探索P53突变肝细胞癌的磁共振成像和临床特征

IF 4.2 3区 医学 Q2 ONCOLOGY Journal of Hepatocellular Carcinoma Pub Date : 2024-08-29 eCollection Date: 2024-01-01 DOI:10.2147/JHC.S462979
Jingfei Weng, Yuyao Xiao, Jing Liu, Xiaohua Liu, Yuqing He, Fei Wu, Xiaoyan Ni, Chun Yang
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引用次数: 0

摘要

目的:研究P53突变型肝细胞癌(HCC)患者的磁共振成像特征(基于LI-RADS)和临床特征:本研究共纳入344例经组织病理学证实的HCC患者(P53突变组[n = 196],非P53突变组[n = 148])。我们回顾性地评估了术前磁共振成像特征、病灶的临床和病理特征,并根据 LI-RADS 对每个病灶进行了分级。采用Student's t检验、χ2检验和多变量回归分析对MRI结果、临床特征和病理结果进行比较:结果:大多数 HCC 患者被归类为 LR-5。多变量分析发现,Edmondson-Steiner 分级(几率比为 2.280;95% CI:1.268,4.101;P = 0.006)和边缘增强(几率比为 2.517;95% CI:1.095,5.784;P = 0.030)是与 P53 突变的 HCC 相关的独立变量。在最大肿瘤直径(LTD)大于或等于 10 毫米且小于或等于 20 毫米的 HCC 病变组中,增强囊是 P53 突变 HCC 的独立预测因子(几率比,6.200;95% CI:1.116,34.449;P = 0.037)。在 HCC 病变(20 mm ˂ LTD ≤ 50 mm)中,发现电晕增强(几率比,2.102;95% CI:1.022,4.322;P = 0.043)和结节内结节结构(几率比,2.157;95% CI:1.033,4.504;P = 0.041)是 P53 突变的独立危险因素。在HCC病变(50 mm ˂ LTD ≤ 100 mm)中,直径(几率比,1.035;95% CI:1.001,1.069;p = 0.044)和AFP≥400(ng/mL)(几率比,3.336;95% CI:1.052,10.577;p = 0.041)是与P53突变HCC相关的独立变量:分化不良和边缘增强是预测P53突变HCC的潜在生物标志物,而不同直径的HCC在预测P53突变方面具有不同的风险因素。
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Exploring the MRI and Clinical Features of P53-Mutated Hepatocellular Carcinoma.

Purpose: To study the MRI features (based on LI-RADS) and clinical characteristics of P53-mutated hepatocellular carcinoma (HCC) patients.

Patients and methods: This study enrolled 344 patients with histopathologically confirmed HCC (P53-mutated group [n = 196], non-P53-mutated group [n = 148]). We retrospectively evaluated the preoperative MRI features, clinical and pathologic features of the lesions and assigned each lesion according to the LI-RADS. MRI findings, clinical features, and pathologic findings were compared using the Student's t test, χ2 test, and multivariable regression analysis.

Results: Most HCC patients were categorized as LR-5. On multivariate analysis, the Edmondson-Steiner grade (odds ratio, 2.280; 95% CI: 1.268, 4.101; p = 0.006) and rim enhancement (odds ratio, 2.517; 95% CI: 1.095, 5.784; p = 0.030) were found to be independent variables associated with P53-mutated HCC. In the group of HCC lesions with the largest tumor diameter (LTD) greater than or equal to 10mm and less than or equal to 20mm, enhancing capsule was an independent predictor of P53-mutated HCC (odds ratio, 6.200; 95% CI: 1.116, 34.449; p = 0.037). Among the HCC lesions (20 mm ˂ LTD ≤ 50 mm), corona enhancement (odds ratio, 2.102; 95% CI: 1.022, 4.322; p = 0.043) and nodule-in-nodule architecture (odds ratio, 2.157; 95% CI: 1.033, 4.504; p = 0.041) were found to be independent risk factors for P53 mutation. Among the HCC lesions (50 mm ˂ LTD ≤ 100 mm), diameter (odds ratio, 1.035; 95% CI: 1.001, 1.069; p = 0.044) and AFP ≥ 400 (ng/mL) (odds ratio, 3.336; 95% CI: 1.052, 10.577; p = 0.041) were found to be independent variables associated with P53-mutated HCC.

Conclusion: Poor differentiation and rim enhancement are potential predictive biomarkers for P53-mutated HCC, while HCCs of different diameters have different risk factors for predicting P53 mutations.

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