Romain Euvrard, Marie Robert, Sabine Mainbourg, Stéphane Dalle, Jean-Christophe Lega
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These irAE could be conceptually considered as an indicator of the antitumoral immune response, but the association between irAE and prognosis is still a matter of debate.</p>\n </section>\n \n <section>\n \n <h3> Objective</h3>\n \n <p>The purpose of this study was to investigate the association between the overall survival (OS) and the prevalence of irAE in melanoma.</p>\n </section>\n \n <section>\n \n <h3> Methods</h3>\n \n <p>MEDLINE/PubMed, WebofScience, ClinicalTrials, and WHOTrials databases were searched to identify phase 3 randomized controlled trials (RCT) assessing ICI in melanoma and published up to April 2021. A weighted regression was performed to estimate this association according to standard method of surrogacy analysis.</p>\n </section>\n \n <section>\n \n <h3> Results</h3>\n \n <p>A total of 14 RCT including 7646 patients (median age: 59.3 years) with melanoma were included. All types of ICI were represented (ipilimumab, tremelimumab, pembrolizumab, nivolumab, atezolizumab, as well as ipilimumab and nivolumab combination). irAE were frequent but rarely fatal. The combination of ICI caused more irAE than anti-PD1 (or PDL1) and anti-CTLA4 monotherapies. No relationship was found between the occurrence of irAE and OS (beta coefficient 0.078, R<sup>2</sup> 3%, <i>p</i> = 0.52), nor between cutaneous irAE and OS (beta coefficient 0.080, R<sup>2</sup> 6%, <i>p</i> = 0.33).</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Although limited by the heterogeneity of ICI included in the regression and the low number of included RCT, the present study suggests an absence of association between irAE and prognosis in melanoma.</p>\n </section>\n </div>","PeriodicalId":12657,"journal":{"name":"Fundamental & Clinical Pharmacology","volume":null,"pages":null},"PeriodicalIF":2.1000,"publicationDate":"2023-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/fcp.12966","citationCount":"0","resultStr":"{\"title\":\"Association between immune-related adverse events and prognosis in patients treated with immune checkpoint inhibitors in melanoma: A surrogacy analysis\",\"authors\":\"Romain Euvrard, Marie Robert, Sabine Mainbourg, Stéphane Dalle, Jean-Christophe Lega\",\"doi\":\"10.1111/fcp.12966\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background</h3>\\n \\n <p>Immune checkpoint inhibitors (ICI) represent a breakthrough in oncology in terms of prognosis and safety. 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引用次数: 0
摘要
背景:免疫检查点抑制剂(ICI)在肿瘤预后和安全性方面取得了突破性进展。它们现在构成了转移性黑色素瘤治疗的基石。然而,一种新的不良事件被称为免疫相关不良事件(irAE)已经出现。这些irAE可以在概念上被认为是抗肿瘤免疫反应的一个指标,但irAE与预后之间的关系仍然是一个有争议的问题。目的:本研究的目的是探讨黑色素瘤患者总生存期(OS)与irAE患病率之间的关系。方法:检索MEDLINE/PubMed、WebofScience、ClinicalTrials和WHOTrials数据库,以确定评估黑素瘤ICI的3期随机对照试验(RCT),并发表至2021年4月。根据代孕分析的标准方法进行加权回归来估计这种关联。结果:共纳入14项随机对照试验,包括7646例黑色素瘤患者(中位年龄:59.3岁)。代表了所有类型的ICI (ipilimumab, tremelimumab, pembrolizumab, nivolumab, atezolizumab,以及ipilimumab和nivolumab联合)。伊拉克战争频繁发生,但很少致命。ICI联合治疗比抗pd1(或PDL1)和抗ctla4单药治疗引起更多的irAE。irAE的发生与OS无相关性(β系数0.078,R2 3%, p = 0.52),皮肤irAE与OS无相关性(β系数0.080,R2 6%, p = 0.33)。结论:尽管受回归中ICI异质性和纳入的RCT数量较少的限制,本研究提示irAE与黑色素瘤预后之间不存在关联。
Association between immune-related adverse events and prognosis in patients treated with immune checkpoint inhibitors in melanoma: A surrogacy analysis
Background
Immune checkpoint inhibitors (ICI) represent a breakthrough in oncology in terms of prognosis and safety. They now constitute a cornerstone in the management of metastatic melanoma. However, a new kind of adverse event called immune-related adverse events (irAE) has emerged. These irAE could be conceptually considered as an indicator of the antitumoral immune response, but the association between irAE and prognosis is still a matter of debate.
Objective
The purpose of this study was to investigate the association between the overall survival (OS) and the prevalence of irAE in melanoma.
Methods
MEDLINE/PubMed, WebofScience, ClinicalTrials, and WHOTrials databases were searched to identify phase 3 randomized controlled trials (RCT) assessing ICI in melanoma and published up to April 2021. A weighted regression was performed to estimate this association according to standard method of surrogacy analysis.
Results
A total of 14 RCT including 7646 patients (median age: 59.3 years) with melanoma were included. All types of ICI were represented (ipilimumab, tremelimumab, pembrolizumab, nivolumab, atezolizumab, as well as ipilimumab and nivolumab combination). irAE were frequent but rarely fatal. The combination of ICI caused more irAE than anti-PD1 (or PDL1) and anti-CTLA4 monotherapies. No relationship was found between the occurrence of irAE and OS (beta coefficient 0.078, R2 3%, p = 0.52), nor between cutaneous irAE and OS (beta coefficient 0.080, R2 6%, p = 0.33).
Conclusion
Although limited by the heterogeneity of ICI included in the regression and the low number of included RCT, the present study suggests an absence of association between irAE and prognosis in melanoma.
期刊介绍:
Fundamental & Clinical Pharmacology publishes reports describing important and novel developments in fundamental as well as clinical research relevant to drug therapy. Original articles, short communications and reviews are published on all aspects of experimental and clinical pharmacology including:
Antimicrobial, Antiviral Agents
Autonomic Pharmacology
Cardiovascular Pharmacology
Cellular Pharmacology
Clinical Trials
Endocrinopharmacology
Gene Therapy
Inflammation, Immunopharmacology
Lipids, Atherosclerosis
Liver and G-I Tract Pharmacology
Metabolism, Pharmacokinetics
Neuropharmacology
Neuropsychopharmacology
Oncopharmacology
Pediatric Pharmacology Development
Pharmacoeconomics
Pharmacoepidemiology
Pharmacogenetics, Pharmacogenomics
Pharmacovigilance
Pulmonary Pharmacology
Receptors, Signal Transduction
Renal Pharmacology
Thrombosis and Hemostasis
Toxicopharmacology
Clinical research, including clinical studies and clinical trials, may cover disciplines such as pharmacokinetics, pharmacodynamics, pharmacovigilance, pharmacoepidemiology, pharmacogenomics and pharmacoeconomics. Basic research articles from fields such as physiology and molecular biology which contribute to an understanding of drug therapy are also welcomed.