Department of Medical Imaging, Sunnybrook Health Sciences Center, University of Toronto, Rm AG-46, 2075 Bayview Ave, Toronto, Onatrio, M4N 3M5, Canada.
Department of Radiology, North Bristol NHS Trust, Southmead Hospital, Bristol, UK.
Cancer Imaging. 2017 Jan 23;17(1):4. doi: 10.1186/s40644-017-0106-8.
To assess CT texture based quantitative imaging biomarkers in the prediction of progression free survival (PFS) and overall survival (OS) in patients with clear cell renal cell carcinoma undergoing treatment with Sunitinib.
In this retrospective study, measurable lesions of 40 patients were selected based on RECIST criteria on standard contrast enhanced CT before and 2 months after treatment with Sunitinib. CT Texture analysis was performed using TexRAD research software (TexRAD Ltd, Cambridge, UK). Using a Cox regression model, correlation of texture parameters with measured time to progression and overall survival were assessed. Evaluation of combined International Metastatic Renal-Cell Carcinoma Database Consortium Model (IMDC) score with texture parameters was also performed.
Size normalized standard deviation (nSD) alone at baseline and follow-up after treatment was a predictor of OS (Hazard ratio (HR) = 0.01 and 0.02; 95% confidence intervals (CI): 0.00 - 0.29 and 0.00 - 0.39; p = 0.01 and 0.01). Entropy following treatment and entropy change before and after treatment were both significant predictors of OS (HR = 2.68 and 87.77; 95% CI = 1.14 - 6.29 and 1.26 - 6115.69; p = 0.02 and p = 0.04). nSD was also a predictor of PFS at baseline and follow-up (HR = 0.01 and 0.01: 95% CI: 0.00 - 0.31 and 0.001 - 0.22; p = 0.01 and p = 0.003). When nSD at baseline or at follow-up was combined with IMDC, it improved the association with OS and PFS compared to IMDC alone.
Size normalized standard deviation from CT at baseline and follow-up scans is correlated with OS and PFS in clear cell renal cell carcinoma treated with Sunitinib.
评估 CT 纹理定量成像生物标志物在接受舒尼替尼治疗的透明细胞肾细胞癌患者中无进展生存期(PFS)和总生存期(OS)的预测价值。
在这项回顾性研究中,根据 RECIST 标准,在接受舒尼替尼治疗前后的标准增强 CT 上选择了 40 名患者的可测量病变。使用 TexRAD 研究软件(TexRAD Ltd,英国剑桥)进行 CT 纹理分析。使用 Cox 回归模型,评估纹理参数与测量的进展时间和总生存时间的相关性。还评估了联合国际转移性肾细胞癌数据库联盟模型(IMDC)评分与纹理参数的相关性。
仅基线和治疗后随访时的大小归一化标准差(nSD)是 OS 的预测因子(危险比(HR)分别为 0.01 和 0.02;95%置信区间(CI)分别为 0.00-0.29 和 0.00-0.39;p 值分别为 0.01 和 0.01)。治疗后熵和治疗前后熵变化均是 OS 的显著预测因子(HR 分别为 2.68 和 87.77;95%CI 分别为 1.14-6.29 和 1.26-6115.69;p 值分别为 0.02 和 0.04)。nSD 也是基线和随访时 PFS 的预测因子(HR 分别为 0.01 和 0.01;95%CI 分别为 0.00-0.31 和 0.001-0.22;p 值分别为 0.01 和 0.003)。当基线或随访时的 nSD 与 IMDC 相结合时,与 OS 和 PFS 的相关性优于单独的 IMDC。
基线和随访时 CT 大小归一化标准差与接受舒尼替尼治疗的透明细胞肾细胞癌患者的 OS 和 PFS 相关。