Teishima Jun, Kobatake Kohei, Shinmei Shunsuke, Inoue Shogo, Hayashi Tetsutaro, Ohara Shinya, Mita Koji, Hasegawa Yasuhisa, Maruyama Satoshi, Kajiwara Mitsuru, Shigeta Masanobu, Mochizuki Hideki, Moriyama Hiroyuki, Fujiwara Seiji, Matsubara Akio
Department of Urology, Graduate School of Biomedical and Health Science, Hiroshima University, Hiroshima, Japan.
Department of Urology, Graduate School of Biomedical and Health Science, Hiroshima University, Hiroshima, Japan.
Urol Oncol. 2017 Nov;35(11):662.e1-662.e7. doi: 10.1016/j.urolonc.2017.07.008. Epub 2017 Aug 1.
The aim of this study was to investigate the effect of kinetics of C-reactive protein (CRP) in the prediction of overall survival (OS) in patients with metastatic renal cell carcinoma (mRCC) treated with a tyrosine kinase inhibitor.
The CRP in 118 cases of molecular-targeted therapy for mRCC was measured before starting the prescription of the first-line targeted agents and at the first time a CT scan was conducted during treatments. All cases were classified into higher-CRP groups and lower ones according to their data at the time of starting treatments. A higher-CRP group was further classified into 2 subgroups based on the kinetics after first-line targeted therapy: "decreased-CRP subgroup" and "nondecreased CRP subgroup."
The median of the observation period was 23.4 months. The OS in cases with CRP higher than 0.5mg/dl was significantly worse than those in other cases (P<0.0001). Multivariate analysis revealed that the pretreated CRP (hazard ratio = 2.093; 95% CI: 1.176-3.858; P = 0.0179) was an independent predictive factor of OS. In the higher-CRP group, the OS for the decreased-CRP subgroup (1 year, 85.0%) was significantly better than those for the nondecreased CRP subgroup (1 year, 37.2%, P<0.0001). Multivariate analyses in the higher-CRP group revealed that the decrease in the CRP was an independent predictive factor for OS (hazard ratio = 0.176; 95% CI: 0.064-0.488; P = 0.0008).
A decrease in CRP as well as pretreatment CRP can be a predictive factor for OS in patients with mRCC treated with a tyrosine kinase inhibitor. Cases with mRCC could be stratified into 3 groups with different prognoses using the pretreated CRP and its changes.
本研究旨在探讨C反应蛋白(CRP)动力学在预测接受酪氨酸激酶抑制剂治疗的转移性肾细胞癌(mRCC)患者总生存期(OS)中的作用。
对118例接受mRCC分子靶向治疗的患者,在开始一线靶向药物治疗前及治疗期间首次进行CT扫描时测定CRP。根据治疗开始时的数据,将所有病例分为高CRP组和低CRP组。高CRP组根据一线靶向治疗后的动力学进一步分为2个亚组:“CRP降低亚组”和“CRP未降低亚组”。
观察期中位数为23.4个月。CRP高于0.5mg/dl的患者的OS明显差于其他患者(P<0.0001)。多因素分析显示,治疗前CRP(风险比=2.093;95%CI:1.176-3.858;P=0.0179)是OS的独立预测因素。在高CRP组中,CRP降低亚组的OS(1年,85.0%)明显优于CRP未降低亚组(1年,37.2%,P<0.0001)。高CRP组的多因素分析显示,CRP降低是OS的独立预测因素(风险比=0.176;95%CI:0.064-0.488;P=0.0008)。
CRP降低以及治疗前CRP可作为接受酪氨酸激酶抑制剂治疗的mRCC患者OS的预测因素。使用治疗前CRP及其变化,mRCC病例可分为3个预后不同的组。