Abstract

BackgroundPredicting the long-term prognosis of individuals who experienced sorafenib treatment following partial hepatectomy due to hepatitis B virus (HBV) related hepatocellular carcinoma (HCC) is difficult. This work aims to create an effective prognostic nomogram for HBV related HCC patients who are receiving sorafenib treatment as adjuvant therapy after surgery.MethodsA total of 233 HBV-related HCC patients treated with or without sorafenib following partial hepatectomy at the Eastern Hepatobiliary Surgery Hospital from 2008 to 2013 were matched with propensity score matching analysis. The optimal cut-off point of the overall survival (OS) factor level was determined by x-tile. The selection of indicators was based on clinical findings. The Cox regression model with an interaction term was employed for evaluating the predictive value. Using a multivariate Cox proportional hazards model, a nomogram was subsequently formulated to analyze 111 patients treated with sorafenib. The nomogram’s discriminative ability and predictive accuracy were determined using the concordance index (C-index), calibration, and ROC curve.ResultsThe matched sorafenib cohort of 111 patients and control cohort of 118 patients were analyzed. Subgroup analysis revealed that low GPC3, pERK, pAKT, serum AFP levels, without MVI, under 50 years old, male, TNM stage I/II and BCLC stage 0/A were significantly associated with a better OS in patients subjected to sorafenib treatment compared to those without sorafenib treatment after surgery. Multivariate analysis of the sorafenib cohort revealed GPC3, pERK, pAKT, serum AST, and BCLC stage as independent factors for OS, and all were included in the nomogram. The survival probability based on the calibration curve showed that the prediction of the nomogram was in good agreement with the actual observation. The C-index of the nomogram for predicting survival was 0.73(95% CI, 0.67–0.78). The area under the ROC curve (AUC) for the nomogram to predict the survival for 1, 3, and 5-year was 0.726, 0.816, and 0.823, respectively.ConclusionThis proposed nomogram shows the potential to make a precise prediction regarding the prognosis of HBV-related HCC patients and may help to stratify patients for personalized therapy following partial hepatectomy.

Highlights

  • Predicting the long-term prognosis of individuals who experienced sorafenib treatment following partial hepatectomy due to hepatitis B virus (HBV) related hepatocellular carcinoma (HCC) is difficult

  • To investigate different aspects related to the advantages of sorafenib in HCC patients, 233 patients who went through surgery between April 2008 and February 2013 at Eastern Hepatobiliary Surgery Hospital (EHBH) were enrolled in this study

  • Sample size calculation showed that 216 patients needed to be randomized, and the power value was 0.8012 (Table.S1). 118 of 120 HCC patients without sorafenib therapy were matched to 111of 113 HCC patients who have received sorafenib therapy by propensity scores

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Summary

Introduction

Predicting the long-term prognosis of individuals who experienced sorafenib treatment following partial hepatectomy due to hepatitis B virus (HBV) related hepatocellular carcinoma (HCC) is difficult. A clinical trial showed reduced mortality and prolonged overall survival for Abbreviations: ALT, Alanine aminotransferase; AST, Aspartate transaminase; AUC, The area under the ROC curve; C-index, Concordance index; FDA, Food and Drug Administration; GPC3, Glypican-3; HBcAb, Hepatitis B core antibody; HBsAg, Hepatitis B surface antigen; HBV, Hepatitis B virus; HCC, Hepatocellular carcinoma; HCV, Hepatitis C virus; HE, Hematoxylin-eosin; HGF, Hepatocyte growth factor; IFN, Interferon; IHC, Immunohistochemistry; MAPK/ERK, Mitogen-activated protein kinase/extracellular signal-regulated kinase; MRI, Magnetic resonance imaging; OS, Overall survival; pAKT, Phosphorylated AKT; pERK, Phosphorylated ERK; ROC, Receiver operating characteristic; TBIL, Total bilirubin; TNM, Tumor-node-metastasis classification system; TTR, Time to recurrence; VEGFR, Vascular endothelial growth factor receptors; WHO, World Health Organization

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