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Combination Therapy With Tofacitinib Plus Intensive Granulocyte and Monocyte Adsorptive Apheresis as Induction Therapy for Refractory Ulcerative Colitis

BACKGROUND: The use of monotherapy with intensive granulocyte and monocyte adsorptive apheresis (GMA) or a Janus kinase (JAK) inhibitor has been limited to patients with refractory ulcerative colitis (UC). The efficacy and safety of combination therapy with tofacitinib (TOF) plus intensive GMA (two...

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Autores principales: Tanida, Satoshi, Ozeki, Keiji, Mizoshita, Tsutomu, Kitagawa, Mika, Ozeki, Takanori, Tanaka, Mamoru, Nishie, Hirotada, Shimura, Takaya, Kubota, Eiji, Kataoka, Hiromi
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elmer Press 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968921/
https://www.ncbi.nlm.nih.gov/pubmed/32010420
http://dx.doi.org/10.14740/jocmr4037
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author Tanida, Satoshi
Ozeki, Keiji
Mizoshita, Tsutomu
Kitagawa, Mika
Ozeki, Takanori
Tanaka, Mamoru
Nishie, Hirotada
Shimura, Takaya
Kubota, Eiji
Kataoka, Hiromi
author_facet Tanida, Satoshi
Ozeki, Keiji
Mizoshita, Tsutomu
Kitagawa, Mika
Ozeki, Takanori
Tanaka, Mamoru
Nishie, Hirotada
Shimura, Takaya
Kubota, Eiji
Kataoka, Hiromi
author_sort Tanida, Satoshi
collection PubMed
description BACKGROUND: The use of monotherapy with intensive granulocyte and monocyte adsorptive apheresis (GMA) or a Janus kinase (JAK) inhibitor has been limited to patients with refractory ulcerative colitis (UC). The efficacy and safety of combination therapy with tofacitinib (TOF) plus intensive GMA (two sessions per week) for refractory UC have not been evaluated. METHODS: This retrospective study evaluated the 10-week efficacy of combination therapy with TOF plus intensive GMA in patients with refractory UC. RESULTS: Of seven patients who received a combination therapy with TOF plus intensive GMA, 71.4% achieved clinical remission at 10 weeks. The percentages of patients with mucosal healing and complete mucosal healing at 10 weeks were 100% and 42.9%, respectively. The mean full Mayo score and endoscopic subscore at baseline were 8.71 ± 0.80 and 2.4 ± 0.2, respectively, and the corresponding values at 10 weeks were 1.57 ± 0.48 and 0.6 ± 0.2 (P < 0.01), respectively. Adverse events of an orolabial herpes and temporary increase in creatinine phosphokinase (CK) and triglyceride were observed in three patients. CONCLUSIONS: Based on these outcomes, combination therapy with TOF plus intensive GMA was well tolerated and may be useful for induction of clinical remission in patients with refractory UC.
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spelling pubmed-69689212020-01-31 Combination Therapy With Tofacitinib Plus Intensive Granulocyte and Monocyte Adsorptive Apheresis as Induction Therapy for Refractory Ulcerative Colitis Tanida, Satoshi Ozeki, Keiji Mizoshita, Tsutomu Kitagawa, Mika Ozeki, Takanori Tanaka, Mamoru Nishie, Hirotada Shimura, Takaya Kubota, Eiji Kataoka, Hiromi J Clin Med Res Short Communication BACKGROUND: The use of monotherapy with intensive granulocyte and monocyte adsorptive apheresis (GMA) or a Janus kinase (JAK) inhibitor has been limited to patients with refractory ulcerative colitis (UC). The efficacy and safety of combination therapy with tofacitinib (TOF) plus intensive GMA (two sessions per week) for refractory UC have not been evaluated. METHODS: This retrospective study evaluated the 10-week efficacy of combination therapy with TOF plus intensive GMA in patients with refractory UC. RESULTS: Of seven patients who received a combination therapy with TOF plus intensive GMA, 71.4% achieved clinical remission at 10 weeks. The percentages of patients with mucosal healing and complete mucosal healing at 10 weeks were 100% and 42.9%, respectively. The mean full Mayo score and endoscopic subscore at baseline were 8.71 ± 0.80 and 2.4 ± 0.2, respectively, and the corresponding values at 10 weeks were 1.57 ± 0.48 and 0.6 ± 0.2 (P < 0.01), respectively. Adverse events of an orolabial herpes and temporary increase in creatinine phosphokinase (CK) and triglyceride were observed in three patients. CONCLUSIONS: Based on these outcomes, combination therapy with TOF plus intensive GMA was well tolerated and may be useful for induction of clinical remission in patients with refractory UC. Elmer Press 2020-01 2020-01-06 /pmc/articles/PMC6968921/ /pubmed/32010420 http://dx.doi.org/10.14740/jocmr4037 Text en Copyright 2020, Tanida et al. http://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution Non-Commercial 4.0 International License, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Short Communication
Tanida, Satoshi
Ozeki, Keiji
Mizoshita, Tsutomu
Kitagawa, Mika
Ozeki, Takanori
Tanaka, Mamoru
Nishie, Hirotada
Shimura, Takaya
Kubota, Eiji
Kataoka, Hiromi
Combination Therapy With Tofacitinib Plus Intensive Granulocyte and Monocyte Adsorptive Apheresis as Induction Therapy for Refractory Ulcerative Colitis
title Combination Therapy With Tofacitinib Plus Intensive Granulocyte and Monocyte Adsorptive Apheresis as Induction Therapy for Refractory Ulcerative Colitis
title_full Combination Therapy With Tofacitinib Plus Intensive Granulocyte and Monocyte Adsorptive Apheresis as Induction Therapy for Refractory Ulcerative Colitis
title_fullStr Combination Therapy With Tofacitinib Plus Intensive Granulocyte and Monocyte Adsorptive Apheresis as Induction Therapy for Refractory Ulcerative Colitis
title_full_unstemmed Combination Therapy With Tofacitinib Plus Intensive Granulocyte and Monocyte Adsorptive Apheresis as Induction Therapy for Refractory Ulcerative Colitis
title_short Combination Therapy With Tofacitinib Plus Intensive Granulocyte and Monocyte Adsorptive Apheresis as Induction Therapy for Refractory Ulcerative Colitis
title_sort combination therapy with tofacitinib plus intensive granulocyte and monocyte adsorptive apheresis as induction therapy for refractory ulcerative colitis
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6968921/
https://www.ncbi.nlm.nih.gov/pubmed/32010420
http://dx.doi.org/10.14740/jocmr4037
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