Guo Ran, Lu Fang, Lin Jiang, Fu Caixia, Liu Mengxiao, Yang Shuohui
Department of Radiology, Shanghai Municipal Hospital of Traditional Chinese Medicine, Shanghai University of Traditional Chinese Medicine, 274 Middle Zhi-jiang Road, Shanghai, 200071, People's Republic of China.
Department of Radiology, Shuguang Hospital Affiliated to Shanghai University of Traditional Chinese Medicine, Shanghai, 201203, People's Republic of China.
Eur Radiol Exp. 2024 Mar 12;8(1):43. doi: 10.1186/s41747-024-00448-y.
Multi-b-value diffusion-weighted imaging (DWI) with different postprocessing models allows for evaluating hepatocellular carcinoma (HCC) proliferation, spatial heterogeneity, and feasibility of treatment strategies. We assessed synergistic effects of bufalin+sorafenib in orthotopic HCC-LM3 xenograft nude mice by using intravoxel incoherent motion (IVIM), diffusion kurtosis imaging (DKI), a stretched exponential model (SEM), and a fractional-order calculus (FROC) model.
Twenty-four orthotopic HCC-LM3 xenograft mice were divided into bufalin+sorafenib, bufalin, sorafenib treatment groups, and a control group. Multi-b-value DWI was performed using a 3-T scanner after 3 weeks' treatment to obtain true diffusion coefficient D, pseudo-diffusion coefficient D, perfusion fraction f, mean diffusivity (MD), mean kurtosis (MK), distributed diffusion coefficient (DDC), heterogeneity index α, diffusion coefficient D, fractional order parameter β, and microstructural quantity μ. Necrotic fraction (NF), standard deviation (SD) of hematoxylin-eosin staining, and microvessel density (MVD) of anti-CD31 staining were evaluated. Correlations of DWI parameters with histopathological results were analyzed, and measurements were compared among four groups.
In the final 22 mice, f positively correlated with MVD (r = 0.679, p = 0.001). Significantly good correlations of MK (r = 0.677), α (r = -0.696), and β (r= -0.639) with SD were observed (all p < 0.010). f, MK, MVD, and SD were much lower, while MD, α, β, and NF were higher in bufalin plus sorafenib group than control group (all p < 0.050).
Evaluated by IVIM, DKI, SEM, and FROC, bufalin+sorafenib was found to inhibit tumor proliferation and angiogenesis and reduce spatial heterogeneity in HCC-LM3 models.
Multi-b-value DWI provides potential metrics for evaluating the efficacy of treatment in HCC.
• Bufalin plus sorafenib combination may increase the effectiveness of HCC therapy. • Multi-b-value DWI depicted HCC proliferation, angiogenesis, and spatial heterogeneity. • Multi-b-value DWI may be a noninvasive method to assess HCC therapeutic efficacy.
采用不同后处理模型的多b值扩散加权成像(DWI)可用于评估肝细胞癌(HCC)的增殖、空间异质性及治疗策略的可行性。我们通过体素内不相干运动(IVIM)、扩散峰度成像(DKI)、拉伸指数模型(SEM)和分数阶微积分(FROC)模型,评估了蟾酥灵+索拉非尼对原位HCC-LM3异种移植裸鼠的协同作用。
将24只原位HCC-LM3异种移植小鼠分为蟾酥灵+索拉非尼组、蟾酥灵组、索拉非尼治疗组和对照组。治疗3周后,使用3-T扫描仪进行多b值DWI,以获得真实扩散系数D、伪扩散系数D*、灌注分数f、平均扩散率(MD)、平均峰度(MK)、分布扩散系数(DDC)、异质性指数α、扩散系数D、分数阶参数β和微观结构量μ。评估坏死分数(NF)、苏木精-伊红染色的标准差(SD)和抗CD31染色的微血管密度(MVD)。分析DWI参数与组织病理学结果的相关性,并比较四组测量值。
在最后的22只小鼠中,f与MVD呈正相关(r = 0.679,p = 0.001)。观察到MK(r = 0.677)、α(r = -0.696)和β(r = -0.639)与SD有显著的良好相关性(所有p < 0.010)。蟾酥灵加索拉非尼组的f、MK、MVD和SD均显著低于对照组,而MD、α、β和NF则高于对照组(所有p < 0.050)。
通过IVIM、DKI、SEM和FROC评估发现,蟾酥灵+索拉非尼可抑制HCC-LM3模型中的肿瘤增殖和血管生成,并降低空间异质性。
多b值DWI为评估HCC治疗效果提供了潜在指标。
• 蟾酥灵加索拉非尼联合使用可能会提高HCC治疗的有效性。 • 多b值DWI描绘了HCC的增殖、血管生成和空间异质性。 • 多b值DWI可能是一种评估HCC治疗效果的非侵入性方法。