Department of Urology, Hamamatsu University School of Medicine, 1-20-1 Handayama, Higashi-Ku, Hamamatsu, 431-3192, Japan.
Int J Clin Oncol. 2019 Jul;24(7):842-847. doi: 10.1007/s10147-019-01412-2. Epub 2019 Feb 9.
To compare the prognostic outcomes between first-generation antiandrogen (FGA) and novel androgen-receptor-axis-targeted agent (ARATA) as first-line therapy in patients with non-metastatic castration-resistant prostate cancer (nmCRPC).
This study retrospectively included a total of 103 consecutive nmCRPC patients consisting of 47 (45.6%) and 56 (54.4%) who received FGA (bicalutamide or flutamide) and ARATA (abiraterone acetate or enzalutamide), respectively, as the first-line agent after the failure of primary androgen deprivation therapy (ADT).
There were no significant differences in the major clinicopathological parameters and previous therapeutic histories between the FGA and ARATA groups. During the observation period, 31 (66.0%) and 29 (51.8%) discontinued first-line therapy in the FGA and ARATA groups, respectively, and of these, 27 (87.1%) and 23 (79.3%) in the FGA and ARATA groups, respectively, were subsequently treated with approved agents as second-line therapy. The prostate-specific antigen (PSA) response rate in the FGA group was significantly lower than that in the ARATA group. Although no significant difference in overall survival was noted between the FGA and ARATA groups, there were significant differences in the PSA progression-free survival on first-line therapy and metastasis-free survival between the two groups, favoring the ARATA group compared with FGA group.
Collectively, these findings suggest that among nmCRPC patients who progressed following treatment with the primary ADT, the introduction of ARATA may result in the delay of disease progression compared with FGA.
比较第一代抗雄激素药物(FGA)和新型雄激素受体轴靶向药物(ARATA)作为一线治疗药物在非转移性去势抵抗性前列腺癌(nmCRPC)患者中的预后结局。
本研究回顾性纳入了 103 例连续的 nmCRPC 患者,其中 47 例(45.6%)和 56 例(54.4%)分别接受了 FGA(比卡鲁胺或氟他胺)和 ARATA(醋酸阿比特龙或恩扎卢胺)作为一线治疗药物,这些患者均在原发性去势治疗(ADT)失败后。
FGA 和 ARATA 组之间在主要临床病理参数和既往治疗史方面没有显著差异。在观察期间,FGA 和 ARATA 组分别有 31 例(66.0%)和 29 例(51.8%)停止了一线治疗,其中 FGA 和 ARATA 组分别有 27 例(87.1%)和 23 例(79.3%)随后接受了批准的二线治疗药物。FGA 组的前列腺特异性抗原(PSA)反应率明显低于 ARATA 组。虽然 FGA 和 ARATA 组之间的总生存没有显著差异,但在一线治疗的 PSA 无进展生存和无转移生存方面存在显著差异,ARATA 组优于 FGA 组。
总体而言,这些发现表明,在接受原发性 ADT 治疗后进展的 nmCRPC 患者中,与 FGA 相比,引入 ARATA 可能会延迟疾病进展。