Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Japan
Department of Urology, Hamamatsu University School of Medicine, Hamamatsu, Japan.
Anticancer Res. 2020 Feb;40(2):1101-1106. doi: 10.21873/anticanres.14049.
BACKGROUND/AIM: Despite recent introduction of several novel agents, limited data exist regarding parameters that help predict the progression of non-metastatic castration-resistant prostate cancer (nmCRPC). The objective of this study was to identify prognostic predictors in nmCRPC patients.
This study included 127 consecutive Japanese nmCRPC patients treated in routine clinical practice. Prognostic outcomes in these patients were analyzed to evaluate the impact of several parameters on prostate-specific antigen progression-free survival (PSA PFS) and metastasis-free survival (MFS).
When the 127 patients were diagnosed with nmCRPC, the PSA and PSA doubling time (PSADT) were 13.5 ng/ml and 17.9 months, respectively. Of these, 77 (60.6%) and 50 (39.4%) were treated with first-generation anti-androgen (FGA) and novel androgen-receptor-axis-targeted agent (ARATA), respectively, as first-line therapy for nmCRPC. The median PSA PFS and MFS after the diagnosis of nmCRPC in these patients were 29.5 months and not reached, respectively. Multivariate analyses identified the following independent prognostic factors: PSA at nmCRPC, PSADT and first-line therapy for nmCRPC for PSA PFS, and PSA at nmCRPC and PSADT for MFS.
nmCRPC patients with higher PSA and/or shorter PSADT should be treated with ARATA rather than FGA.
背景/目的:尽管最近引入了几种新型药物,但关于有助于预测非转移性去势抵抗性前列腺癌(nmCRPC)进展的参数的数据有限。本研究的目的是确定 nmCRPC 患者的预后预测指标。
本研究纳入了 127 例连续的日本 nmCRPC 患者,他们在常规临床实践中接受治疗。分析这些患者的预后结果,以评估几种参数对前列腺特异性抗原无进展生存期(PSA PFS)和无转移生存期(MFS)的影响。
当这 127 例患者被诊断为 nmCRPC 时,PSA 和 PSA 倍增时间(PSADT)分别为 13.5ng/ml 和 17.9 个月。其中,77 例(60.6%)和 50 例(39.4%)分别接受第一代抗雄激素(FGA)和新型雄激素受体轴靶向药物(ARATA)作为 nmCRPC 的一线治疗。这些患者在诊断为 nmCRPC 后的 PSA PFS 和 MFS 的中位值分别为 29.5 个月和未达到。多变量分析确定了以下独立的预后因素:nmCRPC 时的 PSA、PSADT 和 nmCRPC 的一线治疗对 PSA PFS,以及 nmCRPC 时的 PSA 和 PSADT 对 MFS。
nmCRPC 患者的 PSA 较高和/或 PSADT 较短,应接受 ARATA 治疗而不是 FGA 治疗。