Optimal Timing of Hepatitis C Treatment for Patients on the Liver Transplant Waiting List

被引:74
作者
Chhatwal, Jagpreet [1 ]
Samur, Sumeyye
Kues, Brian
Ayer, Turgay
Roberts, Mark S.
Kanwal, Fasiha
Hur, Chin
Donnell, Drew Michael S.
Chung, Raymond T. [2 ,3 ]
机构
[1] Massachusetts Gen Hosp, Inst Technol Assessment, 101 Merrimac St,Floor 10, Boston, MA 02114 USA
[2] Massachusetts Gen Hosp, Ctr Liver, Boston, MA 02114 USA
[3] Massachusetts Gen Hosp, Gastrointestinal Div, Boston, MA 02114 USA
基金
美国国家卫生研究院; 美国国家科学基金会;
关键词
SOFOSBUVIR PLUS RIBAVIRIN; QUALITY-OF-LIFE; VIRUS-INFECTION; UNITED-STATES; DECOMPENSATED CIRRHOSIS; COST-EFFECTIVENESS; GENOTYPE; GRAFT CIRRHOSIS; HCV INFECTION; DISEASE;
D O I
10.1002/hep.28926
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The availability of oral direct-acting antivirals has altered the hepatitis C virus (HCV) treatment paradigm for both preliver transplant (LT) and post-LT patients. There is a perceived trade-off between pre-LT versus post-LT treatment of HCV-treatment may improve liver function but potentially decrease the likelihood of a necessary LT. Our objective was to identify LT-eligible patients with decompensated cirrhosis who would benefit (and not benefit) from pre-LT treatment based on their Model for End-Stage Liver Disease (MELD) scores. We simulated a virtual trial comparing long-term outcomes of pre-LT versus post-LT HCV treatment with oral direct-acting antivirals for patients with MELD scores between 10 and 40. We developed a Markov-based microsimulation model, which simulated the life course of patients on the transplant waiting list and after LT. Simulation of LT integrated data from recent trials of oral direct-acting antivirals (SOLAR 1 and 2), the United Network for Organ Sharing (UNOS), and other studies. The outcomes of the model included life expectancy, 1-year and 5-year patient survival, and mortality. Model-predicted patient survival was validated with UNOS data. We found that, at the national level, treating HCV before LT increased life expectancy if MELD was <= 27 but could decrease life expectancy at higher MELD scores. Depending on the UNOS region, the threshold MELD score to treat HCV pre-LT varied between 23 and 27 and was lower for UNOS regions 3, 10, and 11 and higher for regions 1, 2, 4, 5, 8, and 9. Sensitivity analysis showed that the thresholds were stable. Conclusion: Our findings suggest that the optimal MELD threshold below which decompensated cirrhosis patients should receive HCV treatment while awaiting LT is between 23 and 27, depending on the UNOS region.
引用
收藏
页码:777 / 788
页数:12
相关论文
共 40 条
[1]   The optimal timing of living-donor liver transplantation [J].
Alagoz, O ;
Maillart, LM ;
Schaefer, AJ ;
Roberts, MS .
MANAGEMENT SCIENCE, 2004, 50 (10) :1420-1430
[2]   Natural history of clinically compensated hepatitis C virus-related graft cirrhosis after liver transplantation [J].
Berenguer, M ;
Prieto, M ;
Rayón, JM ;
Mora, J ;
Pastor, M ;
Ortiz, V ;
Carrasco, D ;
San Juan, F ;
Burgueño, MDJ ;
Mir, J ;
Berenguer, J .
HEPATOLOGY, 2000, 32 (04) :852-858
[3]   Contribution of donor age to the recent decrease in patient survival among HCV-infected liver transplant recipients [J].
Berenguer, M ;
Prieto, M ;
San Juan, F ;
Rayón, JM ;
Martinez, F ;
Carrasco, D ;
Moya, A ;
Orbis, F ;
Mir, J ;
Berenguer, J .
HEPATOLOGY, 2002, 36 (01) :202-210
[4]   Treat chronic hepatitis C virus infection in decompensated cirrhosis - pre- or post-liver transplantation? the ironic conundrum in the era of effective and well-tolerated therapy [J].
Bunchorntavakul, C. ;
Reddy, K. Rajender .
JOURNAL OF VIRAL HEPATITIS, 2016, 23 (06) :408-418
[5]   Management of Hepatitis C Before and After Liver Transplantation in the Era of Rapidly Evolving Therapeutic Advances [J].
Bunchorntavakul, Chalermrat ;
Reddy, K. Rajender .
JOURNAL OF CLINICAL AND TRANSLATIONAL HEPATOLOGY, 2014, 2 (02) :124-133
[6]   Model for end-stage liver disease limbo, model for end-stage liver disease purgatory, and the dilemma of treating hepatitis C in patients awaiting liver transplantation [J].
Carrion, Andres F. ;
Khaderi, Saira A. ;
Sussman, Norman L. .
LIVER TRANSPLANTATION, 2016, 22 (03) :279-280
[7]   Ledipasvir and Sofosbuvir Plus Ribavirin for Treatment of HCV Infection in Patients With Advanced Liver Disease [J].
Charlton, Michael ;
Everson, Gregory T. ;
Flamm, Steven L. ;
Kumar, Princy ;
Landis, Charles ;
Brown, Robert S., Jr. ;
Fried, Michael W. ;
Terrault, Norah A. ;
O'Leary, Jacqueline G. ;
Vargas, Hugo E. ;
Kuo, Alexander ;
Schiff, Eugene ;
Sulkowski, Mark S. ;
Gilroy, Richard ;
Watt, Kymberly D. ;
Brown, Kimberly ;
Kwo, Paul ;
Pungpapong, Surakit ;
Korenblat, Kevin M. ;
Muir, Andrew J. ;
Teperman, Lewis ;
Fontana, Robert J. ;
Denning, Jill ;
Arterburn, Sarah ;
Dvory-Sobol, Hadas ;
Brandt-Sarif, Theo ;
Pang, Phillip S. ;
McHutchison, John G. ;
Reddy, K. Rajender ;
Afdhal, Nezam .
GASTROENTEROLOGY, 2015, 149 (03) :649-659
[8]  
Cheung M, 2016, LANCET, V387, P26
[9]   Hepatitis C Disease Burden in the United States in the era of oral direct-acting antivirals [J].
Chhatwal, Jagpreet ;
Wang, Xiaojie ;
Ayer, Turgay ;
Kabiri, Mina ;
Chung, Raymond T. ;
Hur, Chin ;
Donohue, Julie M. ;
Roberts, Mark S. ;
Kanwal, Fasiha .
HEPATOLOGY, 2016, 64 (05) :1442-1450
[10]   Cost-Effectiveness and Budget Impact of Hepatitis C Virus Treatment With Sofosbuvir and Ledipasvir in the United States [J].
Chhatwal, Jagpreet ;
Kanwal, Fasiha ;
Roberts, Mark S. ;
Dunn, Michael A. .
ANNALS OF INTERNAL MEDICINE, 2015, 162 (06) :397-U114