4.7 Article

Pre-exposure prophylaxis with tixagevimab and cilgavimab (Evusheld) for COVID-19 among 1112 severely immunocompromised patients

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CLINICAL MICROBIOLOGY AND INFECTION
卷 28, 期 12, 页码 -

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ELSEVIER SCI LTD
DOI: 10.1016/j.cmi.2022.07.015

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Cilgavimab; COVID-19; Immunocompromised; Monoclonal antibodies; Preexposure prophylaxis; SARS-CoV-2; Tixagevimab

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This study aimed to investigate the incidence and outcomes of COVID-19 among immunocompromised patients receiving tixagevimab/cilgavimab as preexposure prophylaxis. The results showed a low rate of infections and severe illnesses among patients treated with tixagevimab/cilgavimab, suggesting the effectiveness of this preventive strategy for severely immunocompromised patients.
Objective: Immunocompromised patients have an increased risk of a severe form of COVID-19. The clinical efficacy of the tixagevimab/cilgavimab monoclonal antibody combination as pre-exposure prophylaxis against BA.1 and BA.2 SARS-CoV-2 Omicron sublineages is unknown. We aimed to describe the incidence and outcomes of COVID-19 among immunocompromised patients receiving tixagevimab/cilgavimab as preexposure prophylaxis during the Omicron wave in France. Methods: This was an observational multicentre cohort study of immunocompromised patients receiving tixagevimab/cilgavimab as preexposure prophylaxis between December 28, 2021 and March 31, 2022. Patients received tixagevimab/cilgavimab 150/150 mg intramuscularly if they had impaired vaccine response and a high risk of severe form of COVID-19. Results: Tixagevimab/cilgavimab was administered to 1112 immunocompromised patients. After a median (range) follow-up of 63 (49e73) days, COVID-19 was confirmed in 49/1112 (4.4%) >= 5 days after treatment. During the study period, mean weekly incidence rate was 1669 in 100 000 inhabitants in Ile- de-France and 530 in 100 000 among patients who received tixagevimab/cilgavimab prophylaxis. Among infected patients, 43/49 (88%) had a mild-to-moderate form and 6/49 (12%) had a moderate-to-severe form of COVID-19. Patients with moderate-to-severe illnesses were less likely to have received early therapies than patients with mild forms (53.5% vs. 16.7% respectively) and 2/49 (4%) patients died from COVID-19. Discussion: Our study reported a low rate of infections and severe illnesses among immunocompromised patients treated with tixagevimab/cilgavimab. A global preventive strategy including vaccines, preexposure prophylaxis with monoclonal antibodies, and early therapies might be effective to prevent severe forms of COVID-19 among severely immunocompromised patients. Yann Nguyen, Clin Microbiol Infect 2022;28:1654.e1e1654.e4

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