Tom Baker Cancer Center, Calgary, Alberta, Canada.
Cancer. 2013 Aug 15;119(16):2999-3006. doi: 10.1002/cncr.28151. Epub 2013 May 21.
This study aimed to apply the International mRCC Database Consortium (IMDC) prognostic model in metastatic non-clear cell renal cell carcinoma (nccRCC). In addition, the survival outcome of metastatic nccRCC patients was characterized.
Data on 2215 patients (1963 with clear-cell RCC [ccRCC] and 252 with nccRCC) treated with first-line VEGF- and mTOR-targeted therapies were collected from the IMDC. Time to treatment failure (TTF) and overall survival (OS) were compared in groups with favorable, intermediate, and poor prognoses according to IMDC prognostic criteria
The median OS of the entire cohort was 20.9 months. nccRCC patients were younger (P < .0001) and more often presented with low hemoglobin (P = .014) and elevated neutrophils (P = .0001), but otherwise had clinicopathological features similar to those of ccRCC patients. OS (12.8 vs 22.3 months; P < .0001) and TTF (4.2 vs 7.8 months; P < .0001) were worse in nccRCC patients compared with ccRCC patients. The hazard ratio for death and TTF when adjusted for the prognostic factors was 1.41 (95% CI, 1.19-1.67; P < .0001) and 1.54 (95% CI, 1.33-1.79; P < .0001), respectively. The IMDC prognostic model reliably discriminated 3 risk groups to predict OS and TTF in nccRCC; the median OS of the favorable, intermediate, and poor prognosis groups was 31.4, 16.1, and 5.1 months, respectively (P < .0001), and the median TTF was 9.6, 4.9, and 2.1 months, respectively (P < .0001).
Although targeted agents have significantly improved the outcome of patients with nccRCC, for the majority survival is still inferior compared with patients with ccRCC. The IMDC prognostic model reliably predicts OS and TTF in nccRCC and ccRCC patients.
本研究旨在将国际转移性肾细胞癌数据库联盟(IMDC)预后模型应用于转移性非透明细胞肾细胞癌(nccRCC)。此外,还对转移性 nccRCC 患者的生存结局进行了特征描述。
从 IMDC 收集了 2215 名接受一线 VEGF 和 mTOR 靶向治疗的患者的数据,其中 1963 名患者患有透明细胞肾细胞癌(ccRCC),252 名患者患有 nccRCC。根据 IMDC 预后标准,比较了预后良好、中等和不良组的治疗失败时间(TTF)和总生存期(OS)。
整个队列的中位 OS 为 20.9 个月。nccRCC 患者更年轻(P < .0001),且更常出现低血红蛋白(P = .014)和高中性粒细胞(P = .0001),但其他临床病理特征与 ccRCC 患者相似。与 ccRCC 患者相比,nccRCC 患者的 OS(12.8 个月 vs 22.3 个月;P < .0001)和 TTF(4.2 个月 vs 7.8 个月;P < .0001)更差。在调整预后因素后,死亡和 TTF 的风险比分别为 1.41(95%CI,1.19-1.67;P < .0001)和 1.54(95%CI,1.33-1.79;P < .0001)。IMDC 预后模型可靠地将 3 个风险组区分开来,以预测 nccRCC 的 OS 和 TTF;预后良好、中等和不良组的中位 OS 分别为 31.4、16.1 和 5.1 个月(P < .0001),中位 TTF 分别为 9.6、4.9 和 2.1 个月(P < .0001)。
尽管靶向药物显著改善了 nccRCC 患者的预后,但对于大多数患者来说,与 ccRCC 患者相比,生存情况仍较差。IMDC 预后模型可靠地预测了 nccRCC 和 ccRCC 患者的 OS 和 TTF。