Prognostic Factors for Transplant-Free Survival and Validation of Prognostic Models in Chinese Patients with Primary Biliary Cholangitis Receiving Ursodeoxycholic Acid

被引:42
作者
Cheung, Ka-Shing [1 ]
Seto, Wai-Kay [1 ,2 ]
Fung, James [1 ,2 ]
Lai, Ching-Lung [1 ,2 ]
Yuen, Man-Fung [1 ,2 ]
机构
[1] Univ Hong Kong, Queen Mary Hosp, Dept Med, Pokfulam Rd, Hong Kong, Hong Kong, Peoples R China
[2] Univ Hong Kong, State Key Lab Liver Res, Hong Kong, Hong Kong, Peoples R China
关键词
BIOCHEMICAL RESPONSE; RISK STRATIFICATION; CONTROLLED-TRIAL; CIRRHOSIS; PROGRESSION; BILIRUBIN; VALUES;
D O I
10.1038/ctg.2017.23
中图分类号
R57 [消化系及腹部疾病];
学科分类号
100201 [内科学];
摘要
OBJECTIVES: We aimed to validate the prognostic models for primary biliary cholangitis (PBC) in Chinese patients receiving ursodeoxycholic acid (UCDA), and to compare their performances in predicting the long-term survival. METHODS: Chinese patients with PBC from a tertiary center were identified via electronic search of hospital medical registry. Risk factors associated with adverse events (liver transplantation or death from liver-related causes including hepatocellular carcinoma (HCC) and liver decompensation) were determined. Transplant-free survival was defined as survival free of liver-related death or transplantation. RESULTS: Of the 144 patients, 41 (28.5%) had baseline cirrhosis. The median age at diagnosis was 57.8 years. During a median follow-up of 7.0 years, 40 patients died (21 liver-related; 19 non-liver-related), 12 developed HCC, and 10 underwent transplantations. The 5-, 10-, and 15-year transplant-free survival probabilities were 91.0%, 78.1%, and 58.9%, respectively. Independent risk factors for adverse events were increasing age (hazard ratio (HR) 1.05), cirrhosis (HR 8.53), and suboptimal treatment response (HR 3.06). Aspartate aminotransferase/platelet ratio index at 1 year (APRI-r1) in combination with treatment response optimized the risk stratification. The performances of the GLOBE, UK-PBC scores, Rotterdam criteria, and APRI-r1 were comparable in predicting adverse events. The area under receiver operating curves within 5, 10, and 15 years were as follows-GLOBE score: 0.83, 0.85, and 0.85, respectively; UK-PBC score: 0.89, 0.83, and 0.79, respectively; Rotterdam criteria: 0.82, 0.76, and 0.80, respectively; APRI-r1: 0.80, 0.83, and 0.77, respectively. CONCLUSIONS: The UK-PBC, GLOBE scores, Rotterdam criteria, and APRI-r1 had good and comparable prognostic prediction values for Chinese PBC patients receiving UCDA.
引用
收藏
页数:10
相关论文
共 31 条
[1]
EASL Clinical Practice Guidelines: Management of cholestatic liver diseases [J].
Beuers, Ulrich ;
Boberg, Kirsten M. ;
Chapman, Roger W. ;
Chazouilleres, Olivier ;
Invernizzi, Pietro ;
Jones, David E. J. ;
Lammert, Frank ;
Pares, Albert ;
Trauner, Michael .
JOURNAL OF HEPATOLOGY, 2009, 51 (02) :237-267
[2]
Clinical significance of serum bilirubin levels under ursodeoxycholic acid therapy in patients with primary biliary cirrhosis [J].
Bonnand, AM ;
Heathcote, EJ ;
Lindor, KD ;
Poupon, RE .
HEPATOLOGY, 1999, 29 (01) :39-43
[3]
Management of Hepatocellular Carcinoma: An Update [J].
Bruix, Jordi ;
Sherman, Morris .
HEPATOLOGY, 2011, 53 (03) :1020-1022
[4]
The UK-PBC Risk Scores: Derivation and Validation of a Scoring System for Long-Term Prediction of End-Stage Liver Disease in Primary Biliary Cholangitis [J].
Carbone, Marco ;
Sharp, Stephen J. ;
Flack, Steve ;
Paximadas, Dimitrios ;
Spiess, Kelly ;
Adgey, Carolyn ;
Griffiths, Laura ;
Lim, Reyna ;
Trembling, Paul ;
Williamson, Kate ;
Wareham, Nick J. ;
Aldersley, Mark ;
Bathgate, Andrew ;
Burroughs, Andrew K. ;
Heneghan, Michael A. ;
Neuberger, James M. ;
Thorburn, Douglas ;
Hirschfield, Gideon M. ;
Cordell, Heather J. ;
Alexander, Graeme J. ;
Jones, David E. J. ;
Sandford, Richard N. ;
Mells, George F. .
HEPATOLOGY, 2016, 63 (03) :930-950
[5]
Sex and Age Are Determinants of the Clinical Phenotype of Primary Biliary Cirrhosis and Response to Ursodeoxycholic Acid [J].
Carbone, Marco ;
Mells, George F. ;
Pells, Greta ;
Dawwas, Muhammad F. ;
Newton, Julia L. ;
Heneghan, Michael A. ;
Neuberger, James M. ;
Day, Darren B. ;
Ducker, Samantha J. ;
Sandford, Richard N. ;
Alexander, Graeme J. ;
Jones, David E. J. .
GASTROENTEROLOGY, 2013, 144 (03) :560-+
[6]
Primary biliary cirrhosis [J].
Carey, Elizabeth J. ;
Ali, Ahmad H. ;
Lindor, Keith D. .
LANCET, 2015, 386 (10003) :1565-1575
[7]
Primary biliary cirrhosis autoimmune hepatitis overlap syndrome:: Clinical features and response to therapy [J].
Chazouillères, O ;
Wendum, D ;
Serfaty, L ;
Montembault, S ;
Rosmorduc, O ;
Poupon, R .
HEPATOLOGY, 1998, 28 (02) :296-301
[8]
Biochemical response to ursodeoxycholic acid and long-term prognosis in primary biliary cirrhosis [J].
Corpechot, Christophe ;
Abenavoli, Ludovico ;
Rabahi, Nabila ;
Chretien, Yves ;
Andreani, Tony ;
Johanet, Catherine ;
Chazouilleres, Olivier ;
Poupon, Raoul .
HEPATOLOGY, 2008, 48 (03) :871-877
[9]
Noninvasive elastography-based assessment of liver fibrosis progression and prognosis in primary biliary cirrhosis [J].
Corpechot, Christophe ;
Carrat, Fabrice ;
Poujol-Robert, Armelle ;
Gaouar, Farid ;
Wendum, Dominique ;
Chazouilleres, Olivier ;
Poupon, Raoul .
HEPATOLOGY, 2012, 56 (01) :198-208
[10]
Early primary biliary cirrhosis: Biochemical response to treatment and prediction of long-term outcome [J].
Corpechot, Christophe ;
Chazouilleres, Olivier ;
Poupon, Raoul .
JOURNAL OF HEPATOLOGY, 2011, 55 (06) :1361-1367