Department of Urology, Akita University Graduate School of Medicine, 1-1-1 Hondo, Akita, 010-8543, Japan.
Division of Pathology, Akita University Hospital, Akita, Japan.
Sci Rep. 2020 Nov 18;10(1):20089. doi: 10.1038/s41598-020-77135-6.
Axitinib, a vascular endothelial growth factor receptor-tyrosine kinase inhibitor, will be used in combination first-line therapies against metastatic renal cell carcinoma (mRCC), but its effects as a first-line monotherapy are unclear. Thus, we aimed to elucidate pretreatment clinical factors that predict the prognosis of patients with mRCC receiving first-line axitinib therapy. We enrolled 63 patients with mRCC treated with axitinib as first-line therapy between Nov. 2003 and Jul. 2018. Progression-free survival (PFS) and overall survival (OS) were assessed using the Wald χ statistic in Cox proportional hazards regression. Median patient age was 67 (range: 25-85) years. Seven (11.1%) patients were classified as being at favorable risk, 33 (52.4%) at intermediate risk, and 23 (36.5%) at poor risk according to the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) risk classification system. Median follow-up duration after axitinib initiation was 14 (range: 1-72) months. Median PFS and OS were 18 months and 65 months, respectively. Cox regression analyses of clinical predictors revealed that high C-reactive protein (CRP) levels were significantly correlated with shorter PFS [hazard ratio (HR), 1.63; 95% confidence interval (CI) 1.7-4.0)], whereas spindle cells and poor IMDC risk scores were related to worse OS (HR, 2.87 and 2.88, respectively; 95% CI 1.4-11.0 and 1.1-8.5, respectively). Thus, patients with mRCC and spindle histology or poor IMDC risk scores had worse OS, and those with high CRP levels had shorter PFS in first-line axitinib treatment. Other therapies might be more suitable for initial management of such patients.
阿昔替尼是一种血管内皮生长因子受体酪氨酸激酶抑制剂,将与转移性肾细胞癌(mRCC)的一线治疗联合使用,但作为一线单药治疗的效果尚不清楚。因此,我们旨在阐明预测接受一线阿昔替尼治疗的 mRCC 患者预后的预处理临床因素。我们招募了 63 名接受阿昔替尼一线治疗的 mRCC 患者,这些患者的治疗时间为 2003 年 11 月至 2018 年 7 月。采用 Wald χ 统计量在 Cox 比例风险回归中评估无进展生存期(PFS)和总生存期(OS)。患者年龄中位数为 67 岁(范围:25-85 岁)。根据国际转移性肾细胞癌数据库联盟(IMDC)风险分类系统,7 例(11.1%)患者为低危,33 例(52.4%)为中危,23 例(36.5%)为高危。阿昔替尼治疗开始后中位随访时间为 14 个月(范围:1-72 个月)。中位 PFS 和 OS 分别为 18 个月和 65 个月。临床预测因素的 Cox 回归分析显示,高 C 反应蛋白(CRP)水平与较短的 PFS 显著相关[风险比(HR),1.63;95%置信区间(CI),1.7-4.0],而梭形细胞和较差的 IMDC 风险评分与较差的 OS 相关(HR,分别为 2.87 和 2.88;95%CI,分别为 1.4-11.0 和 1.1-8.5)。因此,患有 mRCC 和梭形组织学或较差的 IMDC 风险评分的患者 OS 较差,而 CRP 水平较高的患者在一线阿昔替尼治疗中 PFS 较短。其他治疗方法可能更适合此类患者的初始治疗。