TY - JOUR
T1 - Systematic review of response criteria and endpoints in autoimmune hepatitis by the International Autoimmune Hepatitis Group
AU - Pape, Simon
AU - Snijders, Romée J. A. L. M.
AU - Gevers, Tom J. G.
AU - Chazouilleres, Oliver
AU - Dalekos, George N.
AU - Hirschfield, Gideon M.
AU - Lenzi, Marco
AU - Trauner, Michael
AU - Manns, Michael P.
AU - Vierling, John M.
AU - Montano-Loza, Aldo J.
AU - Lohse, Ansgar W.
AU - Schramm, Christoph
AU - Drenth, Joost P. H.
AU - Heneghan, Michael A.
AU - International Autoimmune Hepatitis Group (IAIHG) collaborators‡
AU - Almasio, P.
AU - Alvarez, F.
AU - Andrade, R.
AU - Arikan, C.
AU - Assis, D.
AU - Bardou-Jacquet, E.
AU - Biewenga, M.
AU - Cancado, E.
AU - Cazzagon, N.
AU - Chazouillères, O.
AU - Colloredo, G.
AU - Cuarterolo, M.
AU - Dalekos, G.
AU - Debray, D.
AU - Robles-Díaz, M.
AU - Drenth, J.
AU - Dyson, J.
AU - Efe, C.
AU - Engel, B.
AU - Ferri, S.
AU - Fontana, R.
AU - Gatselis, N.
AU - Gerussi, A.
AU - Halilbasic, E.
AU - Halliday, N.
AU - Heneghan, M.
AU - Hirschfield, G.
AU - van Hoek, B.
AU - Hørby Jørgensen, M.
AU - Indolfini, G.
AU - Iorio, R.
AU - Jeong, S.
AU - Jones, D.
AU - van Nieuwkerk, C.
AU - van den Brand, F.
N1 - Funding Information: This IAIHG meeting (July 2019) was supported by the YAEL Foundation . This work has been generated within the European Reference Network on Hepatological Diseases (ERN RARE-LIVER) . Publisher Copyright: © 2022 The Authors
PY - 2022/4/1
Y1 - 2022/4/1
N2 - Background & Aims: Autoimmune hepatitis (AIH) has been well characterised and codified through the development of diagnostic criteria. These criteria have been adapted and simplified and are widely used in clinical practice. However, there is a need to update and precisely define the criteria for both treatment response and treatment. Methods: A systematic review was performed and a modified Delphi consensus process was used to identify and redefine the response criteria in autoimmune hepatitis. Results: The consensus process initiated by the International Autoimmune Hepatitis Group proposes that the term ‘complete biochemical response’ defined as ‘normalization of serum transaminases and IgG below the upper limit of normal’ be adopted to include a time point at 6 months after initiation of treatment. An insufficient response by 6 months was a failure to meet the above definition. Non-response was defined as ‘<50% decrease of serum transaminases within 4 weeks after initiation of treatment’. Remission is defined as liver histology with a Hepatitis Activity Index <4/18. Intolerance to treatment was agreed to stand for ‘any adverse event possibly related to treatment leading to potential drug discontinuation’. Conclusions: These definitions provide a simple and reproducible framework to define treatment response and non-response, irrespective of the therapeutic intervention. A consensus on endpoints is urgently required to set a global standard for the reporting of study results and to enable inter-study comparisons. Future prospective database studies are needed to validate these endpoints. Lay summary: Consensus among international experts on response criteria and endpoints in autoimmune hepatitis is lacking. A consensus on endpoints is urgently required to set a global standard for the reporting of study results and to enable the comparison of results between clinical trials. Therefore, the International Autoimmune Hepatitis Group (IAIHG) herein presents a statement on 5 agreed response criteria and endpoints: complete biochemical response, insufficient response, non-response, remission, and intolerance to treatment, which can be used to guide future reporting.
AB - Background & Aims: Autoimmune hepatitis (AIH) has been well characterised and codified through the development of diagnostic criteria. These criteria have been adapted and simplified and are widely used in clinical practice. However, there is a need to update and precisely define the criteria for both treatment response and treatment. Methods: A systematic review was performed and a modified Delphi consensus process was used to identify and redefine the response criteria in autoimmune hepatitis. Results: The consensus process initiated by the International Autoimmune Hepatitis Group proposes that the term ‘complete biochemical response’ defined as ‘normalization of serum transaminases and IgG below the upper limit of normal’ be adopted to include a time point at 6 months after initiation of treatment. An insufficient response by 6 months was a failure to meet the above definition. Non-response was defined as ‘<50% decrease of serum transaminases within 4 weeks after initiation of treatment’. Remission is defined as liver histology with a Hepatitis Activity Index <4/18. Intolerance to treatment was agreed to stand for ‘any adverse event possibly related to treatment leading to potential drug discontinuation’. Conclusions: These definitions provide a simple and reproducible framework to define treatment response and non-response, irrespective of the therapeutic intervention. A consensus on endpoints is urgently required to set a global standard for the reporting of study results and to enable inter-study comparisons. Future prospective database studies are needed to validate these endpoints. Lay summary: Consensus among international experts on response criteria and endpoints in autoimmune hepatitis is lacking. A consensus on endpoints is urgently required to set a global standard for the reporting of study results and to enable the comparison of results between clinical trials. Therefore, the International Autoimmune Hepatitis Group (IAIHG) herein presents a statement on 5 agreed response criteria and endpoints: complete biochemical response, insufficient response, non-response, remission, and intolerance to treatment, which can be used to guide future reporting.
KW - autoimmune hepatitis
KW - complete biochemical response
KW - endpoints
KW - insufficient response
KW - intolerance
KW - non-response
KW - remission
UR - http://www.scopus.com/inward/record.url?scp=85124827323&partnerID=8YFLogxK
U2 - https://doi.org/10.1016/j.jhep.2021.12.041
DO - https://doi.org/10.1016/j.jhep.2021.12.041
M3 - Article
C2 - 35066089
SN - 0168-8278
VL - 76
SP - 841
EP - 849
JO - Journal of Hepatology
JF - Journal of Hepatology
IS - 4
ER -