Combined Fixed-duration Systemic Treatment and Metastasis-directed Radiotherapy for Oligometastatic Hormone-sensitive Prostate Cancer.

IF 8.3 1区 医学 Q1 ONCOLOGY
Praful Ravi, Caiwei Zhong, Wanling Xie, Emma Kelly, Bridget Whelpley, Katelyn Kuczmarski, Himisha Beltran, Kerry L Kilbridge, Martin T King, Bradley A McGregor, Alicia K Morgans, Mark Pomerantz, Mary-Ellen Taplin, Alok K Tewari, Srinivas R Viswanathan, Xiao X Wei, Mai Anh Huynh, Atish D Choudhury
{"title":"Combined Fixed-duration Systemic Treatment and Metastasis-directed Radiotherapy for Oligometastatic Hormone-sensitive Prostate Cancer.","authors":"Praful Ravi, Caiwei Zhong, Wanling Xie, Emma Kelly, Bridget Whelpley, Katelyn Kuczmarski, Himisha Beltran, Kerry L Kilbridge, Martin T King, Bradley A McGregor, Alicia K Morgans, Mark Pomerantz, Mary-Ellen Taplin, Alok K Tewari, Srinivas R Viswanathan, Xiao X Wei, Mai Anh Huynh, Atish D Choudhury","doi":"10.1016/j.euo.2024.10.014","DOIUrl":null,"url":null,"abstract":"<p><strong>Background and objective: </strong>It is unclear whether \"total therapy\" (androgen deprivation therapy [ADT] with or without an androgen receptor pathway inhibitor [ARPI], metastasis-directed therapy, and local therapy to the prostate if de novo) may lead to long-term durable remission in oligometastatic hormone-sensitive prostate cancer (omHSPC). This study aims to evaluate the outcomes after the completion of total therapy in patients with omHSPC.</p><p><strong>Methods: </strong>A retrospective single-institution cohort of consecutive patients with omHSPC identified on conventional or molecular imaging treated with total therapy was assembled. All patients had prostate-specific antigen ≤0.1 ng/ml at the completion of systemic therapy. Kaplan-Meier and Cox regression models were used to evaluate the key outcomes of interest: clinical progression-free survival (cPFS), eugonadal progression-free survival (PFS), and time to restart of ADT (TTrADT).</p><p><strong>Key findings and limitations: </strong>Eighty-nine patients were included, of whom 23 were with de novo omHSPC; the median number of metastases was 1, and detection of disease by molecular imaging was performed in 43 patients (48%). Forty-nine patients (55%) received ADT + ARPI doublet and 40 (45%) received ADT alone. At a median follow-up of 37 mo, there were 46 cPFS events; 3-yr cPFS rate was 45% (95% confidence interval 33-56) and the median eugonadal PFS was 12 mo. The median TTrADT was 47 mo, and 60% had not restarted ADT at 3 yr. Duration of systemic therapy ≥12 mo was the only significant predictor of better outcomes.</p><p><strong>Conclusions and clinical implications: </strong>Of the patients receiving total therapy for omHSPC, 45% remained progression free at 3 yr after completing therapy, hinting at the potential for long-term remission and possible cure with this strategy in a subset of patients with omHSPC. Prospective trials evaluating this approach are needed.</p><p><strong>Patient summary: </strong>In this report, we looked at outcomes in men who had received a fixed duration of hormonal therapy along with radiotherapy to metastatic sites (and prostate radiotherapy or surgery in those with newly diagnosed disease) for oligometastatic prostate cancer. We found that nearly half of the patients had no evidence of cancer recurrence at 3 yr after completing therapy, and 60% had not resumed any therapy at this time point.</p>","PeriodicalId":12256,"journal":{"name":"European urology oncology","volume":" ","pages":""},"PeriodicalIF":8.3000,"publicationDate":"2024-11-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"European urology oncology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1016/j.euo.2024.10.014","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"ONCOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Background and objective: It is unclear whether "total therapy" (androgen deprivation therapy [ADT] with or without an androgen receptor pathway inhibitor [ARPI], metastasis-directed therapy, and local therapy to the prostate if de novo) may lead to long-term durable remission in oligometastatic hormone-sensitive prostate cancer (omHSPC). This study aims to evaluate the outcomes after the completion of total therapy in patients with omHSPC.

Methods: A retrospective single-institution cohort of consecutive patients with omHSPC identified on conventional or molecular imaging treated with total therapy was assembled. All patients had prostate-specific antigen ≤0.1 ng/ml at the completion of systemic therapy. Kaplan-Meier and Cox regression models were used to evaluate the key outcomes of interest: clinical progression-free survival (cPFS), eugonadal progression-free survival (PFS), and time to restart of ADT (TTrADT).

Key findings and limitations: Eighty-nine patients were included, of whom 23 were with de novo omHSPC; the median number of metastases was 1, and detection of disease by molecular imaging was performed in 43 patients (48%). Forty-nine patients (55%) received ADT + ARPI doublet and 40 (45%) received ADT alone. At a median follow-up of 37 mo, there were 46 cPFS events; 3-yr cPFS rate was 45% (95% confidence interval 33-56) and the median eugonadal PFS was 12 mo. The median TTrADT was 47 mo, and 60% had not restarted ADT at 3 yr. Duration of systemic therapy ≥12 mo was the only significant predictor of better outcomes.

Conclusions and clinical implications: Of the patients receiving total therapy for omHSPC, 45% remained progression free at 3 yr after completing therapy, hinting at the potential for long-term remission and possible cure with this strategy in a subset of patients with omHSPC. Prospective trials evaluating this approach are needed.

Patient summary: In this report, we looked at outcomes in men who had received a fixed duration of hormonal therapy along with radiotherapy to metastatic sites (and prostate radiotherapy or surgery in those with newly diagnosed disease) for oligometastatic prostate cancer. We found that nearly half of the patients had no evidence of cancer recurrence at 3 yr after completing therapy, and 60% had not resumed any therapy at this time point.

针对寡转移性激素敏感性前列腺癌的固定疗程全身治疗和转移灶定向放疗联合疗法。
背景和目的:目前尚不清楚 "综合治疗"(使用或不使用雄激素受体通路抑制剂[ARPI]的雄激素剥夺疗法[ADT]、转移灶导向疗法和新发前列腺局部疗法)是否能使寡转移性激素敏感性前列腺癌(omHSPC)获得长期持久的缓解。本研究旨在评估omHSPC患者完成整体治疗后的疗效:方法:研究人员对在常规或分子影像学检查中发现的接受整体治疗的连续omHSPC患者进行了回顾性单机构队列分析。所有患者在完成系统治疗时前列腺特异性抗原均≤0.1 ng/ml。采用卡普兰-梅耶(Kaplan-Meier)和考克斯回归模型评估主要的相关结果:临床无进展生存期(cPFS)、优生无进展生存期(PFS)和重新开始 ADT 的时间(TTrADT):共纳入89例患者,其中23例为新发omHSPC;转移灶的中位数为1个,43例患者(48%)通过分子影像学检查发现了疾病。49名患者(55%)接受了ADT+ARPI双联疗法,40名患者(45%)仅接受了ADT疗法。中位随访时间为 37 个月,有 46 例 cPFS 事件;3 年 cPFS 率为 45%(95% 置信区间为 33-56),中位优生 PFS 为 12 个月。中位TTrADT为47个月,60%的患者在3年后未重新开始ADT,系统治疗持续时间≥12个月是唯一显著预测较好结果的因素:在接受omHSPC整体治疗的患者中,45%的患者在完成治疗3年后仍未出现病情进展,这表明在一部分omHSPC患者中,采用这种策略有可能获得长期缓解和治愈。患者摘要:在这份报告中,我们研究了接受固定时间的激素治疗并对转移部位进行放疗(对新确诊的患者进行前列腺放疗或手术)的男性少转移性前列腺癌患者的治疗效果。我们发现,近一半的患者在完成治疗 3 年后没有癌症复发的迹象,60% 的患者在这个时间点没有恢复任何治疗。
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
CiteScore
15.50
自引率
2.40%
发文量
128
审稿时长
20 days
期刊介绍: Journal Name: European Urology Oncology Affiliation: Official Journal of the European Association of Urology Focus: First official publication of the EAU fully devoted to the study of genitourinary malignancies Aims to deliver high-quality research Content: Includes original articles, opinion piece editorials, and invited reviews Covers clinical, basic, and translational research Publication Frequency: Six times a year in electronic format
×
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:481959085
Book学术官方微信