Department of Comprehensive Cancer Care and Faculty of Medicine, Masaryk Memorial Cancer Institute and Masaryk University, Brno, Czech Republic.
Institute of Biostatistics and Analyses, Faculty of Medcine, Masaryk University, Brno, Czech Republic.
Urol Oncol. 2019 Apr;37(4):294.e1-294.e8. doi: 10.1016/j.urolonc.2018.12.017. Epub 2019 Jan 23.
Nonclear cell renal cell carcinoma (nccRCC) is a heterogeneous group of primary kidney tumors. The aim of the present retrospective study was to analyze outcomes of patients with nccRCC treated with tyrosine-kinase inhibitors (TKIs) based on a national registry.
The registry contained evaluable data of 93 nccRCC patients treated with first-line TKIs, including 87 patients with papillary renal cell carcinoma (RCC) and 6 patients with chromophobe RCC. The control cohort consisted of 1,788 patients with clear-cell RCC treated with first-line TKIs. Multivariable Cox proportional hazard model was used to evaluate the effect of potential prognostic factors on the survival measures.
Median progression-free survival was 11.8 and 6.5 months in the clear cell renal cell carcinoma and nccRCC patients, respectively (P = 0.018), and median overall survival was 33.2 and 22.0 months, respectively (P = 0.007). In the multivariate analysis, independent factors associated with inferior progression-free survival included high tumor grade, worse Memorial Sloan Kettering Cancer Center risk group, absence of nephrectomy, and sunitinib (as opposed to pazopanib) as first-line targeted therapy. Independent predictors of inferior overall survival included nonclear cell histology, tumor grade, worse Memorial Sloan Kettering Cancer Center risk group, absence of nephrectomy, older age, and sunitinib as first-line targeted therapy.
The present retrospective, registry-based study confirms that patients with nccRCC treated with TKIs have worse clinical outcomes compared to clear cell renal cell carcinoma patients with similar baseline characteristics.
非透明细胞肾细胞癌(nccRCC)是一组异质性的原发性肾肿瘤。本回顾性研究的目的是基于国家登记处分析接受酪氨酸激酶抑制剂(TKI)治疗的 nccRCC 患者的结局。
该登记处包含 93 例接受一线 TKI 治疗的 nccRCC 患者的可评估数据,包括 87 例乳头状肾细胞癌(RCC)患者和 6 例嫌色细胞 RCC 患者。对照组由 1788 例接受一线 TKI 治疗的透明细胞 RCC 患者组成。多变量 Cox 比例风险模型用于评估潜在预后因素对生存指标的影响。
透明细胞 RCC 和 nccRCC 患者的中位无进展生存期分别为 11.8 和 6.5 个月(P=0.018),中位总生存期分别为 33.2 和 22.0 个月(P=0.007)。在多变量分析中,与无进展生存期较差相关的独立因素包括高肿瘤分级、较差的 Memorial Sloan Kettering 癌症中心风险组、无肾切除术和舒尼替尼(而非帕唑帕尼)作为一线靶向治疗。总生存期较差的独立预测因素包括非透明细胞组织学、肿瘤分级、较差的 Memorial Sloan Kettering 癌症中心风险组、无肾切除术、年龄较大和舒尼替尼作为一线靶向治疗。
本回顾性基于登记处的研究证实,与具有相似基线特征的透明细胞肾细胞癌患者相比,接受 TKI 治疗的 nccRCC 患者的临床结局更差。