Endocrine toxicity of immune checkpoint inhibitors: a network meta-analysis of the current evidence

Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment but pose a challenge of immune-related adverse events (irAEs), particularly endocrine toxicity, that can severely compromise patient well-being. Existing research has often been limited in scope and has not provided comprehensi...

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Main Authors: Peipei Ouyang, Weiting Yang, Jianqiao Sun, Ping Chen, Qingyun He, Jiaxin Yan, Wenhao Wang, Yi Wang, Heran Li, Qiuhua Luo
Format: Article
Language:English
Published: Compuscript Ltd 2024-01-01
Series:Acta Materia Medica
Online Access:https://www.scienceopen.com/hosted-document?doi=10.15212/AMM-2023-0037
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author Peipei Ouyang
Weiting Yang
Jianqiao Sun
Ping Chen
Qingyun He
Jiaxin Yan
Wenhao Wang
Yi Wang
Heran Li
Qiuhua Luo
author_facet Peipei Ouyang
Weiting Yang
Jianqiao Sun
Ping Chen
Qingyun He
Jiaxin Yan
Wenhao Wang
Yi Wang
Heran Li
Qiuhua Luo
author_sort Peipei Ouyang
collection DOAJ
description Immune checkpoint inhibitors (ICIs) have revolutionized cancer treatment but pose a challenge of immune-related adverse events (irAEs), particularly endocrine toxicity, that can severely compromise patient well-being. Existing research has often been limited in scope and has not provided comprehensive safety profiles across the diverse range of ICI therapies. We addressed this gap by performing a network meta-analysis on 55 randomized controlled trials involving 32,522 patients. Using STATA to calculate the surface under the cumulative ranking curve, we ranked the safety of various ICI monotherapies and combination therapies. ICIs were found to increase the risk of endocrine toxicities, such as hypothyroidism, hyperthyroidism, hypophysitis, thyroiditis, and adrenal insufficiency; this risk was greater with dual ICI regimens. Specifically, cytotoxic T lymphocyte associated antigen-4 (CTLA-4) inhibitors, such as ipilimumab, are closely associated with hypophysitis, whereas programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1) inhibitors, notably pembrolizumab and nivolumab, predispose patients to thyroid-related dysfunction, such as hyperthyroidism, hypothyroidism, and thyroiditis. Interestingly, nivolumab showed no elevated risk of adrenal dysfunction, in contrast to the elevated risk observed with other ICI treatments. This study provides critical evidence-based insights for optimizing the risk-benefit balance of ICI therapies in clinical practice.
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spelling doaj.art-a828679a486742c29b11a82a062f71842024-03-02T17:00:12ZengCompuscript LtdActa Materia Medica2737-79462024-01-013111910.15212/AMM-2023-0037Endocrine toxicity of immune checkpoint inhibitors: a network meta-analysis of the current evidencePeipei OuyangWeiting YangJianqiao SunPing ChenQingyun HeJiaxin YanWenhao WangYi WangHeran LiQiuhua LuoImmune checkpoint inhibitors (ICIs) have revolutionized cancer treatment but pose a challenge of immune-related adverse events (irAEs), particularly endocrine toxicity, that can severely compromise patient well-being. Existing research has often been limited in scope and has not provided comprehensive safety profiles across the diverse range of ICI therapies. We addressed this gap by performing a network meta-analysis on 55 randomized controlled trials involving 32,522 patients. Using STATA to calculate the surface under the cumulative ranking curve, we ranked the safety of various ICI monotherapies and combination therapies. ICIs were found to increase the risk of endocrine toxicities, such as hypothyroidism, hyperthyroidism, hypophysitis, thyroiditis, and adrenal insufficiency; this risk was greater with dual ICI regimens. Specifically, cytotoxic T lymphocyte associated antigen-4 (CTLA-4) inhibitors, such as ipilimumab, are closely associated with hypophysitis, whereas programmed cell death-1 (PD-1)/programmed cell death ligand-1 (PD-L1) inhibitors, notably pembrolizumab and nivolumab, predispose patients to thyroid-related dysfunction, such as hyperthyroidism, hypothyroidism, and thyroiditis. Interestingly, nivolumab showed no elevated risk of adrenal dysfunction, in contrast to the elevated risk observed with other ICI treatments. This study provides critical evidence-based insights for optimizing the risk-benefit balance of ICI therapies in clinical practice.https://www.scienceopen.com/hosted-document?doi=10.15212/AMM-2023-0037
spellingShingle Peipei Ouyang
Weiting Yang
Jianqiao Sun
Ping Chen
Qingyun He
Jiaxin Yan
Wenhao Wang
Yi Wang
Heran Li
Qiuhua Luo
Endocrine toxicity of immune checkpoint inhibitors: a network meta-analysis of the current evidence
Acta Materia Medica
title Endocrine toxicity of immune checkpoint inhibitors: a network meta-analysis of the current evidence
title_full Endocrine toxicity of immune checkpoint inhibitors: a network meta-analysis of the current evidence
title_fullStr Endocrine toxicity of immune checkpoint inhibitors: a network meta-analysis of the current evidence
title_full_unstemmed Endocrine toxicity of immune checkpoint inhibitors: a network meta-analysis of the current evidence
title_short Endocrine toxicity of immune checkpoint inhibitors: a network meta-analysis of the current evidence
title_sort endocrine toxicity of immune checkpoint inhibitors a network meta analysis of the current evidence
url https://www.scienceopen.com/hosted-document?doi=10.15212/AMM-2023-0037
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