized controlled trial
title_short High-dose single-fraction IMRT versus fractionated external beam radiotherapy for patients with spinal bone metastases: study protocol for a randomized controlled trial
title_sort high-dose single-fraction imrt versus fractionated external beam radiotherapy for patients with spinal bone metastases: study protocol for a randomized controlled trial
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4465731/
https://www.ncbi.nlm.nih.gov/pubmed/26054533
http://dx.doi.org/10.1186/s13063-015-0761-7
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