REGEN-COV antibody combination in patients with lymphoproliferative malignancies and SARS-CoV-2 infection
- PMID: 35602247
- PMCID: PMC9110987
- DOI: 10.1002/jha2.403
REGEN-COV antibody combination in patients with lymphoproliferative malignancies and SARS-CoV-2 infection
Abstract
Patients with lymphoproliferative diseases are at high risk for SARS-CoV-2-related complications and mortality. The role of casirivimab and imdevimab (REGEN-COV), a neutralizing antibody cocktail, to treat immunocompromised hemato-oncological patients with SARS-CoV-2 disease 2019 (Covid-19) remains unknown. Here, we present our clinical experience on the outcome of 15 hematological patients treated with REGEN-COV for SARS-CoV-2 infection. Most patients failed to respond or achieved low antibody titer after 2-3 doses of BNT162b2 mRNA vaccine. All patients experienced clinical improvement with no mortality within a median follow-up of 70 days. In conclusion, early administration of REGEN-COV to high-risk hematological patients may prevent clinical deterioration and mortality from SARS-CoV-2 infection. The effectiveness of neutralizing antibodies may vary depending on the virus variants and in particular with the omicron variant (B.1.1.529).
Keywords: Covid‐19; REGEN‐COV; SARS‐Cov‐2; lymphoproliferative malignancies.
© 2022 The Authors. eJHaem published by British Society for Haematology and John Wiley & Sons Ltd.
References
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- Coronavirus (COVID‐19) update: FDA authorizes monoclonal antibodies for treatment of COVID‐19. November 21, 2020. https://www.fda.gov/news-events/press-announcements/coronavirus-covid-19...
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