New Thresholds for AFP and Des-γ-Carboxy Prothrombin in Chronic Liver Disease Depending on the Use of Nucleoside Analogs and an Integrated Nomogram

Ting Sun,1 Ruicen Li,2 Yiwen Qiu,1 Shu Shen,1 Wentao Wang1 1Department of Liver Surgery & Liver Transplantation Center, West China Hospital of Sichuan University, Chengdu, People’s Republic of China; 2Health Management Center, West China Hospital of Sichuan University, Chengdu, People’s Republic...

Full description

Bibliographic Details
Main Authors: Sun T, Li R, Qiu Y, Shen S, Wang W
Format: Article
Language:English
Published: Dove Medical Press 2021-09-01
Series:International Journal of General Medicine
Subjects:
Online Access:https://www.dovepress.com/new-thresholds-for-afp-and-des--carboxy-prothrombin-in-chronic-liver-d-peer-reviewed-fulltext-article-IJGM
Description
Summary:Ting Sun,1 Ruicen Li,2 Yiwen Qiu,1 Shu Shen,1 Wentao Wang1 1Department of Liver Surgery & Liver Transplantation Center, West China Hospital of Sichuan University, Chengdu, People’s Republic of China; 2Health Management Center, West China Hospital of Sichuan University, Chengdu, People’s Republic of ChinaCorrespondence: Wentao WangDepartment of Liver Surgery & Liver Transplantation Center, West China Hospital of Sichuan University, 37 Guoxue Road, Chengdu, 610041, People’s Republic of ChinaTel +86 18980601895Email wwtdoctor02@163.comBackground: The thresholds of alpha-fetoprotein (AFP) and des-gamma-carboxy prothrombin (PIVKA-II) when detecting hepatocellular carcinoma (HCC) in chronic hepatitis B (CHB) patients with antiviral nucleoside analog (NA) remain controversial. A relevant integrated nomogram needs to be developed.Methods: We enrolled a consecutive series of 5666 cases diagnosed with CHB either with or without antiviral agents and randomly allocated them to the training set (n=3966, 70.00%) and the validation set (n=1700, 30.00%).Results: In the training set, the levels of AFP and PIVKA-II of NA-treated patients were significantly lower than those of untreated patients. The most appropriate cut-off values of AFP and PIVKA-II were 151.40 ng/mL (a sensitivity of 39.77% and a specificity of 92.17%) and 35.50 mAU/mL (a sensitivity of 84.85% and a specificity of 69.43%) for NA-treated patients. As for BCLC-0/A HCC, the most appropriate cut-off values of AFP and PIVKA-II were 151.40 ng/mL and 32.50 mAU/mL for NA-treated patients, respectively. A logistic regression model composed of AFP, PIVKA-II and other clinical parameters to predict the risk of HBV-related HCC for NA-treated patients was established and verified to have an AUROC of 0.868 (95% CI, 0.827– 0.909) for all-stage HCC and an AUROC of 0.856 (95% CI, 0.809– 0.903) for BCLC-0/A HCC.Conclusion: The new detection thresholds of AFP and PIVKA-II might lead to the ability to perform early detection for hepatoma in NA-treated patients and the innovative risk prediction model is a valuable tool for identifying high-risk CHB patients.Keywords: hepatitis B virus, hepatocellular carcinoma, alpha-fetoprotein, des-gamma-carboxy prothrombin, antiviral agents, nomogram
ISSN:1178-7074