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生物疗法在老年炎症性肠病中的安全性:一项系统评价和荟萃分析。

Safety of Biological Therapies in Elderly Inflammatory Bowel Diseases: A Systematic Review and Meta-Analysis.

作者信息

Hahn Gustavo Drügg, Golovics Petra Anna, Wetwittayakhlang Panu, Santa Maria Dirlene Melo, Britto Usiara, Wild Gary Edward, Afif Waqqas, Bitton Alain, Bessissow Talat, Lakatos Peter Laszlo

机构信息

Division of Gastroenterology, McGill University Health Centre, Montreal, QC H3G 1A4, Canada.

School of Medicine, Graduate Course Sciences in Gastroenterology and Hepatology, Universidade Federal do Rio Grande do Sul, Porto Alegre 90035-002, Brazil.

出版信息

J Clin Med. 2022 Jul 29;11(15):4422. doi: 10.3390/jcm11154422.

Abstract

Newer biologics appeared safer in landmark clinical trials, but their safety is understudied in vulnerable populations. The aim of the present study was to perform a systematic review and meta-analysis to assess the safety of available biologicals in the elderly IBD population. We systematically searched PubMed/Medline and conference proceedings between 1 April 1969 and 1 June 2021 to identify eligible studies that examined the safety of biologics in elderly patients with IBD. Of the 2885 articles and 12 congress abstracts identified, 12 peer reviewed papers and 3 abstracts were included after independent evaluation by two reviewers. The identified studies collected safety data on anti-TNF, vedolizumab (VDZ) and ustekinumab (UST). Rates of AE and infections were not different among the biologics (AE mean rate: 11.3 (CI 95% 9.9-12.7)/100 pts-years; = 0.11, infection mean rate: 9.5 (CI 95% 8.4-10.6)/100 pts-years; = 0.56) in elderly IBD patients on anti-TNF, VDZ or UST. Infusion/injection reaction rates were more common on anti-TNFs (mean rate: 2.51 (CI 95% 1.7-3.4/100 pts-years; = 0.02). and malignancy rates were higher on VDZ/UST (mean rate: 2.14 (CI 95% 1.6-2.8)/100 pts-years; = 0.01). Rates of AEs and infections were not different among biologicals. Infusion/injection reactions were more common on anti-TNFs. Current data are insufficient to suggest the sequencing of biologicals in elderly patients based on safety.

摘要

在具有里程碑意义的临床试验中,新型生物制剂似乎更安全,但在弱势群体中对其安全性的研究不足。本研究的目的是进行系统评价和荟萃分析,以评估现有生物制剂在老年炎症性肠病(IBD)患者中的安全性。我们系统检索了1969年4月1日至2021年6月1日期间的PubMed/Medline和会议论文集,以确定研究生物制剂在老年IBD患者中安全性的合格研究。在识别出的2885篇文章和12篇会议摘要中,经过两名审稿人的独立评估,纳入了12篇同行评审论文和3篇摘要。所识别的研究收集了抗TNF、维多珠单抗(VDZ)和乌司奴单抗(UST)的安全性数据。在接受抗TNF、VDZ或UST治疗的老年IBD患者中,生物制剂之间的不良事件(AE)和感染发生率没有差异(AE平均发生率:11.3(95%CI 9.9-12.7)/100患者-年;P = 0.11,感染平均发生率:9.5(95%CI 8.4-10.6)/100患者-年;P = 0.56)。抗TNF药物的输注/注射反应发生率更常见(平均发生率:2.51(95%CI 1.7-3.4)/100患者-年;P = 0.02),VDZ/UST的恶性肿瘤发生率更高(平均发生率:2.14(95%CI 1.6-2.8)/100患者-年;P = 0.01)。生物制剂之间的AE和感染发生率没有差异。输注/注射反应在抗TNF药物中更常见。目前的数据不足以根据安全性建议老年患者使用生物制剂的顺序。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c54d/9369299/51cfff10f8a5/jcm-11-04422-g001.jpg

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