Santoni Matteo, Büttner Thomas, Rescigno Pasquale, Fiala Ondrej, Cavasin Nicolò, Basso Umberto, Taha Tarek, Massari Francesco, Myint Zin W, Formisano Luigi, Galli Luca, Scagliarini Sarah, Matrana Marc R, Facchini Gaetano, Bamias Aristotelis, Messina Carlo, Zacchi Francesca, Manneh Ray Kopp, Roviello Giandomenico, Santini Daniele, Poprach Alexandr, Navratil Jiri, Uher Michal, Calabrò Fabio, Pierce Erin, Berardi Rossana, Aurilio Gaetano, Zakopoulou Roubini, Rizzo Alessandro, Ansari Jawaher, Rizzo Mimma, Bisonni Renato, Mollica Veronica, Incorvaia Lorena, Spinelli Gianpaolo, Jiang Xue Yan, Chandler Robert Adam, Grillone Francesco, Morelli Franco, Buti Sebastiano, Maluf Fernando C, Marques Monteiro Fernando Sabino, Battelli Nicola, Porta Camillo, Caffo Orazio, Soares Andrey
Medical Oncology Unit, Macerata Hospital, Macerata, Italy.
Department of Urology, University Hospital Bonn, Bonn, Germany.
Eur Urol Oncol. 2025 Apr;8(2):444-451. doi: 10.1016/j.euo.2024.11.005. Epub 2024 Nov 29.
Apalutamide (APA) is a treatment for metastatic castration-sensitive prostate cancer (mCSPC). In the ARON-3 study we investigated real-world experiences with APA treatment for mCSPC.
We retrospectively assessed real-world clinical outcomes for patients with mCSPC treated with APA in the ARON-3 study. Overall survival (OS) was calculated from APA initiation to death from any cause. PSA was defined as a prostate-specific antigen decline of ≥90% from baseline, and PSA as achievement of a PSA level ≤0.2 ng/ml. Data for adverse events were retrospectively collected from electronic and paper charts and categorized according to Common Terminology Criteria for Adverse Events v5.0.
We included 531 patients with mCSPC treated with APA. High-volume disease was reported for 214 patients (40%), and 56 (11%) had visceral metastases. Median OS was not reached. PSA was experienced by 461 patients (87%) and PSA by 368 (69%). Median OS was significantly longer for patients with PSA or PSA than for subjects without these responses (p < 0.001). The incidence of grade 3-4 fatigue was higher among elderly patients (≥80 yr) than among younger patients (19% vs 5%), but the incidence of other adverse events was comparable between the age groups.
APA is an effective and tolerable treatment for mCSPC in the real-world setting.
The ARON-3 project collects data for patients with prostate cancer treated in multiple centers worldwide to assess outcomes in the real-world setting. We analyzed data for patients with metastatic hormone-sensitive prostate cancer receiving apalutamide. Our results show that apalutamide is a safe and effective drug in the real-world setting as well as in clinical trials.
阿帕他胺(APA)是一种用于转移性去势敏感性前列腺癌(mCSPC)的治疗药物。在ARON - 3研究中,我们调查了APA治疗mCSPC的真实世界经验。
我们回顾性评估了ARON - 3研究中接受APA治疗的mCSPC患者的真实世界临床结局。总生存期(OS)从开始使用APA计算至因任何原因死亡。PSA定义为前列腺特异性抗原从基线下降≥90%,而PSA定义为达到PSA水平≤0.2 ng/ml。不良事件数据通过回顾性收集电子和纸质病历,并根据《不良事件通用术语标准》第5.0版进行分类。
我们纳入了531例接受APA治疗的mCSPC患者。214例患者(40%)报告有高负荷疾病,56例(11%)有内脏转移。未达到中位总生存期。461例患者(87%)出现PSA,368例(69%)出现PSA。有PSA或PSA的患者中位总生存期显著长于无这些反应的患者(p < 0.001)。老年患者(≥80岁)3 - 4级疲劳的发生率高于年轻患者(19%对5%),但其他不良事件的发生率在各年龄组之间相当。
在真实世界环境中,APA是一种治疗mCSPC有效且耐受性良好的药物。
ARON - 3项目收集全球多个中心接受治疗的前列腺癌患者的数据,以评估真实世界环境中的结局。我们分析了接受阿帕他胺治疗的转移性激素敏感性前列腺癌患者的数据。我们的结果表明,阿帕他胺在真实世界环境以及临床试验中都是一种安全有效的药物。