SMILE-stereotactic multiple fraction radiotherapy for non-spine bone metastases: study protocol for a multicenter, open-label phase III randomized controlled trial.

IF 2 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL
Trials Pub Date : 2024-11-13 DOI:10.1186/s13063-024-08608-6
Robert Foerster, Daniel R Zwahlen, Christina Schroeder, Paul Windisch, Marc-Eric Halatsch, Alex Alfieri, Christoph Meier, Hossein Hemmatazad, Daniel M Aebersold, André Buchali, Daniel Habermehl, Nidar Batifi
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引用次数: 0

Abstract

Background: The SMILE study addresses a significant need in palliative oncology by evaluating the non-inferiority of a shortened, 3-fraction stereotactic body radiotherapy (SBRT) schedule against the traditional 5-fraction approach for non-spine bone metastases in terms of pain control. Optimizing SBRT could significantly enhance the quality of life for patients by providing effective pain relief while minimizing treatment sessions.

Methods: This international, multicenter phase III trial will randomize 162 patients to receive either a 3-fraction regimen (9 Gy per fraction) or a standard 5-fraction regimen (7 Gy per fraction). Outcomes, assessed at 3 months post-treatment, will focus on pain response, quality of life, and control of metastasis. With a hypothesis-driven design, the study will incorporate intent-to-treat and per-protocol analyses, incorporating appropriate measures for data integrity and handling of missing information.

Discussion: If the 3-fraction SBRT regimen demonstrates non-inferiority, it could streamline palliative care protocols, reduce patient burden, and set a new standard for treatment, reflecting a patient-centered approach in palliative radiation oncology.

Trial registration: The trial has been registered prospectively on ClinicalTrials.gov under the identifier NCT05406063, as of May 3, 2022.

SMILE-立体定向多分割放射治疗非脊柱骨转移瘤:多中心、开放标签 III 期随机对照试验的研究方案。
研究背景SMILE研究通过评估缩短的3分次立体定向体放射治疗(SBRT)计划与治疗非脊柱骨转移瘤的传统5分次方法在疼痛控制方面的非劣势,满足了姑息肿瘤学的重大需求。优化 SBRT 可以有效缓解疼痛,同时减少治疗次数,从而显著提高患者的生活质量:这项国际多中心 III 期试验将随机抽取 162 名患者,让他们接受 3 次分次治疗方案(每次 9 Gy)或标准 5 次分次治疗方案(每次 7 Gy)。结果将在治疗后 3 个月进行评估,重点关注疼痛反应、生活质量和转移控制。该研究采用假设驱动设计,将进行意向治疗分析和按方案分析,并采取适当措施确保数据完整性和处理缺失信息:讨论:如果3分次SBRT方案显示出非劣效性,则可简化姑息治疗方案,减轻患者负担,并制定新的治疗标准,体现姑息放射肿瘤学中以患者为中心的方法:截至2022年5月3日,该试验已在ClinicalTrials.gov上进行了前瞻性注册,标识符为NCT05406063。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Trials
Trials 医学-医学:研究与实验
CiteScore
3.80
自引率
4.00%
发文量
966
审稿时长
6 months
期刊介绍: Trials is an open access, peer-reviewed, online journal that will encompass all aspects of the performance and findings of randomized controlled trials. Trials will experiment with, and then refine, innovative approaches to improving communication about trials. We are keen to move beyond publishing traditional trial results articles (although these will be included). We believe this represents an exciting opportunity to advance the science and reporting of trials. Prior to 2006, Trials was published as Current Controlled Trials in Cardiovascular Medicine (CCTCVM). All published CCTCVM articles are available via the Trials website and citations to CCTCVM article URLs will continue to be supported.
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