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Profiling the patient with autoimmune hepatitis on calcineurin inhibitors: a real-world-experience

OBJECTIVE: Therapy for autoimmune hepatitis (AIH) consists of steroid induction therapy, followed by maintenance therapy with azathioprine. However, up to 20% of patients experience either insufficient response or intolerance on first-line therapy. Calcineurin inhibitors (CNIs) are frequently used w...

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Autores principales: Pape, Simon, Nevens, Frederik, Verslype, Chris, Mertens, Caroline, Drenth, Joost P.H., Tjwa, Eric T.T.L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams And Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195854/
https://www.ncbi.nlm.nih.gov/pubmed/31658173
http://dx.doi.org/10.1097/MEG.0000000000001580
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author Pape, Simon
Nevens, Frederik
Verslype, Chris
Mertens, Caroline
Drenth, Joost P.H.
Tjwa, Eric T.T.L.
author_facet Pape, Simon
Nevens, Frederik
Verslype, Chris
Mertens, Caroline
Drenth, Joost P.H.
Tjwa, Eric T.T.L.
author_sort Pape, Simon
collection PubMed
description OBJECTIVE: Therapy for autoimmune hepatitis (AIH) consists of steroid induction therapy, followed by maintenance therapy with azathioprine. However, up to 20% of patients experience either insufficient response or intolerance on first-line therapy. Calcineurin inhibitors (CNIs) are frequently used when first-line therapy fails. Although a number of studies report on efficacy, less is known on the patient trajectory before switch to CNIs. Our aim was to describe the road toward CNI therapy in AIH patients. METHODS: Patients with an AIH diagnosis who used CNIs as either second- or third-line treatment were included in the study. Reason for switch to CNI was assessed as either an insufficient response or intolerance to prior therapy. Efficacy was assessed by normalization of transaminases at last moment of follow-up. RESULTS: Final analysis included 20 patients who were treated with CNIs. Ten patients were treated with tacrolimus and ten patients received cyclosporine. In patients who used CNI treatment as third-line therapy (n = 13), duration of first-line therapy was almost twice as long as duration of second-line therapy (2.58 years vs. 1.33 years; P = 0.67). Patients treated with tacrolimus had relatively high trough levels (7.6 ng/mL) and more (minor) adverse events. Fifty-five percent of patients had normalization of transaminases at last moment of follow-up. CONCLUSION: CNI treatment in AIH as second- or third-line therapy is effective in ~50% of patients. The trajectory before switch varies considerably between patients.
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spelling pubmed-71958542020-05-21 Profiling the patient with autoimmune hepatitis on calcineurin inhibitors: a real-world-experience Pape, Simon Nevens, Frederik Verslype, Chris Mertens, Caroline Drenth, Joost P.H. Tjwa, Eric T.T.L. Eur J Gastroenterol Hepatol Original Articles: Hepatology OBJECTIVE: Therapy for autoimmune hepatitis (AIH) consists of steroid induction therapy, followed by maintenance therapy with azathioprine. However, up to 20% of patients experience either insufficient response or intolerance on first-line therapy. Calcineurin inhibitors (CNIs) are frequently used when first-line therapy fails. Although a number of studies report on efficacy, less is known on the patient trajectory before switch to CNIs. Our aim was to describe the road toward CNI therapy in AIH patients. METHODS: Patients with an AIH diagnosis who used CNIs as either second- or third-line treatment were included in the study. Reason for switch to CNI was assessed as either an insufficient response or intolerance to prior therapy. Efficacy was assessed by normalization of transaminases at last moment of follow-up. RESULTS: Final analysis included 20 patients who were treated with CNIs. Ten patients were treated with tacrolimus and ten patients received cyclosporine. In patients who used CNI treatment as third-line therapy (n = 13), duration of first-line therapy was almost twice as long as duration of second-line therapy (2.58 years vs. 1.33 years; P = 0.67). Patients treated with tacrolimus had relatively high trough levels (7.6 ng/mL) and more (minor) adverse events. Fifty-five percent of patients had normalization of transaminases at last moment of follow-up. CONCLUSION: CNI treatment in AIH as second- or third-line therapy is effective in ~50% of patients. The trajectory before switch varies considerably between patients. Lippincott Williams And Wilkins 2020-06 2019-10-02 /pmc/articles/PMC7195854/ /pubmed/31658173 http://dx.doi.org/10.1097/MEG.0000000000001580 Text en Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-No Derivatives License 4.0 (http://creativecommons.org/licenses/by-nc-nd/4.0/) (CC-BY-NC-ND), where it is permissible to download and share the work provided it is properly cited. The work cannot be changed in any way or used commercially without permission from the journal.
spellingShingle Original Articles: Hepatology
Pape, Simon
Nevens, Frederik
Verslype, Chris
Mertens, Caroline
Drenth, Joost P.H.
Tjwa, Eric T.T.L.
Profiling the patient with autoimmune hepatitis on calcineurin inhibitors: a real-world-experience
title Profiling the patient with autoimmune hepatitis on calcineurin inhibitors: a real-world-experience
title_full Profiling the patient with autoimmune hepatitis on calcineurin inhibitors: a real-world-experience
title_fullStr Profiling the patient with autoimmune hepatitis on calcineurin inhibitors: a real-world-experience
title_full_unstemmed Profiling the patient with autoimmune hepatitis on calcineurin inhibitors: a real-world-experience
title_short Profiling the patient with autoimmune hepatitis on calcineurin inhibitors: a real-world-experience
title_sort profiling the patient with autoimmune hepatitis on calcineurin inhibitors: a real-world-experience
topic Original Articles: Hepatology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7195854/
https://www.ncbi.nlm.nih.gov/pubmed/31658173
http://dx.doi.org/10.1097/MEG.0000000000001580
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