Department of Urology, Keio University School of Medicine, Shinanomachi 35, Shinjuku-ku, Tokyo, 1608582, Japan.
Department of Uro-Oncology, Saitama Medical University International Medical Center, Saitama, Japan.
Int J Clin Oncol. 2019 Sep;24(9):1069-1074. doi: 10.1007/s10147-019-01459-1. Epub 2019 May 7.
The later-line treatment of metastatic renal cell carcinoma (mRCC) has been drastically changing by the development of immune-oncology drugs and molecular targeted treatment in recent years. Although the International Metastatic Renal Cell Carcinoma Database Consortium (IMDC) model is useful for second-line setting, this model has the problem that over 50% patients are classified as intermediate risk group. The aim of this study is to evaluate whether the serum C-reactive protein (CRP) levels prior to second-line treatment could divide intermediate risk group patients.
We retrospectively reviewed 82 consequent intermediate-risk mRCC patients who received second-line molecular targeted therapy. We classified patients who had serum CRP higher than 0.5 mg/dl in elevated CRP group because the median baseline serum CRP level before second-line treatment was 0.51 mg/dl. We assessed the prognostic impact of serum CRP levels prior to second-line treatment initiation to predict overall survival (OS).
Thirty-three out of 82 (40%) patients demonstrated elevated baseline CRP levels. The median OS of elevated and non-elevated CRP group was 11.5 (95% CI 5.4-17.5) and 29.4 (95% CI 25.5-33.5) months, respectively (p = 0.001). The serum CRP elevation could predict prognosis in intermediate risk patients treated with second-line treatment (HR 2.5, 95% CI 1.4-4.2, p = 0.001).
The serum CRP levels after first-line treatment termination could divide intermediate risk group mRCC patients into two prognostic subgroups in second-line targeted treatment setting.
近年来,免疫肿瘤药物和分子靶向治疗的发展极大地改变了转移性肾细胞癌(mRCC)的后线治疗。虽然国际转移性肾细胞癌数据库联盟(IMDC)模型对二线治疗有用,但该模型存在超过 50%的患者被归类为中危组的问题。本研究旨在评估二线治疗前血清 C 反应蛋白(CRP)水平是否可将中危组患者进行分组。
我们回顾性分析了 82 例连续的中危 mRCC 患者,他们接受了二线分子靶向治疗。我们将二线治疗前血清 CRP 高于 0.5mg/dl 的患者归为 CRP 升高组,因为二线治疗前的中位基线血清 CRP 水平为 0.51mg/dl。我们评估了二线治疗前血清 CRP 水平对预测总生存期(OS)的预后影响。
82 例患者中有 33 例(40%)基线 CRP 升高。CRP 升高和非升高组的中位 OS 分别为 11.5(95%CI 5.4-17.5)和 29.4(95%CI 25.5-33.5)个月(p=0.001)。在二线治疗中,血清 CRP 升高可预测中危患者的预后(HR 2.5,95%CI 1.4-4.2,p=0.001)。
一线治疗结束后血清 CRP 水平可将中危 mRCC 患者在二线靶向治疗中分为两个预后亚组。