Artificial intelligence predicts direct-acting antivirals failure among hepatitis C virus patients: A nationwide hepatitis C virus registry program

Author:

Lu Ming-Ying,Huang Chung-Feng,Hung Chao-Hung,Tai Chi‐Ming,Mo Lein-Ray,Kuo Hsing-Tao,Tseng Kuo-Chih,Lo Ching-Chu,Bair Ming-Jong,Wang Szu-Jen,Huang Jee-Fu,Yeh Ming-Lun,Chen Chun-Ting,Tsai Ming-Chang,Huang Chien-Wei,Lee Pei-Lun,Yang Tzeng-Hue,Huang Yi-Hsiang,Chong Lee-Won,Chen Chien-Lin,Yang Chi-Chieh,Yang Sheng‐Shun,Cheng Pin-Nan,Hsieh Tsai-Yuan,Hu Jui-Ting,Wu Wen-Chih,Cheng Chien-Yu,Chen Guei-Ying,Zhou Guo-Xiong,Tsai Wei-Lun,Kao Chien-Neng,Lin Chih-Lang,Wang Chia-Chi,Lin Ta-Ya,Lin Chih‐Lin,Su Wei-Wen,Lee Tzong-Hsi,Chang Te-Sheng,Liu Chun-Jen,Dai Chia-Yen,Kao Jia-Horng,Lin Han-Chieh,Chuang Wan-Long,Peng Cheng-Yuan,Tsai Chun-Wei-,Chen Chi-YiORCID,Yu Ming-LungORCID,

Abstract

Background/Aims: Despite the high efficacy of direct-acting antivirals (DAAs), approximately 1–3% of hepatitis C virus (HCV) patients fail to achieve a sustained virological response. We conducted a nationwide study to investigate risk factors associated with DAA treatment failure. Machine-learning algorithms have been applied to discriminate subjects who may fail to respond to DAA therapy.Methods: We analyzed the Taiwan HCV Registry Program database to explore predictors of DAA failure in HCV patients. Fifty-five host and virological features were assessed using multivariate logistic regression, decision tree, random forest, eXtreme Gradient Boosting (XGBoost), and artificial neural network. The primary outcome was undetectable HCV RNA at 12 weeks after the end of treatment. Results: The training (n=23,955) and validation (n=10,346) datasets had similar baseline demographics, with an overall DAA failure rate of 1.6% (n=538). Multivariate logistic regression analysis revealed that liver cirrhosis, hepatocellular carcinoma, poor DAA adherence, and higher hemoglobin A1c were significantly associated with virological failure. XGBoost outperformed the other algorithms and logistic regression models, with an area under the receiver operating characteristic curve of 1.000 in the training dataset and 0.803 in the validation dataset. The top five predictors of treatment failure were HCV RNA, body mass index, α-fetoprotein, platelets, and FIB-4 index. The accuracy, sensitivity, specificity, positive predictive value, and negative predictive value of the XGBoost model (cutoff value=0.5) were 99.5%, 69.7%, 99.9%, 97.4%, and 99.5%, respectively, for the entire dataset.Conclusions: Machine learning algorithms effectively provide risk stratification for DAA failure and additional information on the factors associated with DAA failure.

Funder

Center For Intelligent Drug Systems and Smart Bio-devices

Center of Excellence for Metabolic Associated Fatty Liver Disease, National Sun Yat-sen University, Kaohsiung

Ministry of Education

Publisher

The Korean Association for the Study of the Liver

Subject

Molecular Biology,Hepatology

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