Single and multitarget stereotactic radiosurgery (SRS) with single isocenter in the treatment of multiple brain metastases (BM): institutional experience.

IF 2.8 3区 医学 Q2 ONCOLOGY Clinical & Translational Oncology Pub Date : 2025-01-15 DOI:10.1007/s12094-024-03844-3
Raquel Ciérvide, Jaime Martí, Mercedes López, Ovidio Hernando, Alejandro Prado, Leyre Alonso, Ángel Montero, Beatriz Álvarez, Miguel Angel de la Casa, Daniel Zucca, Ana Ortiz de Mendivil, Patricia Martín, Ana Martínez, Mariola García-Aranda, Emilio Sánchez, Jeannette Valero, Juan García, Xin Chen-Zhao, Rosa Alonso, Pedro Fernandez-Leton, Carmen Rubio
{"title":"Single and multitarget stereotactic radiosurgery (SRS) with single isocenter in the treatment of multiple brain metastases (BM): institutional experience.","authors":"Raquel Ciérvide, Jaime Martí, Mercedes López, Ovidio Hernando, Alejandro Prado, Leyre Alonso, Ángel Montero, Beatriz Álvarez, Miguel Angel de la Casa, Daniel Zucca, Ana Ortiz de Mendivil, Patricia Martín, Ana Martínez, Mariola García-Aranda, Emilio Sánchez, Jeannette Valero, Juan García, Xin Chen-Zhao, Rosa Alonso, Pedro Fernandez-Leton, Carmen Rubio","doi":"10.1007/s12094-024-03844-3","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>SRS for the treatment of limited brain metastases (BM) is widely accepted, but there are still limitations in the management of numerous BM. Frameless single-isocenter multitarget SRS is a novel technique that allows for rapid treatment delivery to multiple BM. We report our preliminary clinical, dosimetric, and patient´s shifts outcomes with this technique.</p><p><strong>Materials and methods: </strong>We have reviewed clinical and dosimetric outcomes of patients with intact BM treated with SRS using one isocenter either for single (1BM) or multiple (≥ 2BM) targets). Immobilization was based on an SRS stereotactic mask. Elements Multiple Brain Mets SRS (Brainlab AG, Munich, Germany) software was used for registration, image fusion, target contouring, and treatment planning. Exactrac Dynamic (Brainlab AG, Munich, Germany) and a 6 degree of freedom couch were used for monitoring, correcting the position and assessing and applying residual errors also when couch rotations. During dose delivery, the patient position was monitored and registered using surface tracking and stereoscopic X-rays.</p><p><strong>Results: </strong>From May 2022 to December 2023, we treated 60 patients with a total of 255 BM. The 67% of patients had at least 2 BM treated and the average of treated BM per patient per course was 3.6 (range 1-13). The average total treated BM per patient (sum of all courses) was 4.4. Lung cancer was the most frequent (63%) primary tumor. 77% of cases were patients with a brain relapse and the remaining 23% had BM at diagnosis. Ninety-two percent of BM were treated with single fraction. The most used fractionations were 20 Gy (27.8%) and 21 Gy (43.5%), respectively, and the median PTV target volume (if single fraction) was 0,2 cc (range 0.016-4.32 cc). The median cumulative target volume per isocenter and the sum of all SRS courses were 1.37 and 1.46 cc, respectively. The 100% of patients completed the SRS treatment with no incidences. With an average follow-up of 8.3 months (0.1-19 months), we have not identified any local relapse, although 27% developed an intracranial relapse that was again treated with SRS in the 44% of cases. We did not find any relation between overall survival and the presence of any driver mutation (p = 0.97), presence of BM at diagnosis vs. recurrences (p = 0.113), number of courses of SRS (p = 0.688), number of isocenters (p = 0.679), or number of treated BM (1 vs. 2-3 vs. ≥ 4; p = 0.7). Healthy normal tissue constraints were adequately accomplished with a median V12 (if single dose) and V20 (if 5 fractions) of 0.2 and 5 cc, respectively. No acute toxicity > G2 was reported. Regarding patient positioning, monitoring, and registration based on X-ray imaging and surface guidance, patient shifts distributions were centered at 0.0 mm with standard deviations below 0.25 mm, except for the longitudinal shift based on X-rays, which was 0.35 mm. This implies an adequate fixation system, patient setup, and image guidance protocols. The mean total delivery time per fraction, from the first beam-on to the last beam-off, was 9.6 ± 4.8 min, with a range of 4.6-30.9 min. On average, repositioning occurred 1.2 times per fraction based on X-ray guidance and 0.6 times per fraction based on surface guidance.</p><p><strong>Conclusion: </strong>Based on our preliminary experience, we find single isocenter for single and multitarget SRS technique is feasible, well tolerated and allows excellent local control. Regarding patient positioning, monitoring, and registration based on X-ray imaging and surface guidance, patients' shifts and repositioning rate are low enough to show an adequate fixation system, patient setup, and image guidance policies at our institution. Patient shifts during treatment are effectively managed by X-ray and SGRT verification. Low shift tolerances ensure patient stability, resulting in acceptable treatment times and patient repositioning rates. This dedicated workflow for SRS at our institution demonstrates excellent clinical outcomes. A longer follow-up period is necessary to evaluate the impact on long-term clinical outcomes.</p>","PeriodicalId":50685,"journal":{"name":"Clinical & Translational Oncology","volume":" ","pages":""},"PeriodicalIF":2.8000,"publicationDate":"2025-01-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Clinical & Translational Oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1007/s12094-024-03844-3","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: SRS for the treatment of limited brain metastases (BM) is widely accepted, but there are still limitations in the management of numerous BM. Frameless single-isocenter multitarget SRS is a novel technique that allows for rapid treatment delivery to multiple BM. We report our preliminary clinical, dosimetric, and patient´s shifts outcomes with this technique.

Materials and methods: We have reviewed clinical and dosimetric outcomes of patients with intact BM treated with SRS using one isocenter either for single (1BM) or multiple (≥ 2BM) targets). Immobilization was based on an SRS stereotactic mask. Elements Multiple Brain Mets SRS (Brainlab AG, Munich, Germany) software was used for registration, image fusion, target contouring, and treatment planning. Exactrac Dynamic (Brainlab AG, Munich, Germany) and a 6 degree of freedom couch were used for monitoring, correcting the position and assessing and applying residual errors also when couch rotations. During dose delivery, the patient position was monitored and registered using surface tracking and stereoscopic X-rays.

Results: From May 2022 to December 2023, we treated 60 patients with a total of 255 BM. The 67% of patients had at least 2 BM treated and the average of treated BM per patient per course was 3.6 (range 1-13). The average total treated BM per patient (sum of all courses) was 4.4. Lung cancer was the most frequent (63%) primary tumor. 77% of cases were patients with a brain relapse and the remaining 23% had BM at diagnosis. Ninety-two percent of BM were treated with single fraction. The most used fractionations were 20 Gy (27.8%) and 21 Gy (43.5%), respectively, and the median PTV target volume (if single fraction) was 0,2 cc (range 0.016-4.32 cc). The median cumulative target volume per isocenter and the sum of all SRS courses were 1.37 and 1.46 cc, respectively. The 100% of patients completed the SRS treatment with no incidences. With an average follow-up of 8.3 months (0.1-19 months), we have not identified any local relapse, although 27% developed an intracranial relapse that was again treated with SRS in the 44% of cases. We did not find any relation between overall survival and the presence of any driver mutation (p = 0.97), presence of BM at diagnosis vs. recurrences (p = 0.113), number of courses of SRS (p = 0.688), number of isocenters (p = 0.679), or number of treated BM (1 vs. 2-3 vs. ≥ 4; p = 0.7). Healthy normal tissue constraints were adequately accomplished with a median V12 (if single dose) and V20 (if 5 fractions) of 0.2 and 5 cc, respectively. No acute toxicity > G2 was reported. Regarding patient positioning, monitoring, and registration based on X-ray imaging and surface guidance, patient shifts distributions were centered at 0.0 mm with standard deviations below 0.25 mm, except for the longitudinal shift based on X-rays, which was 0.35 mm. This implies an adequate fixation system, patient setup, and image guidance protocols. The mean total delivery time per fraction, from the first beam-on to the last beam-off, was 9.6 ± 4.8 min, with a range of 4.6-30.9 min. On average, repositioning occurred 1.2 times per fraction based on X-ray guidance and 0.6 times per fraction based on surface guidance.

Conclusion: Based on our preliminary experience, we find single isocenter for single and multitarget SRS technique is feasible, well tolerated and allows excellent local control. Regarding patient positioning, monitoring, and registration based on X-ray imaging and surface guidance, patients' shifts and repositioning rate are low enough to show an adequate fixation system, patient setup, and image guidance policies at our institution. Patient shifts during treatment are effectively managed by X-ray and SGRT verification. Low shift tolerances ensure patient stability, resulting in acceptable treatment times and patient repositioning rates. This dedicated workflow for SRS at our institution demonstrates excellent clinical outcomes. A longer follow-up period is necessary to evaluate the impact on long-term clinical outcomes.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
单等中心单靶点和多靶点立体定向放射手术(SRS)治疗多发性脑转移瘤(BM):机构经验。
SRS治疗局限性脑转移瘤(BM)已被广泛接受,但在大量脑转移瘤的治疗中仍存在局限性。无框单等中心多靶点SRS是一种新的技术,可以快速治疗多个脑转移。我们报告了我们的初步临床,剂量学和患者转移结果与该技术。材料和方法:我们回顾了完整脑脊膜炎患者使用一个等中心SRS治疗单个(1BM)或多个(≥2BM)靶点的临床和剂量学结果。固定基于SRS立体定向面罩。Elements Multiple Brain Mets SRS (Brainlab AG, Munich, Germany)软件用于配准、图像融合、目标轮廓和治疗计划。使用Exactrac Dynamic (Brainlab AG, Munich, Germany)和一个6自由度沙发来监测、校正位置,并在沙发旋转时评估和应用残余误差。在给药过程中,使用表面跟踪和立体x射线监测和记录患者的位置。结果:从2022年5月到2023年12月,我们治疗了60例患者,共255例BM。67%的患者至少接受了2例脑转移治疗,每名患者每疗程平均接受3.6例脑转移治疗(范围1-13)。每位患者的平均总治疗BM(所有疗程的总和)为4.4。肺癌是最常见的原发肿瘤(63%)。77%的病例为脑复发患者,其余23%在诊断时为脑转移。92%的脑脊膜炎采用单组分治疗。最常用的馏分分别为20 Gy(27.8%)和21 Gy (43.5%), PTV靶体积中位数(如果是单一馏分)为0,2 cc(范围为0.016-4.32 cc)。每个等中心的中位累积靶体积和所有SRS疗程的总和分别为1.37和1.46 cc。100%的患者完成了SRS治疗,无并发症发生。平均随访8.3个月(0.1-19个月),我们没有发现任何局部复发,尽管27%的病例出现颅内复发,44%的病例再次接受SRS治疗。我们没有发现总生存率与任何驱动突变的存在(p = 0.97)、诊断时BM的存在与复发(p = 0.113)、SRS病程数(p = 0.688)、等中心数(p = 0.679)或治疗BM的数量(1 vs. 2-3 vs.≥4;p = 0.7)。健康正常组织约束的中位V12(单次剂量)和V20(5次剂量)分别为0.2和5cc。无急性毒性> G2报告。在基于x射线成像和表面引导的患者定位、监测和登记方面,除了基于x射线的纵向移位为0.35 mm外,患者移位分布集中在0.0 mm,标准差小于0.25 mm。这意味着一个适当的固定系统、病人设置和图像引导方案。从第一束射入到最后一束射入,每个射入段的平均总发射时间为9.6±4.8 min,范围为4.6-30.9 min。基于x射线制导的每个射入段平均重新定位1.2次,基于表面制导的每个射入段平均重新定位0.6次。结论:基于我们的初步经验,我们发现单和多靶点SRS技术是可行的,耐受性好,具有良好的局部控制性。关于基于x射线成像和表面引导的患者定位、监测和登记,患者的移位和重新定位率足够低,表明我们机构有足够的固定系统、患者设置和图像引导政策。通过x射线和SGRT验证有效地管理治疗期间的患者轮班。低位移容限确保患者稳定性,导致可接受的治疗时间和患者重新定位率。我们机构的SRS专用工作流程显示出良好的临床效果。需要更长的随访期来评估对长期临床结果的影响。
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 去求助
来源期刊
CiteScore
6.20
自引率
2.90%
发文量
240
审稿时长
1 months
期刊介绍: Clinical and Translational Oncology is an international journal devoted to fostering interaction between experimental and clinical oncology. It covers all aspects of research on cancer, from the more basic discoveries dealing with both cell and molecular biology of tumour cells, to the most advanced clinical assays of conventional and new drugs. In addition, the journal has a strong commitment to facilitating the transfer of knowledge from the basic laboratory to the clinical practice, with the publication of educational series devoted to closing the gap between molecular and clinical oncologists. Molecular biology of tumours, identification of new targets for cancer therapy, and new technologies for research and treatment of cancer are the major themes covered by the educational series. Full research articles on a broad spectrum of subjects, including the molecular and cellular bases of disease, aetiology, pathophysiology, pathology, epidemiology, clinical features, and the diagnosis, prognosis and treatment of cancer, will be considered for publication.
期刊最新文献
Azathioprine and risk of non-melanoma skin cancers in organ transplant recipients: a systematic review and update meta-analysis. PMN-MDSCs are responsible for immune suppression in anti-PD-1 treated TAP1 defective melanoma. Gender and sex differences in colorectal cancer screening, diagnosis and treatment. Evaluating the prognostic role of glucose-to-lymphocyte ratio in patients with metastatic renal cell carcinoma treated with tyrosine kinase inhibitors in first line: a study by the Turkish Oncology Group Kidney Cancer Consortium (TKCC). Single and multitarget stereotactic radiosurgery (SRS) with single isocenter in the treatment of multiple brain metastases (BM): institutional experience.
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1