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Diffusion-weighted MR imaging of advanced hepatocellular carcinoma treated with the oral multikinase inhibitor Sorafenib

机译:用口服多立糖酶抑制剂索拉非尼治疗晚期肝细胞癌的扩散加权MR成像

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To evaluate diffusion-weighted imaging (DWI) in the response monitoring of hepatocellular carcinoma (HCC) treated with the oral multikinase inhibitor Sorafenib. Materials and Methods: 10 patients with histologically proven advanced HCC were examined on a 1.5 T whole-body-unit before and during Sorafenib therapy. Navigator-respiratory triggered echoplanar imaging (EPI) DWI with b-values of 50/400/800 s/mm was performed in addition to the standard liver protocol. Size, location and ADC were recorded for designated target lesions before and during Sorafenib therapy. ADC changes were analyzed with regard to potential diagnostic information for treatment monitoring Results: Mean time-to-progression was 6.6 months. All lesions showed an initial ADC decrease in the first MR scan 4 weeks after onset of Sorafenib. Areas of ADC reduction could be attributed to focal hyperintensities in the non-enhanced Tl images, suggesting intralesional hemorrhage. In the second MR scan 10 weeks after treatment onset, the majority of lesions showed re-increasing ADC values. In the long-term follow-up, constant ADC decline was observed in the majority of lesions. Conclusion: HCC lesions exhibit characteristic but unusual ADC changes during Sorafenib therapy. The ADC changes reflect pathophysiologic mechanisms in the tumor (most probably hemorrhagic necrosis) induced by this novel targeted agent early after therapy onset. In the long-term follow-up, changes in DWI may indicate tumor progression.
机译:评价用口服多立糖酶抑制剂索拉非尼治疗的肝细胞癌(HCC)的响应监测中的扩散加权成像(DWI)。材料和方法:10例组织学验证先进的HCC患者在索拉芬皮治疗前后的1.5吨全体单元上检查。除标准肝协议外,导航仪 - 呼吸触发的回波血管成像(EPI)DWI为50/400 / 800S / mm的B值。在Sorafenib疗法之前和期间,记录了尺寸,位置和ADC的指定目标病变。关于治疗监测结果的潜在诊断信息分析ADC变化:平均进展为6.6个月。所有病变均显示初始ADC在索拉非尼开始后4周的第一次Mr扫描中减少。 ADC减少区域可归因于非增强TL图像中的焦势,表明腔内出血。在治疗发作后10周的第二个MR扫描中,大多数病变显示了再增加的ADC值。在长期随访中,大多数病变中观察到持续的ADC下降。结论:HCC病变表现出Sorafenib治疗期间的特征但不寻常的ADC变化。 ADC改变反映了在治疗发作后早期肿瘤(大概有可能出血性坏死)的病理生理机制。在长期随访中,DWI的变化可能表明肿瘤进展。

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