Exploring the Use of Monoclonal Antibodies and Antiviral Therapies for Early Treatment of COVID-19 Outpatients in a Real-World Setting: A Nationwide Study from England and Italy.

IF 5.4 2区 医学 Q1 IMMUNOLOGY BioDrugs Pub Date : 2023-09-01 DOI:10.1007/s40259-023-00601-w
Francesco Ciccimarra, Nicoletta Luxi, Chiara Bellitto, Luca L' Abbate, Pasquale De Nardo, Alessia Savoldi, Alison Yeomans, Mariam Molokhia, Evelina Tacconelli, Gianluca Trifirò
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引用次数: 1

Abstract

Background: Real-world data on early treatment of coronavirus disease 2019 (COVID-19) outpatients with newly approved therapies are sparse.

Aim: To explore the pattern of use of monoclonal antibodies (mAbs)/antiviral therapies approved for early COVID-19 treatment in non-hospitalized patients from England and Italy from December 2021 to October 2022.

Methods: Public national dashboards on weekly mAb/antiviral use and/or severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection diagnoses from the Italian Medicines Agency, the Italian National Institute of Health, National Health Service in England and the UK Government were explored. Prevalence of antiviral use in outpatients during the entire study period and every two weeks was calculated, as a whole and by class and compounds. An interrupted time-series (ITS) analysis was carried out to assess the impact of predominant SARS-CoV-2 variants over time on the prevalence of use of mAbs/antivirals in England and Italy.

Results: Overall, 77,469 and 195,604 doses of mAbs/antivirals were respectively administered to a total of 10,630,903 (7.3 per 1000) and 18,168,365 (10.8 per 1000) patients diagnosed with SARS-CoV-2 infection in England and Italy. Prevalence of use every two weeks increased from 0.07% to 3.1% in England and 0.9% to 2.3% in Italy during the study period. Regarding individual compounds, sotrovimab (prevalence of use, 1.6%) and nirmatrelvir/ritonavir (1.6%) in England, and nirmatrelvir/ritonavir (1.7%) and molnupiravir (0.5%) in Italy, reported the highest prevalence during a 2-week period. In the ITS analysis, the transition from Delta to Omicron variant predominance was associated with a significant increase in the use of sotrovimab, molnupiravir, remdesivir and nirmatrelvir/ritonavir in both England and Italy, with a reduction of other marketed mAbs. The extent of the increase was higher in England than in Italy for all these drugs except for nirmatrelvir/ritonavir.

Conclusions: In this dual nationwide study, the prevalence of use of mAbs/antivirals against SARS-CoV-2 for early outpatients' treatment increased slowly up to 2.0-3.0% of all patients diagnosed with SARS-CoV-2 infection in both England and Italy from December 2021 to October 2022. The trend of individual drug use varied in relation to predominant SARS-CoV-2 variants with some differences across countries. In line with scientific societies' guidelines, nirmatrelvir/ritonavir was the most frequently prescribed antiviral in both countries in the most recent period.

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探索在现实世界中使用单克隆抗体和抗病毒疗法早期治疗COVID-19门诊患者:一项来自英国和意大利的全国性研究。
背景:关于2019冠状病毒病(COVID-19)门诊患者使用新批准疗法早期治疗的真实世界数据很少。目的:探讨2021年12月至2022年10月英国和意大利非住院患者早期COVID-19获批单克隆抗体/抗病毒疗法的使用模式。方法:对意大利药品管理局、意大利国家卫生研究所、英格兰国家卫生服务中心和英国政府提供的每周单抗/抗病毒药物使用和/或严重急性呼吸综合征冠状病毒2 (SARS-CoV-2)感染诊断的公共国家仪表板进行研究。在整个研究期间和每两周计算门诊患者抗病毒药物使用的流行率,作为一个整体,按类别和化合物计算。进行了中断时间序列(ITS)分析,以评估随时间变化的主要SARS-CoV-2变体对英格兰和意大利单克隆抗体/抗病毒药物使用流行率的影响。结果:总体而言,在英国和意大利,分别为10,630,903(每1000人中有7.3人)和18,168,365(每1000人中有10.8人)诊断为SARS-CoV-2感染的患者提供了77,469剂和195,604剂单克隆抗体/抗病毒药物。在研究期间,英国每两周使用一次的患病率从0.07%上升到3.1%,意大利从0.9%上升到2.3%。就单个化合物而言,英国的sotrovimab(使用率为1.6%)和nirmatrelvir/ritonavir(使用率为1.6%),意大利的nirmatrelvir/ritonavir(使用率为1.7%)和molnupiravir(使用率为0.5%)在2周内报告的使用率最高。在ITS分析中,从Delta到Omicron变体优势的转变与英国和意大利sotrovimab、molnupiravir、remdesivir和nirmatrelvir/ritonavir的使用显著增加有关,而其他已上市的单抗则减少。除尼马特利韦/利托那韦外,所有这些药物在英国的增长幅度都高于意大利。结论:在这项双重全国性研究中,从2021年12月至2022年10月,在英国和意大利,所有确诊为SARS-CoV-2感染的患者中,早期门诊患者使用抗SARS-CoV-2单克隆抗体/抗病毒药物的患病率缓慢上升至2.0-3.0%。个人药物使用趋势因主要的SARS-CoV-2变体而异,各国之间存在一些差异。根据科学学会的指导方针,nirmatrelvir/ritonavir是这两个国家最近最常用的抗病毒药物。
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来源期刊
BioDrugs
BioDrugs 医学-免疫学
CiteScore
12.60
自引率
2.90%
发文量
50
审稿时长
>12 weeks
期刊介绍: An essential resource for R&D professionals and clinicians with an interest in biologic therapies. BioDrugs covers the development and therapeutic application of biotechnology-based pharmaceuticals and diagnostic products for the treatment of human disease. BioDrugs offers a range of additional enhanced features designed to increase the visibility, readership and educational value of the journal’s content. Each article is accompanied by a Key Points summary, giving a time-efficient overview of the content to a wide readership. Articles may be accompanied by plain language summaries to assist patients, caregivers and others in understanding important medical advances. The journal also provides the option to include various other types of enhanced features including slide sets, videos and animations. All enhanced features are peer reviewed to the same high standard as the article itself. Peer review is conducted using Editorial Manager®, supported by a database of international experts. This database is shared with other Adis journals.
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