Department of Radiology, Barts Health NHS Trust, St Bartholomew's Hospital, King George V Building, West Smithfield, London EC1A 7BE, UK.
1] Department of Clinical Physics, Barts Health NHS Trust, St Bartholomew's Hospital, 4th Floor Dominion House, 60 St Bartholomew's Close, London EC1A 7BE, UK [2] Barts and the London NIHR Cardiovascular Biomedical Research Unit, Centre for Advanced Cardiovascular Imaging, Queen Mary University of London, Bonner Road, London E2 9JX, UK.
Br J Cancer. 2014 Feb 4;110(3):616-24. doi: 10.1038/bjc.2013.790. Epub 2013 Dec 24.
Current imaging criteria for categorising disease response in metastatic renal cell carcinoma (mRCC) correlate poorly with overall survival (OS) in patients on anti-angiogenic therapies. We prospectively assess diffusion-weighted and multiphase contrast-enhanced (MCE) MR imaging (MRI) as markers of outcome.
Treatment-naive mRCC patients on a phase II trial using sunitinib completed an MRI substudy. Whole-tumour apparent diffusion coefficient (ADC) maps and histograms were generated, and mean ADC and AUC(low) (proportion of the tumour with ADC values lying below the 25th percentile of the ADC histogram) recorded. On MCE-MRI, regions of interest were drawn around the most avidly enhancing components to analyse enhancement parameters. Baseline (n=26) and treatment-related changes in surviving patients (n=20) were correlated with OS. Imaged metastases were also analysed.
Forty-seven per cent of the patients showed significant changes in whole-tumour mean ADC following therapy, but there was no correlation with outcome. Patients with a high baseline AUC(low) and greater-than-median AUC(low) increase had reduced OS (HR=3.67 (95% confidence interval (CI)=1.23-10.9), P=0.012 and HR=3.72 (95% CI=0.98-14.21), P=0.038, respectively). There was no correlation between MCE-MRI parameters and OS. Twenty-eight metastases were analysed and showed positive correlation with primary tumour mean ADC for individual patients (r=0.607; P<0.001).
Primary RCC ADC histogram analysis shows dynamic changes with sunitinib. Patients in whom the tumour ADC histogram demonstrated high baseline AUC(low) or a greater-than-median increase in AUC(low) with treatment had reduced OS.
目前,用于分类转移性肾细胞癌(mRCC)疾病反应的成像标准与接受抗血管生成治疗的患者的总生存期(OS)相关性较差。我们前瞻性评估扩散加权和多期对比增强(MCE)磁共振成像(MRI)作为预后标志物。
接受舒尼替尼治疗的 II 期试验的治疗初治 mRCC 患者完成了一项 MRI 子研究。生成了全肿瘤表观扩散系数(ADC)图和直方图,并记录了平均 ADC 和 AUC(低值)(肿瘤中 ADC 值低于 ADC 直方图第 25 百分位数的比例)。在 MCE-MRI 上,在最活跃增强成分周围绘制感兴趣区域以分析增强参数。对存活患者(n=20)的基线(n=26)和治疗相关变化与 OS 相关。还分析了成像转移灶。
47%的患者在治疗后全肿瘤平均 ADC 发生显著变化,但与结局无关。基线 AUC(低值)高和 AUC(低值)增加大于中位数的患者 OS 降低(HR=3.67(95%CI=1.23-10.9),P=0.012 和 HR=3.72(95%CI=0.98-14.21),P=0.038)。MCE-MRI 参数与 OS 之间无相关性。分析了 28 个转移灶,发现与个体患者的原发肿瘤平均 ADC 呈正相关(r=0.607;P<0.001)。
原发性 RCC ADC 直方图分析显示舒尼替尼治疗后有动态变化。肿瘤 ADC 直方图基线 AUC(低值)高或治疗后 AUC(低值)增加大于中位数的患者 OS 降低。