TY - JOUR
T1 - 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
AU - Shimada, Koki
AU - Yamamoto, Hiroyuki
AU - Nakatani, Eiji
AU - Kumamaru, Hiraku
AU - Nishimura, Shiori
AU - Ichihara, Nao
AU - Hirahara, Norimichi
AU - Mori, Kiyoshi
AU - Kotani, Masato
AU - Miyachi, Yoshiki
AU - Miyata, Hiroaki
N1 - Funding Information:
We thank the Research Support Center in Shizuoka General Hospital for conducting contract research projects related to public health in Shizuoka prefecture, including this study (2020-11). K.S. H.Y. H.K. S.N. and H.M. contributed to the conceptualization and methodology; K.S. and H.Y. conducted the formal analysis and visualization; K.S. H.Y. E.N. and S.N. contributed to the data curation; Y.M. and H.M. contributed to the funding acquisition; H.Y. and H.M. managed the project administration; and K.S. H.Y. and H.M. drafted the writing of the original manuscript. All authors contributed substantially to the interpretation of results and writing, review, and editing of the final draft. K.S. H.Y. H.K. S.N. N.I. N.H. and H.M. are affiliated with the Department of Healthcare Quality Assessment at The University of Tokyo. The department is a social collaboration department supported by grants from the National Clinical Database, Johnson & Johnson K.K. and Nipro Corporation. K.S. reports receiving a portion of his salary from joint research funding by AstraZeneca K.K. of the JST-OPERA Program. H.Y. has received a consultation fee from Mitsubishi Tanabe Pharma, speaker fee from Chugai Pharmaceutical Co. Ltd. and Ono Pharmaceutical Co. Ltd. and payment for a manuscript from Astellas Pharma Inc. H.K. has received a consultation fee from Mitsubishi Tanabe Pharma and a lecture fee from Pfizer Japan, Inc.
Funding Information:
K.S., H.Y., H.K., S.N., N.I., N.H., and H.M. are affiliated with the Department of Healthcare Quality Assessment at The University of Tokyo. The department is a social collaboration department supported by grants from the National Clinical Database, Johnson & Johnson K.K., and Nipro Corporation. K.S. reports receiving a portion of his salary from joint research funding by AstraZeneca K.K. of the JST-OPERA Program. H.Y. has received a consultation fee from Mitsubishi Tanabe Pharma, speaker fee from Chugai Pharmaceutical Co., Ltd. and Ono Pharmaceutical Co., Ltd., and payment for a manuscript from Astellas Pharma Inc. H.K. has received a consultation fee from Mitsubishi Tanabe Pharma and a lecture fee from Pfizer Japan, Inc.
Publisher Copyright:
© 2020 AACE
PY - 2021/6
Y1 - 2021/6
N2 - Objective: 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. Methods: 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. Results: 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]). Conclusion: 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.
AB - Objective: 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. Methods: 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. Results: 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]). Conclusion: 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.
KW - claims data
KW - hypothyroidism
KW - immune-related adverse events
KW - risk factors
KW - type 1 diabetes
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U2 - 10.1016/j.eprac.2020.12.009
DO - 10.1016/j.eprac.2020.12.009
M3 - Article
C2 - 34057406
AN - SCOPUS:85108302683
SN - 1530-891X
VL - 27
SP - 586
EP - 593
JO - Endocrine Practice
JF - Endocrine Practice
IS - 6
ER -