Safety and efficacy of iridium-192 high-dose-rate interstitial brachytherapy for pleural and chest wall tumours: preliminary results.

IF 1.1 4区 医学 Q4 ONCOLOGY
Journal of Contemporary Brachytherapy Pub Date : 2025-08-01 Epub Date: 2025-08-26 DOI:10.5114/jcb.2025.153852
Jing Zhang, Bin Chen, Sheng Lin, Haowen Pang, Xiangxiang Shi
{"title":"Safety and efficacy of iridium-192 high-dose-rate interstitial brachytherapy for pleural and chest wall tumours: preliminary results.","authors":"Jing Zhang, Bin Chen, Sheng Lin, Haowen Pang, Xiangxiang Shi","doi":"10.5114/jcb.2025.153852","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>To evaluate the safety and efficacy of computed tomography (CT)-guided iridium-192 (<sup>192</sup>Ir) high-dose-rate (HDR) interstitial brachytherapy (ISBT) for pleural and chest wall malignant tumours.</p><p><strong>Material and methods: </strong>This single-centre retrospective cohort study involved 21 patients with pleural/chest wall malignant tumours treated between January 2024 and January 2025. All patients underwent HDR ISBT (30 Gy in a single fraction). Treatment included CT-guided needle implantation, three-dimensional dose optimisation (Oncentra system), and adherence to Radiation Therapy Oncology Group dose constraints for organs at risk (OARs). Efficacy endpoints included objective response (Response Evaluation Criteria in Solid Tumours v1.1), pain relief (Numerical Rating Scale), and dosimetric comparison with virtual stereotactic body radiotherapy. Safety was assessed using the Radiation Therapy Oncology Group/European Organisation for Research and Treatment of Cancer toxicity criteria.</p><p><strong>Results: </strong>The median follow-up duration was 7.48 months. The objective response rate (complete response + partial response) was 76.19%, with 28.57% achieving a complete response and 47.62% achieving a partial response. Pain relief was achieved in 87.5% of patients with pretreatment pain, with numerical rating scale scores decreasing from moderate to severe (median, 6) to mild (median, 3) at 1 month. No ≥ grade II complications (e.g. bronchopleural fistula, pneumothorax) occurred; only four patients experienced minor subcutaneous haemorrhage/emphysema. Dosimetric analysis showed a significantly higher target mean dose with ISBT than with stereotactic body radiotherapy (<i>p</i> < 0.001), while OARs doses (e.g. lungs, heart, spinal cord) remained within Radiation Therapy Oncology Group limits. Rib and chest wall dose exceedances were rare and clinically insignificant.</p><p><strong>Conclusions: </strong>Computed tomography-guided <sup>192</sup>Ir HDR ISBT offers safe, effective local control and rapid pain relief for pleural/chest wall tumours, demonstrating superior dosimetric conformity and lower toxicity to OARs. This minimally invasive approach is a viable option for patients unsuitable for surgery or external beam radiotherapy.</p>","PeriodicalId":51305,"journal":{"name":"Journal of Contemporary Brachytherapy","volume":"17 4","pages":"213-220"},"PeriodicalIF":1.1000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12489535/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Contemporary Brachytherapy","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.5114/jcb.2025.153852","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/26 0:00:00","PubModel":"Epub","JCR":"Q4","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Purpose: To evaluate the safety and efficacy of computed tomography (CT)-guided iridium-192 (192Ir) high-dose-rate (HDR) interstitial brachytherapy (ISBT) for pleural and chest wall malignant tumours.

Material and methods: This single-centre retrospective cohort study involved 21 patients with pleural/chest wall malignant tumours treated between January 2024 and January 2025. All patients underwent HDR ISBT (30 Gy in a single fraction). Treatment included CT-guided needle implantation, three-dimensional dose optimisation (Oncentra system), and adherence to Radiation Therapy Oncology Group dose constraints for organs at risk (OARs). Efficacy endpoints included objective response (Response Evaluation Criteria in Solid Tumours v1.1), pain relief (Numerical Rating Scale), and dosimetric comparison with virtual stereotactic body radiotherapy. Safety was assessed using the Radiation Therapy Oncology Group/European Organisation for Research and Treatment of Cancer toxicity criteria.

Results: The median follow-up duration was 7.48 months. The objective response rate (complete response + partial response) was 76.19%, with 28.57% achieving a complete response and 47.62% achieving a partial response. Pain relief was achieved in 87.5% of patients with pretreatment pain, with numerical rating scale scores decreasing from moderate to severe (median, 6) to mild (median, 3) at 1 month. No ≥ grade II complications (e.g. bronchopleural fistula, pneumothorax) occurred; only four patients experienced minor subcutaneous haemorrhage/emphysema. Dosimetric analysis showed a significantly higher target mean dose with ISBT than with stereotactic body radiotherapy (p < 0.001), while OARs doses (e.g. lungs, heart, spinal cord) remained within Radiation Therapy Oncology Group limits. Rib and chest wall dose exceedances were rare and clinically insignificant.

Conclusions: Computed tomography-guided 192Ir HDR ISBT offers safe, effective local control and rapid pain relief for pleural/chest wall tumours, demonstrating superior dosimetric conformity and lower toxicity to OARs. This minimally invasive approach is a viable option for patients unsuitable for surgery or external beam radiotherapy.

Abstract Image

Abstract Image

高剂量-192间质近距离放射治疗胸膜和胸壁肿瘤的安全性和有效性:初步结果。
目的:评价计算机断层扫描(CT)引导下高剂量率(HDR) 192 -铱(192Ir)间质近距离放射治疗胸膜和胸壁恶性肿瘤的安全性和有效性。材料和方法:这项单中心回顾性队列研究纳入了21例在2024年1月至2025年1月间接受治疗的胸膜/胸壁恶性肿瘤患者。所有患者均接受HDR ISBT(单次30 Gy)。治疗包括ct引导下的针头植入,三维剂量优化(Oncentra系统),并遵守放射治疗肿瘤组对危险器官(OARs)的剂量限制。疗效终点包括客观反应(实体肿瘤反应评价标准v1.1)、疼痛缓解(数值评定量表)以及与虚拟立体定向全身放疗的剂量学比较。安全性评估采用放射治疗肿瘤组/欧洲癌症研究和治疗组织的毒性标准。结果:中位随访时间为7.48个月。客观缓解率(完全缓解+部分缓解)为76.19%,其中完全缓解28.57%,部分缓解47.62%。87.5%的预处理疼痛患者实现了疼痛缓解,1个月时,数值评定量表评分从中度到重度(中位数,6)到轻度(中位数,3)下降。未发生≥II级并发症(如支气管胸膜瘘、气胸);只有4例患者出现了轻微的皮下出血/肺气肿。剂量学分析显示,ISBT的靶平均剂量明显高于立体定向放射治疗(p < 0.001),而OARs的剂量(如肺、心脏、脊髓)仍在放射治疗肿瘤学组的限制范围内。肋骨和胸壁的剂量超标是罕见的,临床上不明显。结论:计算机断层扫描引导的192Ir HDR ISBT对胸膜/胸壁肿瘤提供了安全、有效的局部控制和快速疼痛缓解,显示出优越的剂量一致性和对OARs的低毒性。对于不适合手术或外部放射治疗的患者,这种微创方法是一种可行的选择。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Contemporary Brachytherapy
Journal of Contemporary Brachytherapy ONCOLOGY-RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
CiteScore
2.40
自引率
14.30%
发文量
54
审稿时长
16 weeks
期刊介绍: The “Journal of Contemporary Brachytherapy” is an international and multidisciplinary journal that will publish papers of original research as well as reviews of articles. Main subjects of the journal include: clinical brachytherapy, combined modality treatment, advances in radiobiology, hyperthermia and tumour biology, as well as physical aspects relevant to brachytherapy, particularly in the field of imaging, dosimetry and radiation therapy planning. Original contributions will include experimental studies of combined modality treatment, tumor sensitization and normal tissue protection, molecular radiation biology, and clinical investigations of cancer treatment in brachytherapy. Another field of interest will be the educational part of the journal.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信