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针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的单克隆抗体预防多中心大型队列中2019冠状病毒病(COVID-19)病情恶化的研究

Monoclonal antibodies against SARS-CoV-2 to prevent COVID-19 worsening in a large multicenter cohort.

作者信息

Soria Alessandro, Graziano Francesca, Ghilardi Giulia, Lapadula Giuseppe, Gasperina Daniela Dalla, Benatti Simone Vasilij, Quiros-Roldan Eugenia, Milesi Maurizio, Bai Francesca, Merli Marco, Minisci Davide, Franzetti Marco, Asperges Erika, Chiabrando Filippo, Pocaterra Daria, Pandolfo Alessandro, Zanini Fabio, Lombardi Domenico, Cappelletti Anna, Rugova Alban, Borghesi Maria Lucia, Squillace Nicola, Pusterla Luigi, Piconi Stefania, Morelli Paola, Querini Patrizia Rovere, Bruno Raffaele, Rusconi Stefano, Casari Salvatore, Bandera Alessandra, Franzetti Fabio, Travi Giovanna, D'Arminio Monforte Antonella, Marchetti Giulia, Pan Angelo, Castelli Francesco, Rizzi Marco, Dentali Francesco, Mallardo Maria, Rossi Emanuela, Valsecchi Maria Grazia, Galimberti Stefania, Bonfanti Paolo

机构信息

Clinic of Infectious Diseases, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

Biostatistics and Clinical Epidemiology, Fondazione IRCCS San Gerardo dei Tintori, Monza, Italy.

出版信息

Heliyon. 2024 Aug 13;10(16):e36102. doi: 10.1016/j.heliyon.2024.e36102. eCollection 2024 Aug 30.

Abstract

OBJECTIVE

Monoclonal antibodies (mAbs) against Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) reduced Coronavirus Disease 2019 (COVID-19) hospitalizations in people at risk of clinical worsening. Real-world descriptions are limited.

METHODS

CONDIVIDIAMO, a two-year multicenter observational study, consecutively enrolled SARS-CoV-2 outpatients with ≥1 risk factor for COVID-19 progression receiving mAbs. Demographic data, underlying medical condition, type of mAbs combination received, duration of symptoms before mAbs administration, COVID-19 vaccination history, were collected upon enrolment and centrally recorded. Data on outcomes (hospitalizations, reasons of hospitalization, deaths) were prospectively collected. The primary endpoint was the rate of hospitalization or death in a 28-day follow-up, whichever occurred first; subjects were censored at the day of last follow-up or up to 28 days. The Kaplan-Meier method was used to estimate the incidence rate curve in time. The Cox regression model was used to assess potential risk factors for unfavorable outcome. Results were shown as hazard ratio (HR) along with the corresponding 95 % Confidence Interval (95%CI).

RESULTS

Among 1534 subjects (median [interquartile range, IQR] age 66.5 [52.4-74.9] years, 693 [45.2 %] women), 632 (41.2 %) received bamlanivimab ± etesevimab, 209 (13.6 %) casirivimab/imdevimab, 586 (38.2 %) sotrovimab, 107 (7.0 %) tixagevimab/cilgavimab. After 28-day follow-up, 87/1534 (5.6 %, 95%CI: 4.4%-6.8 %) met the primary outcome (85 hospitalizations, 2 deaths). Hospitalizations for COVID-19 (52, 3.4 %) occurred earlier than for other reasons (33, 2.1 %), after a median (IQR) of 3.5 (1-7) 8 (3-15) days (p = 0.006) from mAbs administration.In a multivariable Cox regression model, factors independently associated with increased hospitalization risk were age (hazard ratio [HR] 1.02, 95%CI 1.00-1.03, p = 0.021), immunodeficiency (HR 1.78, 95%CI 1.11-2.85, p = 0.017), pre-Omicron calendar period (HR 1.66, 95%CI 1.02-2.69, p = 0.041).

CONCLUSIONS

MAbs real-world data over a 2-year changing pandemic landscape showed the feasibility of the intervention, although the hospitalization rate was not negligible. Immunosuppressed subjects remain more at risk of clinical worsening.

摘要

目的

针对严重急性呼吸综合征冠状病毒2(SARS-CoV-2)的单克隆抗体(mAbs)可降低有临床病情恶化风险人群的2019冠状病毒病(COVID-19)住院率。真实世界中的相关描述有限。

方法

CONDIVIDIAMO是一项为期两年的多中心观察性研究,连续纳入有≥1个COVID-19病情进展风险因素且接受mAbs治疗的SARS-CoV-2门诊患者。在入组时收集人口统计学数据、基础疾病状况、接受的mAbs组合类型、mAbs给药前症状持续时间、COVID-19疫苗接种史,并进行集中记录。前瞻性收集结局(住院、住院原因、死亡)数据。主要终点是28天随访期内的住院率或死亡率,以先发生者为准;在最后一次随访日或直至28天时对受试者进行截尾。采用Kaplan-Meier方法估计随时间变化的发病率曲线。使用Cox回归模型评估不良结局的潜在风险因素。结果以风险比(HR)及相应的95%置信区间(95%CI)表示。

结果

在1534名受试者中(年龄中位数[四分位间距,IQR]为66.5[52.4 - 74.9]岁;693名[45.2%]为女性),632名(41.2%)接受巴瑞替尼单抗±依特司韦单抗,209名(13.6%)接受卡西瑞单抗/依美司韦单抗,586名(38.2%)接受索托维单抗,107名(7.0%)接受替沙格韦单抗/西加韦单抗。28天随访后,87/1534名(5.6%,95%CI:4.4% - 6.8%)达到主要结局(85例住院,2例死亡)。COVID-19相关住院(52例,3.4%)比其他原因导致的住院(33例,2.1%)更早出现,分别在mAbs给药后的中位数(IQR)3.5(1 - 7)天和8(3 - 15)天(p = 0.006)。在多变量Cox回归模型中,与住院风险增加独立相关的因素为年龄(风险比[HR]1.02,95%CI 1.00 - 1.03,p = 0.021)、免疫缺陷(HR 1.78,95%CI 1.11 - 2.85,p = 0.017)、奥密克戎变异株出现之前的时间段(HR 1.66,95%CI 1.02 - 2.69,p = 0.041)。

结论

在两年不断变化的疫情形势下,mAbs的真实世界数据显示了该干预措施的可行性,尽管住院率仍不可忽视。免疫抑制受试者临床病情恶化的风险仍然更高。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ff3d/11378919/0ea8a02dba11/gr1.jpg

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