Addition of liver stiffness enhances the predictive accuracy of the PAGE‐B model for hepatitis B‐related hepatocellular carcinoma. Issue 8 (19th January 2021)

• Record Type: Journal Article
• Authors: Chon, Hye Yeon; Lee, Han Ah; Suh, Sang Jun; Lee, Jung Il; Kim, Byung Seok; Kim, In Hee; Lee, Chang Hyeong; Jang, Byoung Kuk; Lee, Hyun Woong; Hwang, Jae Seok; Lee, Chang Hun; Lee, Jin‐Woo; Yu, Jung Hwan; Seo, Yeon Seok; Yim, Hyung Joon; Kim, Seung Up
• Is Part Of: Alimentary pharmacology & therapeutics. Volume 53:Issue 8(2021)
• Page Start: 919
• Page End: 927
• Publication Date: 2021-01-19
• Subjects: Digestive organs -- Diseases -- Treatment -- Periodicals; Digestive organs -- Effect of drugs on -- Periodicals; Gastrointestinal system -- Diseases -- Treatment -- Periodicals; Gastrointestinal system -- Effect of drugs on -- Periodicals; 615.73
• DOI: 10.1111/apt.16267
• Languages: English
• ISSNs: 0269-2813

Abstract

Summary: Background: The modified PAGE‐B (mPAGE‐B) and PAGE‐B models reliably predict the risk of developing chronic hepatitis B (CHB)‐related hepatocellular carcinoma (HCC). Aim(s): To investigate whether the addition of liver stiffness (LS) value, assessed using transient elastography, enhanced the predictive accuracies of these models Methods: Patients with CHB who started anti‐viral therapy (AVT) between 2007 and 2017 were enrolled. The training (Yonsei University Hospital) and validation (seven Korean referral institutes) cohorts contained 1211 and 973 patients, respectively. Results: Based on multivariate analysis, older age (hazard ratio [HR] = 1.051, 95% confidence interval [CI] = 1.031‐1.071), male sex (HR = 2.265, 95% CI = 1.463‐3.506), lower platelet count (HR = 0.993, 95% CI = 0.989‐0.997) and greater LS values (HR = 1.015, 95% CI = 1.002‐1.028) were independently associated with an increased risk of HCC development (all P < 0.05). Thus, we developed a modified PAGE LS ‐B model (maximum score 34) that included age, male sex, platelet count and LS value. The integrated area under the curve of the modified PAGE LS model was greater than those of the PAGE‐B and mPAGE‐B models (0.760 vs 0.714 and 0.716, respectively) in the derivation dataset. The cumulative HCC incidence was significantly higher in the high‐risk (modified PAGE‐B LS score ≥ 24) group than in the intermediate‐risk (modified PAGE LS ‐B score 12‐24) or low‐risk (modified PAGE LS ‐B score < 12) group (all P < 0.001). Similar results were observed in the validation cohort. Conclusions: The predictive accuracies of the PAGE‐B and mPAGE‐B models were validated in Korean patients with CHB receiving AVT. However, the modified PAGE LS ‐B model featuring the addition of LS value showed higher predictability than the PAGE‐B and mPAGE‐B models.