Real-World Evidence of the Incidence of and Risk Factors for Type 1 Diabetes Mellitus and Hypothyroidism as Immune-Related Adverse Events Associated With Programmed Cell Death-1 Inhibitors.


Journal

Endocrine practice : official journal of the American College of Endocrinology and the American Association of Clinical Endocrinologists
ISSN: 1530-891X
Titre abrégé: Endocr Pract
Pays: United States
ID NLM: 9607439

Informations de publication

Date de publication:
Jun 2021
Historique:
received: 14 10 2020
revised: 09 12 2020
accepted: 12 12 2020
pubmed: 1 6 2021
medline: 16 6 2021
entrez: 31 5 2021
Statut: ppublish

Résumé

The incidence of type 1 diabetes mellitus (T1DM) and hypothyroidism as immune-related adverse events (irAEs) after programmed cell death-1 inhibitor (PD-1i) administration has not yet been sufficiently evaluated in a real clinical setting. To assess the incidence of T1DM and hypothyroidism among PD-1is and to identify the risk factors associated with hypothyroidism using a large claims database. This cohort study used the Shizuoka Kokuho database in Japan from 2012 to 2018, including approximately 2.2 million people. We enrolled 695 PD-1i-treated patients. T1DM and hypothyroidism as irAEs were identified using International Classification of Diseases 10th Revision and Anatomical Therapeutic Chemical classification codes. Risk factors for hypothyroidism were explored using the multivariable Fine and Gray regression model after adjusting for age group and sex, treating death as a competing risk. The cumulative incidences of T1DM and hypothyroidism were 0.3% and 8.3%, respectively. We described the detailed onset timing of irAEs in patients with T1DM and hypothyroidism; hypothyroidism was observed evenly within 1 year of the PD-1i prescription. Sex and certain cancer types, such as lung and urothelial cancers, were significantly associated with subdistribution hazard ratio (sHR) (female: sHR, 2.04 [95% CI, 1.20-3.47]; lung cancer: sHR, 0.55 [95% CI, 0.32-0.95]; and urothelial carcinoma: sHR, 2.40 [95% CI, 1.05-5.49]). The incidence of T1DM and hypothyroidism as irAEs and associated risk factors identified in this analysis were comparable to those found in previous studies. The use of a large claims database to detect irAEs, such as T1DM and hypothyroidism, may lead to safer use of PD-1is.

Identifiants

pubmed: 34057406
pii: S1530-891X(20)48432-0
doi: 10.1016/j.eprac.2020.12.009
pii:
doi:

Substances chimiques

Programmed Cell Death 1 Receptor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

586-593

Informations de copyright

Copyright © 2020 AACE. Published by Elsevier Inc. All rights reserved.

Auteurs

Koki Shimada (K)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan; Department of Health Policy and Management, School of Medicine, Keio University, Tokyo, Japan.

Hiroyuki Yamamoto (H)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan; Department of Health Policy and Management, School of Medicine, Keio University, Tokyo, Japan. Electronic address: yama-h@umin.ac.jp.

Eiji Nakatani (E)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan.

Hiraku Kumamaru (H)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan; Department of Healthcare Quality Assessment, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Shiori Nishimura (S)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan; Department of Health Policy and Management, School of Medicine, Keio University, Tokyo, Japan.

Nao Ichihara (N)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan; Department of Healthcare Quality Assessment, Graduate School of Medicine, The University of Tokyo, Tokyo, Japan.

Norimichi Hirahara (N)

Department of Health Policy and Management, School of Medicine, Keio University, Tokyo, Japan.

Kiyoshi Mori (K)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan.

Masato Kotani (M)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan.

Yoshiki Miyachi (Y)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan.

Hiroaki Miyata (H)

Research Support Center, Shizuoka General Hospital, Shizuoka, Japan; Department of Health Policy and Management, School of Medicine, Keio University, Tokyo, Japan.

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