Hassi Roman Mario, Mate Kinga, De Pablos-Rodriguez Pedro, Horcajada Álvaro Zamora, Cascales Ana Guijarro, Bonet Ángeles Sanchís, Vilaseca Antoni, Vázquez-Martul Pazos Darío, Espinós Estefanía Linares, Rodríguez Jesús Muñoz, de la Morena Gallego José Manuel, Alemán José Ramón, Rivas Juan Gómez, Formisano Luigi, Juan Fita Maria J, Planells Marc Costa, Esteban Mario Domínguez, Márquez Meritxell Pérez, Sanz Miguel García, Expósito Nagore García, Picola Natalia, Vives Pol Servian, Sutil Raquel Sopeña, Climent Durán Miguel A, Backhaus Miguel Ramírez
Hospital DIPRECA, Santiago, 7550000, Chile.
Péterfy Sándor Utcai Hospital Clinic and Trauma Centre, Budapest, Hungary.
Eur Urol Open Sci. 2024 Oct 17;70:58-63. doi: 10.1016/j.euros.2024.10.001. eCollection 2024 Dec.
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.
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.
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.
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.
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.
对于转移性激素敏感性前列腺癌(mHSPC)患者,雄激素受体通路抑制剂(ARPI)联合雄激素剥夺治疗后前列腺特异性抗原(PSA)下降的程度可能影响预后。本研究的主要目的是3个月时的PSA反应与24个月时的影像学无进展生存期(rPFS)之间的相关性。根据PSA下降情况定义了三组:完全缓解(PSA≤0.02 ng/ml)、部分缓解(PSA>0.02且≤0.2 ng/ml)和未完全缓解(PSA>0.2 ng/ml)。次要目的是3个月时的PSA反应与总生存期之间的相关性,以及建立预测PSA完全反应的模型。
我们对2018年5月至2023年9月在20个中心登记的Real-World Evidence APA登记处接受阿帕他胺治疗的mHSPC患者进行了一项回顾性多中心研究。
我们纳入了633例mHSPC患者。诊断时的中位年龄为68岁(四分位间距[IQR]63 - 75),中位PSA为16 ng/ml(IQR 7.5 - 64)。约63%的患者疾病体积较小,51%为初发疾病,48%为复发性疾病。3个月时,27%的患者完全缓解,42%部分缓解,31%未完全缓解,24个月时相应的rRFS率分别为92%、86%和63%。根据预测模型,3个月时PSA完全反应与使用新一代影像学检查以及诊断时PSA<50 ng/ml相关。研究局限性包括组间异质性以及数据质量和评估方法的差异。
阿帕他胺治疗3个月后PSA完全反应的患者在2年内进展风险极低。相反,近50%的PSA未完全反应患者会出现疾病进展。
对于仍对激素治疗有反应的转移性前列腺癌患者,使用一种名为阿帕他胺的药物治疗后完全缓解与2年内极低的进展风险相关。然而,近一半对阿帕他胺反应不完全的患者会出现癌症进展。