Anti-pituitary antibodies and susceptible human leukocyte antigen alleles as predictive biomarkers for pituitary dysfunction induced by immune checkpoint inhibitors

Background Pituitary dysfunction is a life-threatening immune-related adverse event (irAE) induced by immune checkpoint inhibitors (ICIs). To date, it is not possible to identify patients who may develop pituitary irAEs prior to ICI treatment. The aim of this study was to characterize the predisposi...

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Main Authors: Tomoko Kobayashi, Shintaro Iwama, Yoshinori Yasuda, Takayuki Okuji, Masaaki Ito, Takeshi Onoue, Mariko Sugiyama, Hiroshi Takagi, Daisuke Hagiwara, Yoshihiro Ito, Hidetaka Suga, Ryoichi Banno, Hiroshi Arima, Daisuke Sugiyama, Sachiko Ito
Format: Article
Language:English
Published: BMJ Publishing Group 2021-05-01
Series:Journal for ImmunoTherapy of Cancer
Online Access:https://jitc.bmj.com/content/9/5/e002493.full
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language English
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author Tomoko Kobayashi
Shintaro Iwama
Yoshinori Yasuda
Takayuki Okuji
Masaaki Ito
Takeshi Onoue
Mariko Sugiyama
Hiroshi Takagi
Daisuke Hagiwara
Yoshihiro Ito
Hidetaka Suga
Ryoichi Banno
Hiroshi Arima
Daisuke Sugiyama
Sachiko Ito
spellingShingle Tomoko Kobayashi
Shintaro Iwama
Yoshinori Yasuda
Takayuki Okuji
Masaaki Ito
Takeshi Onoue
Mariko Sugiyama
Hiroshi Takagi
Daisuke Hagiwara
Yoshihiro Ito
Hidetaka Suga
Ryoichi Banno
Hiroshi Arima
Daisuke Sugiyama
Sachiko Ito
Anti-pituitary antibodies and susceptible human leukocyte antigen alleles as predictive biomarkers for pituitary dysfunction induced by immune checkpoint inhibitors
Journal for ImmunoTherapy of Cancer
author_facet Tomoko Kobayashi
Shintaro Iwama
Yoshinori Yasuda
Takayuki Okuji
Masaaki Ito
Takeshi Onoue
Mariko Sugiyama
Hiroshi Takagi
Daisuke Hagiwara
Yoshihiro Ito
Hidetaka Suga
Ryoichi Banno
Hiroshi Arima
Daisuke Sugiyama
Sachiko Ito
author_sort Tomoko Kobayashi
title Anti-pituitary antibodies and susceptible human leukocyte antigen alleles as predictive biomarkers for pituitary dysfunction induced by immune checkpoint inhibitors
title_short Anti-pituitary antibodies and susceptible human leukocyte antigen alleles as predictive biomarkers for pituitary dysfunction induced by immune checkpoint inhibitors
title_full Anti-pituitary antibodies and susceptible human leukocyte antigen alleles as predictive biomarkers for pituitary dysfunction induced by immune checkpoint inhibitors
title_fullStr Anti-pituitary antibodies and susceptible human leukocyte antigen alleles as predictive biomarkers for pituitary dysfunction induced by immune checkpoint inhibitors
title_full_unstemmed Anti-pituitary antibodies and susceptible human leukocyte antigen alleles as predictive biomarkers for pituitary dysfunction induced by immune checkpoint inhibitors
title_sort anti-pituitary antibodies and susceptible human leukocyte antigen alleles as predictive biomarkers for pituitary dysfunction induced by immune checkpoint inhibitors
publisher BMJ Publishing Group
series Journal for ImmunoTherapy of Cancer
issn 2051-1426
publishDate 2021-05-01
description Background Pituitary dysfunction is a life-threatening immune-related adverse event (irAE) induced by immune checkpoint inhibitors (ICIs). To date, it is not possible to identify patients who may develop pituitary irAEs prior to ICI treatment. The aim of this study was to characterize the predisposition for ICI-induced pituitary irAEs by analyzing anti-pituitary antibodies (APAs) and human leukocyte antigens (HLAs).Methods In this case–control study, APAs and HLA alleles were analyzed in 62 patients (17 who developed ICI-induced isolated adrenocorticotropic hormone deficiency (ICI-IAD), 5 who developed ICI-induced hypophysitis (ICI-H) and 40 who did not develop pituitary irAEs) treated with ICIs between November 2, 2015, and March 31, 2020, at Nagoya University Hospital. The main outcome measures in this study were the association between the development of pituitary irAEs with APAs at baseline and after treatment and HLA alleles.Results Eleven of 17 (64.7%) patients who developed ICI-IAD had APAs at baseline, whereas APAs were positive only in 1 of 40 (2.5%) control patients. Although APAs were negative at baseline in all patients who developed ICI-H, they had become positive before the onset of ICI-H in 3 of 4 patients several weeks after ipilimumab administration. At the onset of ICI-IAD and ICI-H, APAs were positive in 15 of 17 (88.2%) and 4 of 5 (80%) patients, respectively. The prevalence of HLA-Cw12, HLA-DR15, HLA-DQ7, and HLA-DPw9 was significantly higher in patients with ICI-IAD, whereas that of HLA-Cw12 and HLA-DR15 was significantly higher in patients with ICI-H than in controls.Conclusions This study showed distinct and overlapped patterns of APAs and HLA alleles between ICI-IAD and ICI-H. Our findings also showed that positive APAs at baseline and after treatment, together with susceptible HLA alleles, could become predictive biomarkers for ICI-IAD and ICI-H, respectively.Trial registration number UMIN000019024.
url https://jitc.bmj.com/content/9/5/e002493.full
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spelling doaj-d2d9f49191b34aeab05ddd93407d12c42021-08-01T10:30:38ZengBMJ Publishing GroupJournal for ImmunoTherapy of Cancer2051-14262021-05-019510.1136/jitc-2021-002493Anti-pituitary antibodies and susceptible human leukocyte antigen alleles as predictive biomarkers for pituitary dysfunction induced by immune checkpoint inhibitorsTomoko Kobayashi0Shintaro Iwama1Yoshinori Yasuda2Takayuki Okuji3Masaaki Ito4Takeshi Onoue5Mariko Sugiyama6Hiroshi Takagi7Daisuke Hagiwara8Yoshihiro Ito9Hidetaka Suga10Ryoichi Banno11Hiroshi Arima12Daisuke Sugiyama13Sachiko Ito141 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan 1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan 1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan 1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan Department of Colorectal Surgery, National Cancer Center-Hospital East, Kashiwa, Chiba, Japan1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan 1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan 1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan 1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan Department of Anatomic Pathology, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan 1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan 1 Department of Endocrinology and Diabetes, Nagoya University Graduate School of Medicine, Nagoya, Japan 1 Department of Preventive Medicine and Public Health, Keio University School of Medicine, Shinjuku, Tokyo, Japan Department of Immunology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, JapanBackground Pituitary dysfunction is a life-threatening immune-related adverse event (irAE) induced by immune checkpoint inhibitors (ICIs). To date, it is not possible to identify patients who may develop pituitary irAEs prior to ICI treatment. The aim of this study was to characterize the predisposition for ICI-induced pituitary irAEs by analyzing anti-pituitary antibodies (APAs) and human leukocyte antigens (HLAs).Methods In this case–control study, APAs and HLA alleles were analyzed in 62 patients (17 who developed ICI-induced isolated adrenocorticotropic hormone deficiency (ICI-IAD), 5 who developed ICI-induced hypophysitis (ICI-H) and 40 who did not develop pituitary irAEs) treated with ICIs between November 2, 2015, and March 31, 2020, at Nagoya University Hospital. The main outcome measures in this study were the association between the development of pituitary irAEs with APAs at baseline and after treatment and HLA alleles.Results Eleven of 17 (64.7%) patients who developed ICI-IAD had APAs at baseline, whereas APAs were positive only in 1 of 40 (2.5%) control patients. Although APAs were negative at baseline in all patients who developed ICI-H, they had become positive before the onset of ICI-H in 3 of 4 patients several weeks after ipilimumab administration. At the onset of ICI-IAD and ICI-H, APAs were positive in 15 of 17 (88.2%) and 4 of 5 (80%) patients, respectively. The prevalence of HLA-Cw12, HLA-DR15, HLA-DQ7, and HLA-DPw9 was significantly higher in patients with ICI-IAD, whereas that of HLA-Cw12 and HLA-DR15 was significantly higher in patients with ICI-H than in controls.Conclusions This study showed distinct and overlapped patterns of APAs and HLA alleles between ICI-IAD and ICI-H. Our findings also showed that positive APAs at baseline and after treatment, together with susceptible HLA alleles, could become predictive biomarkers for ICI-IAD and ICI-H, respectively.Trial registration number UMIN000019024.https://jitc.bmj.com/content/9/5/e002493.full