Al-Samsam Sofya, Bartos Jiri, Samal Vladimir, Dvorak Josef, Kolarova Hana, Richter Igor
Department of Oncology, Regional Hospital Liberec, Czech Republic.
Department of Urology, Regional Hospital Liberec, Czech Republic.
Rep Pract Oncol Radiother. 2024 Mar 18;29(1):1-9. doi: 10.5603/rpor.99028. eCollection 2024.
The aim was to assess therapeutic outcomes and tolerance in patients with metastatic castration resistant prostate cancer (mCRPC) treated with androgen receptor targeted agents (ARTA) treatment at one oncological center in the Czech Republic.
Retrospective analysis of 64 patients with mCRPC treated with abiraterone (50 patients) and enzalutamide (14 patients) in the first line of this disease was conducted. Kaplan-Meier analysis was used to calculate progression free survival (PFS) and overall survival (OS). We performed a multivariate analysis of risk factors for treatment outcomes (PFS, OS) by Cox regression analysis.
The median follow-up was 28.4 months. The median PFS was 15.4 months [95% confidence interval (CI): 12.3-18.5], median OS was 38.2 months (95% CI: 19.9-56.5). Regression analysis demonstrated a favorable prognostic effect on PFS in patients with reduction of PSA ≥ 50 %, in patients with early reduction of prostate-specific antigen (PSA) ≥ 50% within 3 months, in patients younger than 74 years and in overall performance status (PS) 0. Regression analysis demonstrated a favorable prognostic effect on OS in patients with reduction of PSA ≥ 50 %, in patients with early reduction of PSA ≥ 50 % within 3 months and in patients with overall PS 0. Adverse effects grade 3-4 were reported in 17 (27.9%) patients in abirateron arm and in 1 (7.1%) patient in enzalutamide arm.
The analysis of patients with mCRPC treated with ARTA in the first line showed that ARTA represents an effective and safe therapy and contributes to longer survival.
目的是评估在捷克共和国一个肿瘤中心接受雄激素受体靶向药物(ARTA)治疗的转移性去势抵抗性前列腺癌(mCRPC)患者的治疗效果和耐受性。
对64例一线接受阿比特龙(50例)和恩杂鲁胺(14例)治疗的mCRPC患者进行回顾性分析。采用Kaplan-Meier分析计算无进展生存期(PFS)和总生存期(OS)。通过Cox回归分析对治疗结果(PFS、OS)的危险因素进行多因素分析。
中位随访时间为28.4个月。中位PFS为15.4个月[95%置信区间(CI):12.3 - 18.5],中位OS为38.2个月(95%CI:19.9 - 56.5)。回归分析显示,前列腺特异性抗原(PSA)降低≥50%的患者、3个月内PSA早期降低≥50%的患者、年龄小于74岁的患者以及总体表现状态(PS)为0的患者,PFS有良好的预后效果。回归分析显示,PSA降低≥50%的患者、3个月内PSA早期降低≥50%的患者以及总体PS为0的患者,OS有良好的预后效果。阿比特龙组有17例(27.9%)患者报告了3 - 4级不良反应,恩杂鲁胺组有1例(7.1%)患者报告了3 - 4级不良反应。
对一线接受ARTA治疗的mCRPC患者的分析表明,ARTA是一种有效且安全的治疗方法,有助于延长生存期。