A proposal from the liver forum for the management of comorbidities in non-alcoholic steatohepatitis therapeutic trials

被引:9
|
作者
Pais, Raluca [1 ,2 ]
Cariou, Bertrand [3 ]
Noureddin, Mazen [4 ]
Francque, Sven [5 ,6 ]
Schattenberg, Joern M. [7 ]
Abdelmalek, Manal F. [8 ]
Lalazar, Gadi [9 ]
Varma, Sharat [10 ]
Dietrich, Julie [11 ]
Miller, Veronica [12 ]
Sanyal, Arun [13 ]
Ratziu, Vlad [1 ,14 ]
机构
[1] Sorbonne Univ, Hop Pitie Salpetriere, Assistance Publ Hop Paris, Inst Cardiometab & Nutr, Paris, France
[2] Ctr Rech St Antoine, INSERM UMRS 938, Paris, France
[3] Nantes Univ, CNRS, CHU Nantes, INSERM,Inst Thorax, F-44000 Nantes, France
[4] Houston Res Inst, Houston, TX USA
[5] Antwerp Univ Hosp, Dept Gastroenterol Hepatol, Drie Eikenstr 655, B-2650 Edegem, Belgium
[6] Univ Antwerp, Fac Med & Hlth Sci, InflaMed Ctr Excellence,Belgium European Referenc, Lab Expt Med & Paediat Translat Sci Inflammat & I, Univ Pl 1, B-2610 Antwerp, Belgium
[7] Johannes Gutenberg Univ Mainz, Univ Med Ctr, Dept Med 1, Metab Liver Res Program, Mainz, Germany
[8] Duke Univ, Div Gastroenterol & Hepatol, Durham, NC USA
[9] Shaare Zedek Med Ctr, Digest Dis Inst, Liver Unit, Jerusalem, Israel
[10] Novo Nordisk AS, Vandtarnsvej 108-110, DK-2860 Soborg, Denmark
[11] GENFIT, Parc Eurasante 885,Ave Eugene Avinee, F-59120 Loos, France
[12] Univ Calif Berkeley, Forum Collaborat Res, Sch Publ Hlth, Berkeley, CA USA
[13] Virginia Commonwealth Univ, Sch Med, Richmond, VA USA
[14] INSERM UMRS 1138 CRC, Paris, France
关键词
NAFLD; NASH; fibrosis; diabetes; obesity; metabolic syndrome; arterial hypertension; dyslipidemia; randomized placebo-controlled trials; run-in period; RUN-IN PERIODS; LOW-DENSITY LIPOPROTEIN; FATTY LIVER; CLINICAL-TRIALS; FOLLOW-UP; CARDIOVASCULAR-DISEASE; WEIGHT-LOSS; HEPATOCELLULAR CANCER; INDEPENDENT PREDICTOR; EUROPEAN ASSOCIATION;
D O I
10.1016/j.jhep.2023.03.014
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The current document has been developed by the Liver Forum who mandated the NAFLD-Associated Comorbidities Working Group - a multistakeholder group comprised of experts from academic medicine, industry and patient associations - to identify aspects of diverse comorbidities frequently associated with non-alcoholic steatohepatitis (NASH) that can interfere with the conduct of therapeutic trials and, in particular, impact efficacy and safety results. The objective of this paper is to propose guidance for the management of relevant comorbidities in both candidates and actual participants in NASH therapeutic trials. We relied on specific guidelines from scientific societies, when available, but adapted them to the particulars of NASH trials with the aim of addressing multiple interacting requirements such as maintaining patient safety, reaching holistic therapeutic objectives, minimising confounding effects on efficacy and safety of investigational agents and allowing for trial completion. We divided the field of action into: first, analysis and stabilisation of the patient's condition before inclusion in the trial and, second, management of comorbidities during trial conduct. For the former, we discussed the concept of acceptable vs. optimal control of comorbidities, defined metabolic and ponderal stability prior to randomisation and weighed the pros and cons of a run-in period. For the latter, we analysed non-hepatological comorbid conditions for changes or acute events possibly occurring during the trial, including changes in alcohol consumption, in order to detail when specific interventions are necessary and how best to manage concomitant drug intake in line with methodological constraints. These recommendations are intended to act as a guide for clinical trialists and are open to further refinement when additional data become available. (c) 2023 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:829 / 841
页数:13
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