Department of Medical Oncology, CHU Bretonneau Centre, Tours University, Tours, France.
Department of Epidemiology, CHU Bretonneau Centre, Tours University, Tours, France.
Clin Genitourin Cancer. 2022 Oct;20(5):495.e1-495.e9. doi: 10.1016/j.clgc.2022.04.004. Epub 2022 Apr 21.
The overall survival (OS) of metastatic castration-resistant prostate cancer (mCRPC) patients has improved since 2011 with the use of novel hormonal agents (NHAs). The incidence of brain metastases (mets) has been reported to increase since 2004 with the use of docetaxel, but not the incidence of visceral mets. Our objective was to study whether the use of NHAs increases the risk of developing visceral or brain mets (VBMs).
mCRPC patients with mets limited to bone (bmCRPC), treated at Tours University Hospital between 2007 and 2015, were included retrospectively. The primary endpoint was to determine whether treatment with NHAs was associated with an increased incidence of VBMs. Secondary endpoints included the search for putative predictive factors to develop VBMs.
On 187 bmCRPC patients included, 65 developed VBMs. VBM incidence increased in bmCRPC patients alive after 2011, compared to patients who died before (39.7 vs. 24.6%, P = .04). Meanwhile, their median OS increased from 16.3 months to 28.5 months (P = .01). The longer was the treatment with NHAs, the lower was the risk of VBMs (HR = 0.96, 95% CI [0.94; 0.99]), whereas age < 70 years (HR = 3.33, 95% CI [1.50; 7.40]) and low PSA level at diagnosis (HR = 1.58, 95% CI [1.16; 2.15]) increased this risk.
Though retrospective, our results showed an increased incidence of VBMs in bmCRPC patients after 2011. However, this was not associated with NHA exposure duration. The role of NHA exposure remains unclear and needs further investigation.
自 2011 年以来,新型激素药物(NHAs)的使用提高了转移性去势抵抗性前列腺癌(mCRPC)患者的总体生存率(OS)。自 2004 年使用多西他赛以来,脑转移(mets)的发生率有所增加,但内脏转移(met)的发生率并未增加。我们的目的是研究 NHAs 的使用是否会增加发生内脏或脑转移(VBMs)的风险。
回顾性纳入 2007 年至 2015 年在图尔大学医院治疗的局限于骨的 mCRPC 患者。主要终点是确定 NHAs 治疗是否与 VBMs 发生率增加相关。次要终点包括寻找可能导致 VBMs 发生的预测因素。
在纳入的 187 例 bmCRPC 患者中,有 65 例发生了 VBMs。与 2011 年前死亡的患者相比,2011 年后存活的 bmCRPC 患者 VBMs 的发生率增加(39.7% vs. 24.6%,P=0.04)。同时,他们的中位 OS 从 16.3 个月延长至 28.5 个月(P=0.01)。NHAs 治疗时间越长,VBMs 的风险越低(HR=0.96,95%CI [0.94;0.99]),而年龄<70 岁(HR=3.33,95%CI [1.50;7.40])和诊断时 PSA 水平较低(HR=1.58,95%CI [1.16;2.15])则增加了这种风险。
尽管是回顾性的,但我们的结果显示,2011 年后 bmCRPC 患者 VBMs 的发生率增加。然而,这与 NHA 暴露时间无关。NHA 暴露的作用仍不清楚,需要进一步研究。