Efficacy and safety of biological treatment for inflammatory bowel disease in elderly patients: Results from a GETECCU cohort

Cristina Suárez Ferrer , Francisco Mesonero Gismero , Berta Caballol , Maria Pilar Ballester , Iria Bastón Rey , Andrés Castaño García , Jose Miranda Bautista , Rosa Saiz Chumillas , Jose Manuel Benitez , Laura Sanchez-Delgado , Alicia López-García , Cristina Rubin de Celix , Inmaculada Alonso Abreu , Luigi Melcarne , Rocío Plaza Santos , Miquel Marques-Camí , Antonio Caballero Mateos , César Gómez Díez , Margalida Calafat , Horacio Alonso Galan , Manuel Barreiro-De Acosta
{"title":"Efficacy and safety of biological treatment for inflammatory bowel disease in elderly patients: Results from a GETECCU cohort","authors":"Cristina Suárez Ferrer ,&nbsp;Francisco Mesonero Gismero ,&nbsp;Berta Caballol ,&nbsp;Maria Pilar Ballester ,&nbsp;Iria Bastón Rey ,&nbsp;Andrés Castaño García ,&nbsp;Jose Miranda Bautista ,&nbsp;Rosa Saiz Chumillas ,&nbsp;Jose Manuel Benitez ,&nbsp;Laura Sanchez-Delgado ,&nbsp;Alicia López-García ,&nbsp;Cristina Rubin de Celix ,&nbsp;Inmaculada Alonso Abreu ,&nbsp;Luigi Melcarne ,&nbsp;Rocío Plaza Santos ,&nbsp;Miquel Marques-Camí ,&nbsp;Antonio Caballero Mateos ,&nbsp;César Gómez Díez ,&nbsp;Margalida Calafat ,&nbsp;Horacio Alonso Galan ,&nbsp;Manuel Barreiro-De Acosta","doi":"10.1016/j.gastre.2024.502197","DOIUrl":null,"url":null,"abstract":"<div><h3>Introduction</h3><div>Biological therapies used for the treatment of inflammatory bowel disease (IBD) have shown to be effective and safe, although these results were obtained from studies involving mostly a young population, who are generally included in clinical trials. The aim of our study was to determine the efficacy and safety of the different biological treatments in the elderly population.</div></div><div><h3>Methods</h3><div>Multicenter study was carried out in the GETECCU group. Patients diagnosed with IBD and aged over 65 years at the time of initiating biological therapy (infliximab, adalimumab, golimumab, ustekinumab or vedolizumab) were retrospectively included.</div><div>Among the patients included, clinical response was assessed after drug induction (12 weeks of treatment) and at 52 weeks. Patients’ colonoscopy data in week 52 were assessment, where available. Regarding complications, development of oncological events during follow-up and infectious processes occurring during biological treatment were collected (excluding bowel infection by cytomegalovirus).</div></div><div><h3>Results</h3><div>A total of 1090 patients were included. After induction, at approximately 12–14 weeks of treatment, 419 patients (39.6%) were in clinical remission, 502 patients (47.4%) had responded without remission and 137 patients (12.9%) had no response.</div><div>At 52 weeks of treatment 442 patients (57.1%) had achieved clinical remission, 249 patients had responded without remission (32.2%) and 53 patients had no response to the treatment (6.8%). Before 52 weeks, 129 patients (14.8%) had discontinued treatment due to inefficacy, this being significantly higher (<em>p</em> <!-->&lt;<!--> <!-->0.0001) for Golimumab – 9 patients (37.5%) – compared to the other biological treatments analyzed.</div><div>With respect to tumor development, an oncological event was observed in 74 patients (6.9%): 30 patients (8%) on infliximab, 23 (7.14%) on adalimumab, 3 (11.1%) on golimumab, 10 (6.4%) on ustekinumab, and 8 (3.8%) on vedolizumab. The incidence was significantly lower (<em>p</em> <!-->=<!--> <!-->0.04) for the vedolizumab group compared to other treatments.</div><div>As regards infections, these occurred in 160 patients during treatment (14.9%), with no differences between the different biologicals used (<em>p</em> <!-->=<!--> <!-->0.61): 61 patients (19.4%) on infliximab, 39 (12.5%) on adalimumab, 5 (17.8%) on golimumab, 22 (14.1%) on ustekinumab, and 34 (16.5%) on vedolizumab.</div></div><div><h3>Conclusions</h3><div>Biological drug therapies have response rates in elderly patients similar to those described in the general population, Golimumab was the drug that was discontinued most frequently due to inefficacy.</div><div>In our experience, tumor development was more frequent in patients who used anti-TNF therapies compared to other targets, although its incidence was generally low and that this is in line with younger patients based on previous literature.</div></div>","PeriodicalId":100569,"journal":{"name":"Gastroenterología y Hepatología (English Edition)","volume":"47 10","pages":"Article 502197"},"PeriodicalIF":0.0000,"publicationDate":"2024-11-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Gastroenterología y Hepatología (English Edition)","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2444382424002487","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction

Biological therapies used for the treatment of inflammatory bowel disease (IBD) have shown to be effective and safe, although these results were obtained from studies involving mostly a young population, who are generally included in clinical trials. The aim of our study was to determine the efficacy and safety of the different biological treatments in the elderly population.

Methods

Multicenter study was carried out in the GETECCU group. Patients diagnosed with IBD and aged over 65 years at the time of initiating biological therapy (infliximab, adalimumab, golimumab, ustekinumab or vedolizumab) were retrospectively included.
Among the patients included, clinical response was assessed after drug induction (12 weeks of treatment) and at 52 weeks. Patients’ colonoscopy data in week 52 were assessment, where available. Regarding complications, development of oncological events during follow-up and infectious processes occurring during biological treatment were collected (excluding bowel infection by cytomegalovirus).

Results

A total of 1090 patients were included. After induction, at approximately 12–14 weeks of treatment, 419 patients (39.6%) were in clinical remission, 502 patients (47.4%) had responded without remission and 137 patients (12.9%) had no response.
At 52 weeks of treatment 442 patients (57.1%) had achieved clinical remission, 249 patients had responded without remission (32.2%) and 53 patients had no response to the treatment (6.8%). Before 52 weeks, 129 patients (14.8%) had discontinued treatment due to inefficacy, this being significantly higher (p < 0.0001) for Golimumab – 9 patients (37.5%) – compared to the other biological treatments analyzed.
With respect to tumor development, an oncological event was observed in 74 patients (6.9%): 30 patients (8%) on infliximab, 23 (7.14%) on adalimumab, 3 (11.1%) on golimumab, 10 (6.4%) on ustekinumab, and 8 (3.8%) on vedolizumab. The incidence was significantly lower (p = 0.04) for the vedolizumab group compared to other treatments.
As regards infections, these occurred in 160 patients during treatment (14.9%), with no differences between the different biologicals used (p = 0.61): 61 patients (19.4%) on infliximab, 39 (12.5%) on adalimumab, 5 (17.8%) on golimumab, 22 (14.1%) on ustekinumab, and 34 (16.5%) on vedolizumab.

Conclusions

Biological drug therapies have response rates in elderly patients similar to those described in the general population, Golimumab was the drug that was discontinued most frequently due to inefficacy.
In our experience, tumor development was more frequent in patients who used anti-TNF therapies compared to other targets, although its incidence was generally low and that this is in line with younger patients based on previous literature.
老年炎症性肠病生物治疗的有效性和安全性:来自 GETECCU 队列的结果
导言用于治疗炎症性肠病(IBD)的生物疗法已被证明是有效和安全的,尽管这些结果都是在主要涉及年轻人群的研究中获得的,而年轻人群通常被纳入临床试验中。我们的研究旨在确定不同生物疗法在老年人群中的疗效和安全性。回顾性纳入了在开始接受生物疗法(英夫利昔单抗、阿达木单抗、戈利木单抗、乌斯特库单抗或维多珠单抗)时确诊为 IBD 且年龄超过 65 岁的患者。如果有患者第52周的结肠镜检查数据,则对其进行评估。在并发症方面,收集了随访期间发生的肿瘤事件和生物治疗期间发生的感染过程(不包括巨细胞病毒引起的肠道感染)。诱导治疗后,在大约 12-14 周的治疗中,419 名患者(39.6%)获得临床缓解,502 名患者(47.4%)有反应但未缓解,137 名患者(12.9%)无反应。在52周之前,有129名患者(14.8%)因疗效不佳而中断治疗,与其他生物疗法相比,戈利木单抗的中断率明显更高(p < 0.0001),有9名患者(37.5%)中断了治疗:74名患者(6.9%)中观察到肿瘤事件:使用英夫利西单抗的患者有30名(8%),使用阿达木单抗的患者有23名(7.14%),使用戈利木单抗的患者有3名(11.1%),使用乌司他单抗的患者有10名(6.4%),使用维多单抗的患者有8名(3.8%)。在感染方面,160 名患者(14.9%)在治疗期间发生感染,不同生物制剂之间没有差异(p = 0.61):61名患者(19.4%)使用英夫利昔单抗,39名患者(12.5%)使用阿达木单抗,5名患者(17.8%)使用戈利木单抗,22名患者(14.1%)使用乌司他单抗,34名患者(16.5%)使用维多珠单抗。根据我们的经验,与其他靶点相比,使用抗肿瘤坏死因子疗法的患者更容易出现肿瘤发生,尽管其发生率普遍较低,而且根据以往的文献,这与年轻患者的情况一致。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
自引率
0.00%
发文量
0
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信