Hypothetical treatment of patients with non-alcoholic steatohepatitis: Potential impact on important clinical outcomes

被引:2
|
作者
Younossi, Zobair M. [1 ,2 ]
Tampi, Radhika P. [1 ]
Nader, Fatema [3 ]
Younossi, Issah M. [3 ]
Cable, Rebecca [2 ]
Srishord, Manirath [2 ]
Racila, Andrei [1 ,3 ]
机构
[1] Inova Hlth Syst, Betty & Guy Beatty Ctr Integrated Res, 3300 Gallows Rd, Falls Church, VA 22042 USA
[2] Inova Fairfax Hosp, Ctr Liver Dis, Dept Med, Falls Church, VA USA
[3] Ctr Outcomes Res Liver Dis, Washington, DC USA
关键词
economic analysis; Markov modelling; NASH treatment; FATTY LIVER-DISEASE; HEPATOCELLULAR-CARCINOMA; METABOLIC SYNDROME; CURRENT KNOWLEDGE; FIBROSIS STAGE; TRANSPLANTATION; PREVALENCE; MORTALITY; CIRRHOSIS; SURVIVAL;
D O I
10.1111/liv.14292
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Background & Aims Currently, standard of care (SOC) treatment for NASH is limited to lifestyle modifications. Drug regimens are being evaluated currently. We assessed the impact of a short-term hypothetical treatment on clinical outcomes of NASH. Methods Markov models estimated differences in outcomes between SOC and 2 hypothetical NASH treatments (A and B). We modelled 10 000 50-year-old biopsy-proven NASH patients over lifetime horizon. Health states included NASH with fibrosis (F1-F3), cirrhosis, hepatocellular carcinoma, liver transplant and mortality. Fibrosis Regression Factor (FRF) variable modelled the probability of 1-3 stage fibrosis improvement with treatment. Annual probability of treatment (ATP) ranged from 10%-70%. Treatment success was defined as regression to fibrosis, whereas failure was defined as progression to stages beyond cirrhosis. In treatment-A, successful treatment was followed by a maintenance regimen which stopped disease progression. After a successful treatment-B, patients remained at risk of disease progression. Differences in outcomes were calculated between both treatments and SOC models. We conducted a probabilistic sensitivity analysis. Results At 10% to 70% ATP, treatment-A averts 353 to 782 liver transplants and 1277 to 2381 liver-related deaths relative to SOC. Treatment-B averts 129 to 437 liver transplants and 386 to 1043 liver-related deaths. Sensitivity analysis shows our model is robust in estimating liver-related mortality and LTs averted, but is sensitive when estimating QALYs gained. Conclusions With a small annual probability of treatment and FRF = 1, a 2-year treatment followed by maintenance of histologic improvement for patients would be highly beneficial relative to short-term treatment alone.
引用
收藏
页码:308 / 318
页数:11
相关论文
共 50 条
  • [31] Non-alcoholic steatohepatitis
    Dancygier, H
    DEUTSCHE MEDIZINISCHE WOCHENSCHRIFT, 2001, 126 (33) : 930 - 930
  • [32] Non-Alcoholic Steatohepatitis
    不详
    GENETIC ENGINEERING & BIOTECHNOLOGY NEWS, 2008, 28 (20): : 61 - 61
  • [33] Non-alcoholic steatohepatitis
    Romero-Gomez, Manuel
    MEDICINA CLINICA, 2022, 159 (08): : 388 - 395
  • [34] Non-alcoholic steatohepatitis
    Caballería, J
    Rodés, J
    MEDICINA CLINICA, 2003, 120 (17): : 670 - 675
  • [35] Non-alcoholic steatohepatitis
    Saibara, T
    Onishi, S
    Ogawa, T
    Yoshida, S
    Enzan, H
    LANCET, 1999, 354 (9186): : 1299 - 1300
  • [36] Non-alcoholic steatohepatitis
    Petit, P
    Zarski, JP
    GASTROENTEROLOGIE CLINIQUE ET BIOLOGIQUE, 2000, 24 (02): : 157 - 159
  • [37] Non-alcoholic steatohepatitis
    Brierley, Rob
    LANCET GASTROENTEROLOGY & HEPATOLOGY, 2018, 3 (06): : 379 - 379
  • [38] Non-alcoholic fatty liver disease and non-alcoholic steatohepatitis in patients with HIV
    Verna, Elizabeth C.
    LANCET GASTROENTEROLOGY & HEPATOLOGY, 2017, 2 (03): : 211 - 223
  • [39] Clinical trial: pilot study of metformin for the treatment of non-alcoholic steatohepatitis
    Loomba, R.
    Lutchman, G.
    Kleiner, D. E.
    Ricks, M.
    Feld, J. J.
    Borg, B. B.
    Modi, A.
    Nagabhyru, P.
    Sumner, A. E.
    Liang, T. J.
    Hoofnagle, J. H.
    ALIMENTARY PHARMACOLOGY & THERAPEUTICS, 2009, 29 (02) : 172 - 182
  • [40] Pathophysiology of Non-Alcoholic Steatohepatitis and Basis for Treatment
    Pinzani, Massimo
    DIGESTIVE DISEASES, 2011, 29 (02) : 243 - 248