Ueda Kosuke, Suekane Shigetaka, Nishihara Kiyoaki, Suekane Hiroki, Ogasawara Naoyuki, Kurose Hirofumi, Chikui Katsuaki, Ejima Kazuhisa, Suyama Shunsuke, Nakiri Makoto, Matsuo Mitsunori, Igawa Tsukasa
Department of Urology, Kurume University School of Medicine, Kurume, Fukuoka 830-0011, Japan.
Mol Clin Oncol. 2017 Aug;7(2):205-210. doi: 10.3892/mco.2017.1294. Epub 2017 Jun 15.
The aim of the present study was to investigate the prognostic factors for patients with primary unresectable renal cell carcinoma (RCC) with synchronous distant metastasis receiving molecularly targeted therapies. A total of 26 patients with primary unresectable RCC with synchronous distant metastasis underwent molecularly targeted therapies at the Kurume University Hospital (Kurume, Japan) between March 2008 and March 2016. Early primary renal tumor response was evaluated at 8-12 weeks after the introduction of molecularly targeted therapy and a 10% decrease in the diameter of primary renal tumor was used as the cut-off value. The median overall survival from the initiation of first-line molecularly targeted therapy was 18.3 months. Univariate analyses for various factors identified early primary renal tumor response (P=0.0004) and best response to first-line treatment (P=0.0002) as prognostic variables. Multivariate analyses also identified early primary renal tumor response (P=0.0099) and best response to first-line treatment (P=0.0054) as independent prognostic factors. A comparison of clinical characteristics between the group with ≥10% shrinkage and the group with disease progression or <10% shrinkage revealed that the number of metastatic sites and pretreatment monocyte-to-lymphocyte ratio tended to be predictive factors for primary renal tumor response. These results suggest that early primary renal tumor shrinkage is highly variable for patients with primary unresectable RCC with synchronous distant metastasis receiving molecularly targeted therapies.
本研究的目的是调查接受分子靶向治疗的原发性不可切除肾细胞癌(RCC)伴同步远处转移患者的预后因素。2008年3月至2016年3月期间,共有26例原发性不可切除RCC伴同步远处转移的患者在日本久留米大学医院接受了分子靶向治疗。在引入分子靶向治疗后8 - 12周评估早期原发性肾肿瘤反应,以原发性肾肿瘤直径减少10%作为临界值。从一线分子靶向治疗开始的中位总生存期为18.3个月。对各种因素的单因素分析确定早期原发性肾肿瘤反应(P = 0.0004)和对一线治疗的最佳反应(P = 0.0002)为预后变量。多因素分析也确定早期原发性肾肿瘤反应(P = 0.0099)和对一线治疗的最佳反应(P = 0.0054)为独立预后因素。对收缩率≥10%的组与疾病进展或收缩率<10%的组之间的临床特征进行比较,结果显示转移部位数量和治疗前单核细胞与淋巴细胞比率倾向于成为原发性肾肿瘤反应的预测因素。这些结果表明,对于接受分子靶向治疗的原发性不可切除RCC伴同步远处转移的患者,早期原发性肾肿瘤缩小情况差异很大。