Bone-only oligometastatic prostate cancer: can SABR improve outcomes? A single-center experience.

IF 1.8 Q3 ONCOLOGY Radiation Oncology Journal Pub Date : 2022-09-01 Epub Date: 2022-09-27 DOI:10.3857/roj.2022.00101
Ángel L Sánchez-Iglesias, Virginia Morillo-Macías, Ana Santafé-Jiménez, Carlos Ferrer-Albiach
{"title":"Bone-only oligometastatic prostate cancer: can SABR improve outcomes? A single-center experience.","authors":"Ángel L Sánchez-Iglesias,&nbsp;Virginia Morillo-Macías,&nbsp;Ana Santafé-Jiménez,&nbsp;Carlos Ferrer-Albiach","doi":"10.3857/roj.2022.00101","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>Ablative treatment of oligometastases has shown survival benefit with certain tumors, although these effects still are to be demonstrated in prostate cancer.</p><p><strong>Materials and methods: </strong>We analysed the toxicity and clinical control results obtained in patients with bone-only oligometastatic prostate cancer treated with stereotactic ablative radiotherapy (SABR). Retrospective study on patients with metachronous oligoprogression and synchronous de novo bone-only oligometastatic prostate cancer treated with SABR and androgen deprivation therapy.</p><p><strong>Results: </strong>Treatment schedules varied according to location and organs at risk, with biologically equivalent dose (BED) ≥100 Gy. Fifty-five bone lesions (31 patients) were treated and evaluated for toxicity, local control, progression-free survival (PFS), and overall survival (OS). After a 41-month follow-up, there was minimal acute or chronic toxicity and no G3 toxicity. The local control at 3 and 5 years was 100% and 87.1%, respectively. Median PFS and OS were 43 and 98 months, respectively. The best result in PFS was obtained with BED ≥230 Gy, delaying time to the next systemic therapy by 28.5 months.</p><p><strong>Conclusion: </strong>The use of SABR in bone oligometastases of prostate cancer is safe with minimal toxicity and excellent results in local control and PFS, delaying the start of the next systemic therapy.</p>","PeriodicalId":46572,"journal":{"name":"Radiation Oncology Journal","volume":"40 3","pages":"192-199"},"PeriodicalIF":1.8000,"publicationDate":"2022-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://ftp.ncbi.nlm.nih.gov/pub/pmc/oa_pdf/85/d7/roj-2022-00101.PMC9535412.pdf","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Radiation Oncology Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3857/roj.2022.00101","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/9/27 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 1

Abstract

Purpose: Ablative treatment of oligometastases has shown survival benefit with certain tumors, although these effects still are to be demonstrated in prostate cancer.

Materials and methods: We analysed the toxicity and clinical control results obtained in patients with bone-only oligometastatic prostate cancer treated with stereotactic ablative radiotherapy (SABR). Retrospective study on patients with metachronous oligoprogression and synchronous de novo bone-only oligometastatic prostate cancer treated with SABR and androgen deprivation therapy.

Results: Treatment schedules varied according to location and organs at risk, with biologically equivalent dose (BED) ≥100 Gy. Fifty-five bone lesions (31 patients) were treated and evaluated for toxicity, local control, progression-free survival (PFS), and overall survival (OS). After a 41-month follow-up, there was minimal acute or chronic toxicity and no G3 toxicity. The local control at 3 and 5 years was 100% and 87.1%, respectively. Median PFS and OS were 43 and 98 months, respectively. The best result in PFS was obtained with BED ≥230 Gy, delaying time to the next systemic therapy by 28.5 months.

Conclusion: The use of SABR in bone oligometastases of prostate cancer is safe with minimal toxicity and excellent results in local control and PFS, delaying the start of the next systemic therapy.

Abstract Image

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
仅骨少转移性前列腺癌:SABR能改善预后吗?单中心体验。
目的:消融治疗寡转移瘤已显示出对某些肿瘤的生存有利,尽管这些作用仍有待于在前列腺癌中得到证实。材料与方法:我们分析了立体定向消融放疗(SABR)治疗仅骨少转移性前列腺癌的毒性和临床对照结果。SABR联合雄激素剥夺治疗异时性少进展和同步新生仅骨少转移性前列腺癌的回顾性研究。结果:治疗方案根据部位和危险器官不同而不同,生物等效剂量(BED)≥100 Gy。对55例(31例)骨病变进行治疗,并评估其毒性、局部控制、无进展生存期(PFS)和总生存期(OS)。随访41个月,急性或慢性毒性最小,无G3毒性。3年和5年局部控制率分别为100%和87.1%。中位PFS和OS分别为43个月和98个月。当BED≥230 Gy时,获得PFS的最佳结果,延迟到下一次全身治疗的时间28.5个月。结论:SABR用于前列腺癌骨少转移是安全的,毒性小,局部控制和PFS效果良好,延迟了下一次全身治疗的开始。
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
3.50
自引率
4.30%
发文量
24
期刊最新文献
Proton beam therapy as a promising option for high-risk limited stage small cell lung cancer: revealing potential of future novel agents Different approaches to target volume definition and boost delivery in surgery de-escalation clinical trial in breast cancer patients with pathological complete response Target movement according to cervical lymph node level in head and neck cancer and its clinical significance Comparison of radiotherapy techniques in patients with thymic epithelial tumor who underwent postoperative radiotherapy Pulmonary function and toxicities of proton versus photon for limited-stage small cell lung cancer
×
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