Mapping endocrine toxicity spectrum of immune checkpoint inhibitors: a disproportionality analysis using the WHO adverse drug reaction database, VigiBase

被引:48
作者
Bai, Xuefeng [1 ]
Lin, Xiahong [1 ,2 ]
Zheng, Kainan [3 ]
Chen, Xiaoyu [1 ]
Wu, Xiaohong [1 ]
Huang, Yinqiong [1 ]
Zhuang, Yong [1 ]
机构
[1] Fujian Med Univ, Affiliated Hosp 2, Dept Endocrinol, 950 Donghai St, Quanzhou, Fujian, Peoples R China
[2] Fujian Med Univ, Affiliated Hosp 2, Dept Med Adm, 950 Donghai St, Quanzhou, Fujian, Peoples R China
[3] China Telecom Co Ltd, Data Min Working Grp, Quanzhou Branch, 105 Citong Rd, Quanzhou, Fujian, Peoples R China
关键词
Immune checkpoint inhibitor; Endocrine toxicity; Endocrinopathy; Immune-related adverse event; Onset time; TYPE-1; DIABETES-MELLITUS; ANTI-CTLA-4; ANTIBODY; CANCER-IMMUNOTHERAPY; IPILIMUMAB; FULMINANT; MANAGEMENT; HYPOPHYSITIS; DYSFUNCTION; BLOCKADE; EVENTS;
D O I
10.1007/s12020-020-02355-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Purpose Our study aimed to map endocrine toxicity spectrum of immune checkpoint inhibitors (ICIs). Methods We obtained data from VigiBase, between January 1, 2011 and March 6, 2019. All endocrine adverse drug reactions (ADRs) were classified by group queries according to the Medical Dictionary for Regulatory Activities. Disproportionality analysis was performed with information component (IC) and reporting odds ratio (ROR). We used IC to identify meaningful endocrinopathies associated with ICIs and ROR to compare differences between ICI subgroups of ADRs. IC025(lower end of the 95% confidence interval of IC) is considered significant if larger than 0. Results In all, 6089 reports for endocrinopathies associated with ICIs were involved, with a male to female ratio of 1.5:1. The disproportionality analysis indicated significance of not only common endocrinopathies: thyroid dysfunction, hypophysitis/hypopituitarism, adrenal insufficiency, T1DM, fulminant T1DM (IC025: 4.12-6.62), but also rare endocrinopathies: hypoparathyroidism, diabetes insipidus, hypogonadism (IC025: 1.56-2.04). Increased risk of ADR reporting emerged in anti-CTLA-4 (e.g., hypophysitis/hypopituitarism, adrenal insufficiency) or in anti-PD-1/PD-L1 (e.g., thyroid dysfunction, T1DM, fulminant T1DM). In general, combination therapy (anti-CTLA-4 plus anti-PD-1/PD-L1) had a stronger association with endocrinopathies than monotherapy (ROR: 2.8, 95% CI: 2.5-3.1). Onset time of common endocrinopathies differed between different ICI therapies, typically within 12 weeks in anti-CTLA-4 monotherapy but diffusely ranging from 0 to 48 weeks in anti-PD-1 monotherapy. Conclusions Our study shows rising reporting frequencies of endocrinopathies caused by ICIs, especially aggravated in combination therapy. Clinicians should be early aware of latent endocrine toxicity and different onset time of endocrinopathies when implementing ICI therapies.
引用
收藏
页码:670 / 681
页数:12
相关论文
共 45 条
[31]  
Rastrelli M, 2014, IN VIVO, V28, P1005
[32]   Painless Thyroiditis and Fulminant Type 1 Diabetes Mellitus in a Patient Treated with an Immune Checkpoint Inhibitor, Nivolumab [J].
Sakurai, Kanako ;
Niitsuma, Satsuki ;
Sato, Ryota ;
Takahashi, Kazuhiro ;
Arihara, Zenei .
TOHOKU JOURNAL OF EXPERIMENTAL MEDICINE, 2018, 244 (01) :33-40
[33]   Cardiovascular toxicities associated with immune checkpoint inhibitors: an observational, retrospective, pharmacovigilance study [J].
Salem, Joe-Elie ;
Manouchehri, Ali ;
Moey, Melissa ;
Lebrun-Vignes, Benedicte ;
Bastarache, Lisa ;
Pariente, Antoine ;
Gobert, Aurelien ;
Spano, Jean-Philippe ;
Balko, Justin M. ;
Bonaca, Marc P. ;
Roden, Dan M. ;
Johnson, Douglas B. ;
Moslehi, Javid J. .
LANCET ONCOLOGY, 2018, 19 (12) :1579-1589
[34]   Fulminant Type 1 Diabetes Mellitus Accompanied by Positive Conversion of Anti-insulin Antibody after the Administration of Anti-CTLA-4 Antibody Following the Discontinuation of Anti-PD-1 Antibody [J].
Shiba, Michiru ;
Inaba, Hidefumi ;
Ariyasu, Hiroyuki ;
Kawai, Shintaro ;
Inagaki, Yuko ;
Matsuno, Shohei ;
Iwakura, Hiroshi ;
Yamamoto, Yuki ;
Nishi, Masahiro ;
Akamizu, Takashi .
INTERNAL MEDICINE, 2018, 57 (14) :2029-2034
[35]   Dermatologic Reactions to Immune Checkpoint Inhibitors Skin Toxicities and Immunotherapy [J].
Sibaud, Vincent .
AMERICAN JOURNAL OF CLINICAL DERMATOLOGY, 2018, 19 (03) :345-361
[36]   Management of toxicities of immune checkpoint inhibitors [J].
Spain, Lavinia ;
Diem, Stefan ;
Larkin, James .
CANCER TREATMENT REVIEWS, 2016, 44 :51-60
[37]   Collateral Damage: Insulin-Dependent Diabetes Induced With Checkpoint Inhibitors [J].
Stamatouli, Angeliki ;
Quandt, Zoe ;
Perdigoto, Ana Luisa ;
Clark, Pamela L. ;
Kluger, Harriet ;
Weiss, Sarah A. ;
Gettinger, Scott ;
Sznol, Mario ;
Young, Arabella ;
Rushakoff, Robert ;
Lee, James ;
Bluestone, Jeffrey A. ;
Anderson, Mark ;
Herold, Kevan C. .
DIABETES, 2018, 67 (08) :1471-1480
[38]   Endocrine-related adverse events associated with immune checkpoint blockade and expert insights on their management [J].
Sznol, Mario ;
Postow, Michael A. ;
Davies, Marianne J. ;
Pavlick, Anna C. ;
Plimack, Elizabeth R. ;
Shaheen, Montaser ;
Veloski, Colleen ;
Robert, Caroline .
CANCER TREATMENT REVIEWS, 2017, 58 :70-76
[39]   Thyroid Dysfunction as an Unintended Side Effect of Anticancer Drugs [J].
Torino, Francesco ;
Barnabei, Agnese ;
Paragliola, Rosamaria ;
Baldelli, Roberto ;
Appetecchia, Marialuisa ;
Corsello, Salvatore Maria .
THYROID, 2013, 23 (11) :1345-1366
[40]   Inflammation-induced hypoparathyroidism triggered by combination immune checkpoint blockade for melanoma [J].
Trinh, Beckey ;
Sanchez, Guacimara Ortega ;
Herzig, Petra ;
Laubli, Heinz .
JOURNAL FOR IMMUNOTHERAPY OF CANCER, 2019, 7