DCE-MRI for Early Prediction of Response in Hepatocellular Carcinoma after TACE and Sorafenib Therapy: A Pilot Study

被引:14
|
作者
Saito, Kazuhiro [1 ]
Ledsam, Joseph [2 ]
Sugimoto, Katsutoshi [1 ]
Sourbron, Steven [2 ]
Araki, Yoichi [1 ]
Tokuuye, Koichi [1 ]
机构
[1] Tokyo Med Univ, Tokyo, Japan
[2] Univ Leeds, Leeds, W Yorkshire, England
基金
英国医学研究理事会;
关键词
DCE-MRI; Tracer kinetic modeling; Sorafenib; TACE; Hepatocellular carcinoma; CONTRAST-ENHANCED MRI; TRANSCATHETER ARTERIAL CHEMOEMBOLIZATION; ENDOTHELIAL GROWTH-FACTOR; GD-EOB-DTPA; LIVER-FUNCTION; BLOOD-FLOW; QUANTIFICATION; CANCER; EXPRESSION; PERFUSION;
D O I
10.5334/jbsr.1278
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Objective: Dynamic contrast-enhanced MRI (DCE-MRI) can measure the changes in tumor blood flow, vascular permeability and interstitial and intravascular volume. The objective was to evaluate the efficacy of DCE-MRI in prediction of Barcelona Clinic Liver Cancer (BCLC) staging B or C hepatocellular carcinoma (HCC) response after treatment with transcatheter arterial chemoembolization (TACE) followed by sorafenib therapy. Methods: Sorafenib was administered four days after TACE of BCLC staging B or C HCC in 11 patients (21 lesions). DCE-MRI was performed with Gd-EOB-DTPA contrast before TACE and three and 10 days after TACE. DCE-MRI acquisitions were taken pre-contrast, hepatic arterial-dominant phase and 60, 120, 180, 240, 330, 420, 510 and 600 seconds post-contrast. Distribution volume of contrast agent (DV) and transfer constant Ktrans were calculated. Patients were grouped by mRECIST after one month or more post-TACE into responders (complete response, partial response) and non-responders (stable disease, progressive disease). Results: DV was reduced in responders at three and 10 days post-TACE (p = 0.008 and p = 0.008 respectively). DV fell in non-responders at three days (p = 0.025) but was not significantly changed from pre-TACE values after sorafenib. Sensitivity and specificity for DV 10 days post-TACE were 88% and 77% respectively. Conclusion: DV may be a useful biomarker for early prediction of therapeutic outcome in intermediate HCC.
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页数:9
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