首页> 外文会议>World congress on medical physics and biomedical engineering;International congress of the IUPESM >Diffusion-weighted MR imaging of advanced hepatocellular carcinoma treated with the oral multikinase inhibitor Sorafenib
【24h】

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

机译:口服多激酶抑制剂索拉非尼治疗晚期肝癌的扩散加权MR成像

获取原文

摘要

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 monitoringResults: 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:为了评估扩散加权成像(DWI)在口服多激酶抑制剂索拉非尼治疗的肝细胞癌(HCC)的反应监测中。 材料和方法:在索拉非尼治疗之前和治疗期间,对经组织学证实为晚期肝癌的10例患者进行1.5 T全身检查。除标准肝协议外,还执行了b值为50/400/800 s / mm的导航仪-呼吸触发的超声回波平面成像(EPI)DWI。在索拉非尼治疗之前和期间记录指定目标病变的大小,位置和ADC。针对治疗监测的潜在诊断信息对ADC的变化进行了分析 结果:平均进展时间为6.6个月。索拉非尼起病后4周,在所有MR扫描中,所有病变均显示ADC初始降低。 ADC减少的区域可能归因于未增强的T1图像中的局灶性高信号,提示病灶内出血。在治疗开始后10周的第二次MR扫描中,大多数病变显示ADC值再次增加。在长期随访中,大多数病变均观察到ADC持续下降。 结论:索拉非尼治疗期间HCC病变表现出特征性但异常的ADC变化。 ADC的变化反映了这种新的靶向药物在治疗开始后诱发的肿瘤(最可能是出血性坏死)的病理生理机制。在长期的随访中,DWI的改变可能表明肿瘤的进展。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号