Treatment Trajectories in Metastatic Hormone-sensitive Prostate Cancer: A PIONEER+ Big Data Analysis.

IF 9.3 1区 医学 Q1 ONCOLOGY
Rossella Nicoletti, Alex Qinyang Liu, Susan Evans-Axelsson, Asieh Golozar, Katharina Beyer, Bertrand De Meulder, Riccardo Campi, Mauro Gacci, Jeremy Yuen-Chun Teoh, Carl Steinbesser, Ayman Hijazy, Artem Harbachou, James T Brash, Peter-Paul M Willemse, Teemu Murtola, Monique J Roobol, Jesus Moreno Sierra, Anders Bjartell, Axel S Merseburger, Pawel Rajwa, Philip Cornford, Thomas Abbott, James Ndow, Juan Gomez Rivas, Eleanor Davies, Qi Feng, Robert Snijder
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Abstract

Background and objective: The treatment landscape for metastatic hormone-sensitive prostate cancer (mHSPC) is evolving rapidly. Real-world data (RWD) are essential to understand actual treatment use and outcomes. This study aimed to describe treatment trajectories and clinical outcomes in a large, multicenter RWD cohort under the PIONEER project.

Methods: Eight European and US databases (2016-2020), including electronic health records, insurance claims, primary care data, and cancer registries, were standardized to the Observational Medical Outcome Partnership Common Data Model. Patients diagnosed with mHSPC and those receiving treatment were identified. The compared and analyzed outcomes included treatment switch, symptomatic progression, adverse events, and death.

Key findings and limitations: In total, 107 438 patients with mHSPC were identified, and 67 909 received treatment. Most of the patients received androgen deprivation therapy (ADT) monotherapy (69.4%), followed by ADT + an androgen receptor pathway inhibitor (ARPI; 15.2%), ADT + chemotherapy (14.0%), and triplet therapy (1.2%). The use of ARPIs increased over time. ADT + ARPI showed the highest persistence (53.8%) and a 5-yr switch-free survival rate of up to 72.3%. ADT monotherapy had 5-yr switch-free survival rates of 21.3-58.6% and adverse event-free survival rates of 64.7-81.2%. Addition of an ARPI improved switch-free survival (24.1-72.3%) but lowered adverse event-free survival (55.2-82.7%). Chemotherapy-based and triplet therapies showed variable results without consistent survival benefit. Limitations include residual confounding, inconsistent adverse event reporting, and possible data overlap.

Conclusions and clinical implications: This is the largest RWD study of systemic mHSPC treatment. Despite evidence, ADT monotherapy remains the most used first-line therapy. Increased use ADT + ARPI is associated with better persistence and improved outcomes in the real-world setting, supporting its broader adoption in clinical practice.

转移性激素敏感前列腺癌的治疗轨迹:先锋+大数据分析。
背景和目的:转移性激素敏感性前列腺癌(mHSPC)的治疗前景正在迅速发展。真实世界数据(RWD)对于了解实际治疗使用和结果至关重要。本研究旨在描述PIONEER项目下大型多中心RWD队列的治疗轨迹和临床结果。方法:8个欧洲和美国数据库(2016-2020),包括电子健康记录、保险索赔、初级保健数据和癌症登记,标准化为观察性医疗结局伙伴关系公共数据模型。确定诊断为mHSPC的患者和接受治疗的患者。比较和分析的结果包括治疗转换、症状进展、不良事件和死亡。主要发现和局限性:共有107 438例mHSPC患者被确定,67 909例接受了治疗。大多数患者接受雄激素剥夺治疗(ADT)单药治疗(69.4%),其次是ADT +雄激素受体途径抑制剂(ARPI; 15.2%)、ADT +化疗(14.0%)和三联治疗(1.2%)。arpi的使用随着时间的推移而增加。ADT + ARPI表现出最高的持久性(53.8%),5年无切换生存率高达72.3%。ADT单药治疗的5年无切换生存率为21.3-58.6%,无不良事件生存率为64.7-81.2%。ARPI的增加提高了无开关生存率(24.1-72.3%),但降低了无不良事件生存率(55.2-82.7%)。基于化疗和三联疗法显示出不同的结果,没有一致的生存益处。局限性包括残留混淆、不良事件报告不一致和可能的数据重叠。结论和临床意义:这是系统性mHSPC治疗的最大RWD研究。尽管有证据表明,ADT单药治疗仍然是最常用的一线治疗。增加ADT + ARPI的使用与现实环境中更好的持久性和改善的结果相关,支持其在临床实践中的广泛采用。
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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
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