Kwak Cheol, Park Yong Hyun, Jeong Chang Wook, Jeong Hyeon, Lee Sang Eun, Moon Kyung Chul, Ku Ja Hyeon
Department of Urology, Seoul National University Hospital, Seoul, Korea.
J Surg Oncol. 2007 Mar 15;95(4):317-23. doi: 10.1002/jso.20669.
The objective of the current study was to determine the significance of sarcomatoid differentiation as a prognostic factor for immunotherapy in metastatic renal cell carcinoma (RCC).
Patients with metastatic RCC were included in this study and were categorized according to sarcomatoid differentiation.
Patients with sarcomatoid differentiation had more aggressive tumor characteristics than those without sarcomatoid differentiation. After immunotherapy, the median progression-free survival was 9.0 months (95% confidence interval [CI] 1.4-52.7) for patient without sarcomatoid differentiation and 3.2 months (95% CI 0.4-42.9) for patients with sarcomatoid differentiation, respectively (P=0.0001). The median overall survival was 22.2 months (95% CI 3.2-75.4) and 10.0 months (95% CI 0.7-60.1) in both groups. When comparing patients with sarcomatoid differentiation, there was no significant difference of overall survival in the immunotherapy group and the no immunotherapy group. Multivariate Cox proportional hazards model analysis showed that T stage (Hazard ratio [HR] 1.71; 95% CI 1.07-2.74; P=0.024), sarcomatoid differentiation (HR 2.18; 95% CI 1.30-3.66; P = 0.003), and the number of metastasis sites (HR 1.81; 95% CI 1.14-2.88; P=0.012) were independent predictors of progression-free survival. Sarcomatoid differentiation and the number of metastasis sites were independent prognostic predictors of overall survival. The estimated relative risks of sarcomatoid differentiation and the number of metastasis sites were 2.83 (95% CI 1.49-5.40; P=0.002) and 2.31 (95% CI 1.29-4.16; P=0.005), respectively.
Our findings suggest that sarcomatoid differentiation is an important prognostic factor for immunotherapy in metastatic RCC.
本研究的目的是确定肉瘤样分化作为转移性肾细胞癌(RCC)免疫治疗预后因素的意义。
本研究纳入了转移性RCC患者,并根据肉瘤样分化进行分类。
肉瘤样分化的患者比无肉瘤样分化的患者具有更具侵袭性的肿瘤特征。免疫治疗后,无肉瘤样分化的患者中位无进展生存期为9.0个月(95%置信区间[CI]1.4 - 52.7),有肉瘤样分化的患者为3.2个月(95%CI 0.4 - 42.9),差异有统计学意义(P = 0.0001)。两组的中位总生存期分别为22.2个月(95%CI 3.2 - 75.4)和10.0个月(95%CI 0.7 - 60.1)。比较有肉瘤样分化的患者时,免疫治疗组和非免疫治疗组的总生存期无显著差异。多因素Cox比例风险模型分析显示,T分期(风险比[HR]1.71;95%CI 1.07 - 2.74;P = 0.024)、肉瘤样分化(HR 2.18;95%CI 1.30 - 3.66;P = 0.003)和转移部位数量(HR 1.81;95%CI 1.14 - 2.88;P = 0.012)是无进展生存期的独立预测因素。肉瘤样分化和转移部位数量是总生存期的独立预后预测因素。肉瘤样分化和转移部位数量的估计相对风险分别为2.83(95%CI 1.49 - 5.40;P = 0.002)和2.31(95%CI 1.29 - 4.16;P = 0.005)。
我们的研究结果表明,肉瘤样分化是转移性RCC免疫治疗的重要预后因素。