Apalutamide in Metastatic Castration-sensitive Prostate Cancer: Results from the Multicenter Real-world ARON-3 Study

ARON-3 is an international, multicenter, retrospective study to collect global experiences in the treatment of patients with advanced prostate cancer. Our results confirm the safety, tolerability, and efficacy of apalutamide in metastatic castration-sensitive prostate cancer in a real-world patient...

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Veröffentlicht in:European urology oncology 2024-11
Hauptverfasser: 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
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Sprache:eng
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Zusammenfassung:ARON-3 is an international, multicenter, retrospective study to collect global experiences in the treatment of patients with advanced prostate cancer. Our results confirm the safety, tolerability, and efficacy of apalutamide in metastatic castration-sensitive prostate cancer in a real-world patient population. 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. PSA90 was defined as a prostate-specific antigen decline of ≥90% from baseline, and PSA0.2 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. PSA90 was experienced by 461 patients (87%) and PSA0.2 by 368 (69%). Median OS was significantly longer for patients with PSA90 or PSA0.2 than for subjects without these responses (p 
ISSN:2588-9311
2588-9311
DOI:10.1016/j.euo.2024.11.005