现代放射治疗技术时代的骨转移半身照射 (HBI) - 系统综述

IF 2.7 3区 医学 Q3 ONCOLOGY
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引用次数: 0

摘要

骨转移(BMs)是导致癌症相关疼痛的最常见原因,而放射治疗在治疗骨转移引起的疼痛方面发挥着关键作用。半身照射(HBI)是一种可用于治疗多发性骨转移疼痛患者的方式。在现代,对毒性的担忧和需要骨髓功能健全的新药的出现限制了半身照射在晚期癌症中的应用。对 HBI 毒性的担忧源于过时的技术;现在,体积调制弧治疗(VMAT)和螺旋断层治疗等现代方法可以更安全地照射复杂的靶体积。我们进行了一项系统性回顾,以介绍有关 HBI 疗效和潜在毒性的最新信息。疼痛通常在 HBI 治疗后 2-3 周内迅速缓解。所有系列的总体疼痛反应率都很高,中位数为 84%(75.6-89%),完全疼痛反应率中位数为 36%。毒性通常仅限于 G1/G2,G3 病例非常罕见。50%以上的患者在接受 HBI 治疗后可以减少镇痛剂的摄入量。此外,借助现代放疗技术,大多数患者的生活质量都得到了改善。HBI 是一种安全有效的方法,应再次考虑更频繁地使用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Half body irradiation (HBI) for bone metastases in the modern radiotherapy technique era – A systematic review

Bone metastases (BMs) are the most common cause of cancer-related pain and radiation therapy plays a key role in treating pain caused by it. The half-body irradiation (HBI) is a modality that can be used to treat patients with multiple painful BMs. In the modern era, concerns about toxicity and the availability of new agents requiring robust bone marrow function have limited the use of HBI in advanced cancer. Concerns about HBI toxicity stem from outdated techniques; modern methods like volumetric modulated arc therapy (VMAT) and helical tomotherapy now allow safer irradiation of complex target volumes. We conducted a systematic review to present updated information about HBI efficacy and potential toxicity. Pain relief usually occurs very quickly 2–3 weeks after HBI. The overall pain response rate was high in all the series, accounting for a median of 84 % (75.6–89 %), with a median of 36 % complete pain response. The toxicity is usually limited to G1/G2, with very rare G3 cases. More than 50 % of patients can reduce analgesic intake after HBI. Additionally, with modern radiotherapy techniques, quality of life is improved in most patients. HBI is a safe and effective method and should once again be reconsidered for more frequent use.

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来源期刊
Clinical and Translational Radiation Oncology
Clinical and Translational Radiation Oncology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
5.30
自引率
3.20%
发文量
114
审稿时长
40 days
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