Real-World Evidence of Combination Therapy Use in Metastatic Hormone-Sensitive Prostate Cancer in the United States From 2017 to 2023.

IF 4.7 3区 医学 Q1 ONCOLOGY
Amit D Raval, Orsolya Lunacsek, Matthew J Korn, Natasha Littleton, Niculae Constantinovici, Daniel J George
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Abstract

Purpose: Treatment of metastatic hormone-sensitive prostate cancer (mHSPC) has evolved with robust clinical trial evidence on the benefits of combining androgen-deprivation therapy (ADT) with androgen receptor pathway inhibitors (ARPIs; abiraterone, apalutamide, darolutamide, and enzalutamide) and/or docetaxel (DOC). To understand current treatment approaches in clinical practice, we examined combined therapy for mHSPC in US real-world practice.

Methods: This retrospective study used administrative claims in the Komodo Research Dataset (January 2016-September 2023). Individuals with mHSPC were identified on the basis of their earliest claim for metastasis on/after prostate cancer diagnosis date without evidence of castration resistance. Index date was the earliest ADT claim after mHSPC. Combination therapy included the addition of ARPI, DOC, or both to ADT within 4 months of index date. Multinomial regression was used to examine factors associated with combination therapy.

Results: Study population consisted of 10,717 individuals, with a median age of 65 years and a majority of de novo mHSPC cases at diagnosis (62%). Overall, 28% received combination therapy with ARPI (18% abiraterone; 10% apalutamide, darolutamide, or enzalutamide), 9% with DOC, and 2.5% with ARPI plus DOC. From 2017 to 2023, combined hormonal therapy with ARPI increased from 13% to 47% and with ARPI plus DOC from 0.8% to 15%, whereas use of ADT plus DOC declined from 12% to 3% and ADT alone from 74% to 36%. Key factors associated with combination therapy were younger age, fewer chronic comorbidities, de novo mHSPC, and bone metastases.

Conclusion: Although one third of men received ADT alone in 2023, the use of combination hormonal therapy with ARPI and/or DOC increased between 2017 and 2023, highlighting uptake of guideline-recommended treatment, driven by available clinical evidence, disease burden, and tolerability.

2017年至2023年美国转移性激素敏感前列腺癌联合治疗的真实世界证据
目的:转移性激素敏感性前列腺癌(mHSPC)的治疗已经有了强有力的临床试验证据,证明雄激素剥夺疗法(ADT)联合雄激素受体途径抑制剂(arpi)的益处;阿比特龙、阿帕鲁胺、darolutamide和恩杂鲁胺)和/或多西他赛(DOC)。为了了解目前临床实践中的治疗方法,我们在美国的实际实践中研究了mHSPC的联合治疗。方法:本回顾性研究使用了科莫多研究数据集中的行政索赔(2016年1月- 2023年9月)。mHSPC个体是根据他们在前列腺癌诊断当日或之后最早声称转移而没有去势抵抗的证据来确定的。索引日期是mHSPC之后最早的ADT索赔。联合治疗包括在索引日期后4个月内在ADT中添加ARPI、DOC或两者。使用多项回归来检查与联合治疗相关的因素。结果:研究人群包括10,717人,中位年龄为65岁,大多数诊断时为新发mHSPC病例(62%)。总体而言,28%的患者接受了ARPI联合治疗(18%阿比特龙;10%阿帕鲁胺,达罗卢胺,或恩杂鲁胺),9%与DOC, 2.5%与ARPI加DOC。从2017年到2023年,激素联合ARPI治疗从13%增加到47%,ARPI加DOC从0.8%增加到15%,而ADT加DOC的使用从12%下降到3%,ADT单独使用从74%下降到36%。与联合治疗相关的关键因素是年龄较小、慢性合并症较少、新发mHSPC和骨转移。结论:尽管在2023年有三分之一的男性单独接受ADT治疗,但在2017年至2023年期间,激素联合ARPI和/或DOC治疗的使用有所增加,这表明在现有临床证据、疾病负担和耐受性的推动下,指南推荐治疗的接受程度有所提高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.40
自引率
7.50%
发文量
518
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