Efficacy and safety of mycophenolate mofetil in treating immune-related hepatitis induced by immune checkpoint inhibitor use: A retrospective study.

hepatitis immune checkpoint inhibitor immune‐related adverse event mycophenolate mofetil

Journal

JGH open : an open access journal of gastroenterology and hepatology
ISSN: 2397-9070
Titre abrégé: JGH Open
Pays: Australia
ID NLM: 101730833

Informations de publication

Date de publication:
Feb 2023
Historique:
received: 04 09 2022
revised: 17 12 2022
accepted: 12 01 2023
entrez: 28 2 2023
pubmed: 1 3 2023
medline: 1 3 2023
Statut: epublish

Résumé

To investigate the outcomes in eight Japanese patients with cancer treated with mycophenolate mofetil (MMF) and corticosteroids for immune checkpoint inhibitor treatment-induced severe immune-related hepatitis (ir-hepatitis) and the efficacy and safety of MMF. We retrospectively examined patient background, treatment course, as well as examination and imaging data using electronic medical records. The ratio of male to female patients was 7:1, and the median age was 60 years (27-72 years). There were five and two cases of kidney cancer and malignant melanoma, respectively, and one case of lung cancer. The median number of days until MMF administration in addition to systemic corticosteroid therapy after the onset of ir-hepatitis was 14.5 (2-42). The patients were categorized as four "good responders" who showed an improvement in the liver function tests following MMF treatment and four "poor responders" who did not. Furthermore, the time from the onset of ir-hepatitis to initial MMF administration was significantly shorter in good responders (median 3 days, range 2-15 days) than in poor responders (median 25.5 days, range 14-42 days) ( According to these findings, early recognition of corticosteroid refractoriness and the use of MMF may be beneficial in patients with ir-hepatitis.

Sections du résumé

Background and Aim UNASSIGNED
To investigate the outcomes in eight Japanese patients with cancer treated with mycophenolate mofetil (MMF) and corticosteroids for immune checkpoint inhibitor treatment-induced severe immune-related hepatitis (ir-hepatitis) and the efficacy and safety of MMF.
Methods UNASSIGNED
We retrospectively examined patient background, treatment course, as well as examination and imaging data using electronic medical records.
Results UNASSIGNED
The ratio of male to female patients was 7:1, and the median age was 60 years (27-72 years). There were five and two cases of kidney cancer and malignant melanoma, respectively, and one case of lung cancer. The median number of days until MMF administration in addition to systemic corticosteroid therapy after the onset of ir-hepatitis was 14.5 (2-42). The patients were categorized as four "good responders" who showed an improvement in the liver function tests following MMF treatment and four "poor responders" who did not. Furthermore, the time from the onset of ir-hepatitis to initial MMF administration was significantly shorter in good responders (median 3 days, range 2-15 days) than in poor responders (median 25.5 days, range 14-42 days) (
Conclusions UNASSIGNED
According to these findings, early recognition of corticosteroid refractoriness and the use of MMF may be beneficial in patients with ir-hepatitis.

Identifiants

pubmed: 36852148
doi: 10.1002/jgh3.12868
pii: JGH312868
pmc: PMC9958334
doi:

Types de publication

Journal Article

Langues

eng

Pagination

87-97

Informations de copyright

© 2023 The Authors. JGH Open published by Journal of Gastroenterology and Hepatology Foundation and John Wiley & Sons Australia, Ltd.

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Auteurs

Yukio Kadokawa (Y)

Department of Pharmacy Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Satoko Inoue (S)

Department of Pharmacy Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Akitoshi Tatsumi (A)

Faculty of Pharmaceutical Sciences Kobe Gakuin University Kobe Japan.

Mayako Uchida (M)

Faculty of Pharmaceutical Sciences Doshisha Women's College of Liberal Arts Kyoto Japan.

Keiko Fujita (K)

Department of Pharmacy Osaka General Medical Center, Osaka Prefectural Hospital Organization Osaka Japan.

Mari Takagi (M)

Department of Pharmacy Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Takako Inoue (T)

Department of Respiratory Medicine Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Shuichi Ohe (S)

Department of Dermatologic Oncology Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Yasutomo Nakai (Y)

Department of Urology Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Tomoyuki Otsuka (T)

Department of Medical Oncology Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Yutaro Abe (Y)

Department of Hepatobiliary and Pancreatic Oncology Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Tasuku Nakabori (T)

Department of Hepatobiliary and Pancreatic Oncology Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Taiki Isei (T)

Department of Dermatologic Oncology Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Toru Kumagai (T)

Department of Respiratory Medicine Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Kazuo Nishimura (K)

Department of Urology Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Kazuyoshi Ohkawa (K)

Department of Hepatobiliary and Pancreatic Oncology Osaka International Cancer Institute, Osaka Prefectural Hospital Organization Osaka Japan.

Classifications MeSH