Nomogram development and validation to predict hepatocellular carcinoma tumor behavior by preoperative gadoxetic acid-enhanced MRI

• Published in: European radiology Vol. 31; no. 11; pp. 8615 - 8627
• Main Authors: Tang, Mimi, Zhou, Qian, Huang, Mengqi, Sun, Kaiyu, Wu, Tingfan, Li, Xin, Liao, Bing, Chen, Lili, Liao, Junbin, Peng, Sui, Chen, Shuling, Feng, Shi-Ting
• Format: Journal Article
• Language: English
• Published: Berlin/Heidelberg Springer Berlin Heidelberg 01.11.2021; Springer Nature B.V
• Subjects: Acids; Alanine; Alanine transaminase; Diagnostic Radiology; Differentiation; Diffusion coefficient; Hepatobiliary-Pancreas; Hepatocellular carcinoma; Image enhancement; Imaging; Immunology; Internal Medicine; Interventional Radiology; Liver cancer; Magnetic resonance imaging; Medicine; Medicine & Public Health; Microvasculature; Neuroradiology; Nomograms; Patients; Pretreatment; Prognosis; Radiology; Relaxation time; Training; Tumor microenvironment; Tumors; Ultrasound; α-Fetoprotein; Carcinoma, hepatocellular; Biology; Magnetic resonance imaging; Nomograms; Gadolinium ethoxybenzyl DTPA
• ISSN: 0938-7994; 1432-1084
• DOI: 10.1007/s00330-021-07941-7

Objectives Pretreatment evaluation of tumor biology and microenvironment is important to predict prognosis and plan treatment. We aimed to develop nomograms based on gadoxetic acid-enhanced MRI to predict microvascular invasion (MVI), tumor differentiation, and immunoscore. Methods This retrospective study included 273 patients with HCC who underwent preoperative gadoxetic acid-enhanced MRI. Patients were assigned to two groups: training ( N = 191) and validation ( N = 82). Univariable and multivariable logistic regression analyses were performed to investigate clinical variables and MRI features’ associations with MVI, tumor differentiation, and immunoscore. Nomograms were developed based on features associated with these three histopathological features in the training cohort, then validated, and evaluated. Results Predictors of MVI included tumor size, rim enhancement, capsule, percent decrease in T1 images (T1 D %), standard deviation of apparent diffusion coefficient, and alanine aminotransferase levels, while capsule, peritumoral enhancement, mean relaxation time on the hepatobiliary phase (T1 E ), and alpha-fetoprotein levels predicted tumor differentiation. Predictors of immunoscore included the radiologic score constructed by tumor number, intratumoral vessel, margin, capsule, rim enhancement, T1 D %, relaxation time on plain scan (T1 P ), and alpha-fetoprotein and alanine aminotransferase levels. Three nomograms achieved good concordance indexes in predicting MVI (0.754, 0.746), tumor differentiation (0.758, 0.699), and immunoscore (0.737, 0.726) in the training and validation cohorts, respectively. Conclusion MRI-based nomograms effectively predict tumor behaviors in HCC and may assist clinicians in prognosis prediction and pretreatment decisions. Key Points • This study developed and validated three nomograms based on gadoxetic acid-enhanced MRI to predict MVI, tumor differentiation, and immunoscore in patients with HCC. • The pretreatment prediction of tumor microenvironment may be useful to guide accurate prognosis and planning of surgical and immunological therapies for individual patients with HCC.