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新型雄激素受体信号抑制剂治疗转移性激素敏感前列腺癌患者的临床结局和风险分层。

Clinical Outcomes and Risk Stratification in Patients With Metastatic Hormone-Sensitive Prostate Cancer Treated With New-Generation Androgen Receptor Signaling Inhibitors.

机构信息

Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.

Division of Urology, Kobe University Graduate School of Medicine, Kobe, Japan.

出版信息

Clin Genitourin Cancer. 2024 Oct;22(5):102140. doi: 10.1016/j.clgc.2024.102140. Epub 2024 Jun 14.

DOI:10.1016/j.clgc.2024.102140
PMID:39018723
Abstract

BACKGROUND

Optimal drug selection for metastatic hormone-sensitive prostate cancer (mHSPC) remains unclear. We therefore assessed the clinical outcomes of mHSPC treated with new-generation androgen receptor pathway inhibitors (ARSIs) and identified risk factors associated with the prognosis of mHSPC.

METHODS

We retrospectively reviewed 324 patients with mHSPC who were treated with ARSIs, including abiraterone acetate, enzalutamide, and apalutamide, between January 2018 and December 2022. In addition to assessing the prostate-specific antigen (PSA) response and overall survival (OS) during ARSI treatment, we investigated several potential risk factors for a poor OS in patients with mHSPC.

RESULTS

Patients with a ≥ 90% PSA reduction (hazard ratio [HR]: 0.24, 95% confidence interval [CI], 0.10-0.58; P = .002) and those whose PSA declined to ≤ 0.2 ng/mL (HR: 0.22, 95% CI, 0.08-0.63; P = .005) showed significantly better OS than other patients. Gleason grade group 5 (GG5), presence of liver metastasis, and an LDH ≥ 250 U/L were identified as prognostic factors significantly associated with a poor OS, with HRs of 2.31 (95% CI, 1.02-5.20; P = .044), 7.87 (95% CI, 2.61-23.8; P < .001) and 3.21 (95% CI, 1.43-7.23; P = .005).

CONCLUSION

We identified GG5, the presence of liver metastasis, and elevated LDH at the diagnosis as significant factors predicting the OS of mHSPC, but the choice of ARSIs did not affect the prognosis. The potential prognostic impact of these markers requires further investigation.

摘要

背景

转移性去势敏感型前列腺癌(mHSPC)的最佳药物选择仍不明确。因此,我们评估了使用新一代雄激素受体通路抑制剂(ARSIs)治疗 mHSPC 的临床结局,并确定了与 mHSPC 预后相关的危险因素。

方法

我们回顾性分析了 2018 年 1 月至 2022 年 12 月期间接受 ARSIs(醋酸阿比特龙、恩扎卢胺和阿帕他胺)治疗的 324 例 mHSPC 患者。除了评估 ARSI 治疗期间前列腺特异性抗原(PSA)反应和总生存期(OS)外,我们还研究了 mHSPC 患者 OS 不良的几个潜在危险因素。

结果

PSA 降低≥90%的患者(风险比[HR]:0.24,95%置信区间[CI]:0.10-0.58;P=0.002)和 PSA 降低至≤0.2ng/mL 的患者(HR:0.22,95%CI:0.08-0.63;P=0.005)的 OS 明显更好。Gleason 分级组 5(GG5)、肝转移存在和乳酸脱氢酶(LDH)≥250U/L 被确定为与 OS 不良显著相关的预后因素,HR 分别为 2.31(95%CI:1.02-5.20;P=0.044)、7.87(95%CI:2.61-23.8;P<0.001)和 3.21(95%CI:1.43-7.23;P=0.005)。

结论

我们确定了 GG5、肝转移存在和诊断时 LDH 升高是预测 mHSPC OS 的重要因素,但 ARSIs 的选择并不影响预后。这些标志物的潜在预后影响需要进一步研究。

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