Clinical Nomogram Model for Pre-Operative Prediction of Microvascular Invasion of Hepatocellular Carcinoma before Hepatectomy

Author:

Chen Jen-Lung1ORCID,Chen Yaw-Sen1,Hsieh Kun-Chou1,Lee Hui-Ming1,Chen Chung-Yen1,Chen Jian-Han1,Hung Chao-Ming2,Hsu Chao-Tien3,Huang Ya-Ling4,Ker Chen-Guo1ORCID

Affiliation:

1. Department of General Surgery, E-Da Hospital, I-Shou University, Kaohsiung 824, Taiwan

2. Department of General Surgery, E-Da Cancer Hospital, I-Shou University, Kaohsiung 824, Taiwan

3. Department of Pathology, E-Da Hospital, I-Shou University, Kaohsiung 824, Taiwan

4. Cancer Registration Center, E-Da Cancer Hospital, I-Shou University, Kaohsiung 824, Taiwan

Abstract

Background and Objectives: Microvascular invasion (MVI) significantly impacts recurrence and survival rates after liver resection in hepatocellular carcinoma (HCC). Pre-operative prediction of MVI is crucial in determining the treatment strategy. This study aims to develop a nomogram model to predict the probability of MVI based on clinical features in HCC patients. Materials and Methods: A total of 489 patients with a pathological diagnosis of HCC were enrolled from our hospital. Those registered from 2012–2015 formed the derivation cohort, and those from 2016–2019 formed the validation cohort for pre-operative prediction of MVI. A nomogram model for prediction was created using a regression model, with risk factors derived from clinical and tumor-related features before surgery. Results: Using the nomogram model to predict the odds ratio of MVI before hepatectomy, the AFP, platelet count, GOT/GPT ratio, albumin–alkaline phosphatase ratio, ALBI score, and GNRI were identified as significant variables for predicting MVI. The Youden index scores for each risk variable were 0.287, 0.276, 0.196, 0.185, 0.115, and 0.112, respectively, for the AFP, platelet count, GOT/GPT ratio, AAR, ALBI, and GNRI. The maximum value of the total nomogram scores was 220. An increase in the number of nomogram points indicated a higher probability of MVI occurrence. The accuracy rates ranged from 55.9% to 64.4%, and precision rates ranged from 54.3% to 68.2%. Overall survival rates were 97.6%, 83.4%, and 73.9% for MVI(−) and 80.0%, 71.8%, and 41.2% for MVI(+) (p < 0.001). The prognostic effects of MVI(+) on tumor-free survival and overall survival were poor in both the derivation and validation cohorts. Conclusions: Our nomogram model, which integrates clinical factors, showed reliable calibration for predicting MVI and provides a useful tool enabling surgeons to estimate the probability of MVI before resection. Consequently, surgical strategies and post-operative care programs can be adapted to improve the prognosis of HCC patients where possible.

Funder

E-Da Hospital

Publisher

MDPI AG

Reference57 articles.

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