European Urology Open Science (Dec 2024)

Prostate-specific Antigen at 3 Months as a Predictor of Radiologic Progression-free Survival in Metastatic Hormone-sensitive Prostate Cancer Treated with Apalutamide: Analysis of 633 Patients in a Real-world Database

  • Mario Hassi Roman,
  • Kinga Mate,
  • Pedro De Pablos-Rodriguez,
  • Álvaro Zamora Horcajada,
  • Ana Guijarro Cascales,
  • Ángeles Sanchís Bonet,
  • Antoni Vilaseca,
  • Darío Vázquez-Martul Pazos,
  • Estefanía Linares Espinós,
  • Jesús Muñoz Rodríguez,
  • José Manuel de la Morena Gallego,
  • José Ramón Alemán,
  • Juan Gómez Rivas,
  • Luigi Formisano,
  • Maria J. Juan Fita,
  • Marc Costa Planells,
  • Mario Domínguez Esteban,
  • Meritxell Pérez Márquez,
  • Miguel García Sanz,
  • Nagore García Expósito,
  • Natalia Picola,
  • Pol Servian Vives,
  • Raquel Sopeña Sutil,
  • Miguel A. Climent Durán,
  • Miguel Ramírez Backhaus

Journal volume & issue
Vol. 70
pp. 58 – 63

Abstract

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Background and objective: The depth of the prostate-specific antigen (PSA) decline after androgen receptor pathway inhibitor (ARPI) treatment combined with androgen deprivation therapy for patients with metastatic hormone-sensitive prostate cancer (mHSPC) may affect prognosis. The primary objective in our study was the correlation between the PSA response at 3 mo and radiologic progression-free survival (rPFS) at 24 mo. Three groups were defined according to the PSA decline: complete response (PSA ≤0.02 ng/ml), partial response (PSA >0.02 and ≤0.2 ng/ml), and incomplete response (PSA >0.2 ng/ml). Secondary objectives were correlation between the PSA response at 3 mo and overall survival, and the development of a model predicting complete PSA response. Methods: We conducted a retrospective multicenter study of patients with mHSPC treated with apalutamide from May 2018 to September 2023 registered in the Real-World Evidence APA registry across 20 centers. Key findings and limitations: We included 633 patients with mHSPC. The median age at diagnosis was 68 yr (interquartile range [IQR] 63–75) and median PSA was 16 ng/ml (IQR 7.5–64). Some 63% of the short had low-volume disease, 51% had de novo disease, 48% had recurrent disease. At 3 mo, 27% had a complete response, 42% a partial response, and 31% an incomplete response, with corresponding rRFS rates at 24 mo of 92%, 86%, and 63%. According to the predictive model, a complete PSA response at 3 mo was associated with the use of next-generation imaging and PSA <50 ng/ml at diagnosis. Study limitations include heterogeneity among the groups and variations in data quality and assessment methods. Conclusions and clinical implications: Patients with a complete PSA response after 3 mo of apalutamide treatment face a very low risk of progression within 2 yr. Conversely, nearly 50% of patients with an incomplete PSA response will experience disease progression. Patient summary: For patients with metastatic prostate cancer that is still responsive to hormone therapy, a complete response after treatment with a drug called apalutamide is associated with a very low risk of progression within 2 years. However, nearly half of patients with an incomplete response to apalutamide will experience progression of their cancer.

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