Androgen Deprivation Therapy Practice Patterns in High-Risk Prostate Cancer Treated With Definitive Radiotherapy: Prospective Results From a Statewide Quality Consortium.

IF 4.6 3区 医学 Q1 ONCOLOGY
Michael P Dykstra, Samuel N Regan, Huiying Maggie Yin, Patrick William McLaughlin, Mark Zaki, Mazen Mislmani, Steven R Miller, Vrinda Narayana, Danielle Kendrick, Murshed Khadija, Daniel Dryden, Dale W Litzenberg, Melissa Mietzel, David K Heimburger, Matthew Schipper, William C Jackson, Robert T Dess
{"title":"Androgen Deprivation Therapy Practice Patterns in High-Risk Prostate Cancer Treated With Definitive Radiotherapy: Prospective Results From a Statewide Quality Consortium.","authors":"Michael P Dykstra, Samuel N Regan, Huiying Maggie Yin, Patrick William McLaughlin, Mark Zaki, Mazen Mislmani, Steven R Miller, Vrinda Narayana, Danielle Kendrick, Murshed Khadija, Daniel Dryden, Dale W Litzenberg, Melissa Mietzel, David K Heimburger, Matthew Schipper, William C Jackson, Robert T Dess","doi":"10.1200/OP-25-00489","DOIUrl":null,"url":null,"abstract":"<p><strong>Purpose: </strong>The 2022 AUA/ASTRO guidelines recommend 18-36 months of androgen deprivation therapy (ADT) with definitive radiotherapy for localized, high-risk prostate cancer. The STAMPEDE M0 trial supports intensification with androgen receptor pathway inhibitors (ARPIs) for patients with ≥2 cT3/T4, Grade Group [GG] 4-5, prostate-specific antigen (PSA) ≥40 ng/mL, or cN1. Given advances in imaging, risk stratification, and treatment delivery, we characterized contemporary practice patterns using prospective data from the Michigan Radiation Oncology Quality Consortium (MROQC).</p><p><strong>Methods: </strong>Patients enrolled in MROQC with intact, high-risk M0/N0-1 prostate cancer were included. Clinical information, including intended ADT duration and ARPI use, was prospectively collected. The primary outcome was intended guideline-concordant ADT (GC-ADT, ≥18 months). Multivariable analyses (MVA) assessed associations between clinical factors and GC-ADT recommendations. We compared the adoption of ARPI with standard therapies before and after the publication of STAMPEDE M0. Facility-level variability was evaluated using a mixed-effects model, with the treatment site as a random intercept.</p><p><strong>Results: </strong>Between June 2020 and November 2024, 553 patients across 26 centers were included: cT3/4 (13.3%), cN1 (19.9%), GG 4-5 (75.0%), and PSA ≥20 ng/mL (40.0%). Overall, 91.3% were recommended ADT, with 67.0% being guideline-concordant. On MVA, GC-ADT was significantly associated with cN1 (odds ratio [OR], 2.94 [95% CI, 1.44 to 5.99]), GG (GG4 OR, 6.23 [95% CI, 2.85 to 13.62]; GG5 OR, 9.45 [95% CI, 4.46 to 20.06]), and PSA ≥40 (OR, 3.64 [95% CI, 1.22-10.87]). Facility-level variability persisted in the MVA (<i>P</i> < .0001). Among the 27.9% who met meeting STAMPEDE criteria, ARPI recommendations increased from 0% prepublication to 23.2% afterward.</p><p><strong>Conclusion: </strong>Within a statewide quality consortium, guideline-concordant ADT recommendations occurred in two thirds of patients, with ARPI intensification in under 25% among STAMPEDE-eligible patients. These findings highlight the need for individualized ADT strategies and collaborative efforts to standardize high-quality care.</p>","PeriodicalId":14612,"journal":{"name":"JCO oncology practice","volume":" ","pages":"OP2500489"},"PeriodicalIF":4.6000,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JCO oncology practice","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1200/OP-25-00489","RegionNum":3,"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

Purpose: The 2022 AUA/ASTRO guidelines recommend 18-36 months of androgen deprivation therapy (ADT) with definitive radiotherapy for localized, high-risk prostate cancer. The STAMPEDE M0 trial supports intensification with androgen receptor pathway inhibitors (ARPIs) for patients with ≥2 cT3/T4, Grade Group [GG] 4-5, prostate-specific antigen (PSA) ≥40 ng/mL, or cN1. Given advances in imaging, risk stratification, and treatment delivery, we characterized contemporary practice patterns using prospective data from the Michigan Radiation Oncology Quality Consortium (MROQC).

Methods: Patients enrolled in MROQC with intact, high-risk M0/N0-1 prostate cancer were included. Clinical information, including intended ADT duration and ARPI use, was prospectively collected. The primary outcome was intended guideline-concordant ADT (GC-ADT, ≥18 months). Multivariable analyses (MVA) assessed associations between clinical factors and GC-ADT recommendations. We compared the adoption of ARPI with standard therapies before and after the publication of STAMPEDE M0. Facility-level variability was evaluated using a mixed-effects model, with the treatment site as a random intercept.

Results: Between June 2020 and November 2024, 553 patients across 26 centers were included: cT3/4 (13.3%), cN1 (19.9%), GG 4-5 (75.0%), and PSA ≥20 ng/mL (40.0%). Overall, 91.3% were recommended ADT, with 67.0% being guideline-concordant. On MVA, GC-ADT was significantly associated with cN1 (odds ratio [OR], 2.94 [95% CI, 1.44 to 5.99]), GG (GG4 OR, 6.23 [95% CI, 2.85 to 13.62]; GG5 OR, 9.45 [95% CI, 4.46 to 20.06]), and PSA ≥40 (OR, 3.64 [95% CI, 1.22-10.87]). Facility-level variability persisted in the MVA (P < .0001). Among the 27.9% who met meeting STAMPEDE criteria, ARPI recommendations increased from 0% prepublication to 23.2% afterward.

Conclusion: Within a statewide quality consortium, guideline-concordant ADT recommendations occurred in two thirds of patients, with ARPI intensification in under 25% among STAMPEDE-eligible patients. These findings highlight the need for individualized ADT strategies and collaborative efforts to standardize high-quality care.

雄激素剥夺疗法在高风险前列腺癌放疗治疗中的实践模式:来自全国质量联盟的前瞻性结果。
目的:2022年AUA/ASTRO指南推荐对局限性高风险前列腺癌进行18-36个月的雄激素剥夺治疗(ADT)加最终放疗。STAMPEDE M0试验支持对≥2 cT3/T4、分级组[GG] 4-5、前列腺特异性抗原(PSA)≥40 ng/mL或cN1的患者使用雄激素受体途径抑制剂(arpi)进行强化治疗。鉴于影像学、风险分层和治疗方式的进步,我们利用密歇根放射肿瘤学质量联盟(MROQC)的前瞻性数据对当代实践模式进行了描述。方法:纳入MROQC的完整、高风险M0/N0-1前列腺癌患者。前瞻性收集临床信息,包括预期ADT持续时间和ARPI使用情况。主要终点为指南一致性ADT (GC-ADT,≥18个月)。多变量分析(MVA)评估了临床因素与GC-ADT推荐值之间的关系。我们比较了STAMPEDE M0发表前后采用ARPI与标准疗法的情况。使用混合效应模型评估设施水平的可变性,治疗地点作为随机截距。结果:2020年6月至2024年11月,纳入26个中心的553例患者:cT3/4 (13.3%), cN1 (19.9%), GG 4-5 (75.0%), PSA≥20 ng/mL(40.0%)。总体而言,91.3%推荐ADT, 67.0%与指南一致。在MVA中,GC-ADT与cN1(比值比[OR], 2.94 [95% CI, 1.44 ~ 5.99])、GG (GG4 OR, 6.23 [95% CI, 2.85 ~ 13.62]; GG5 OR, 9.45 [95% CI, 4.46 ~ 20.06])和PSA≥40 (OR, 3.64 [95% CI, 1.22 ~ 10.87])显著相关。设施水平的可变性在MVA中持续存在(P < 0.0001)。在27.9%符合STAMPEDE标准的患者中,ARPI推荐率从发表前的0%上升到发表后的23.2%。结论:在全州范围内的质量联盟中,三分之二的患者推荐符合指南的ADT,在符合stampede的患者中,ARPI强化发生率低于25%。这些发现强调了个性化ADT策略和协作努力标准化高质量护理的必要性。
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
6.40
自引率
7.50%
发文量
518
×
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