Use of casirivimab and imdevimab to prevent progression to severe COVID-19
Mir Shahnawaz, Tajamul Hussain, Naeem Firdous, Mohammad Yousoof, Hafsa M Gundroo, Yashpal Sharma, Dr Naveed Nazir Shah
Journal of Integrative Medicine and Public Health, doi:10.4103/jimph.jimph_23_24
BACKGROUND: Advanced age and the presence of comorbid illnesses increase the risk of disease progression and death in patients infected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV2). Several neutralizing antibodies against SARS-CoV2 have been developed for the management of mild to moderate coronavirus disease 2019 (COVID-19) at risk of disease progression. This study aimed to evaluate the effect of a combination of casirivimab and imdevimab (REGN-COV2) on disease progression/hospitalization in mild-to-moderate COVID-19.
MATERIALS AND METHODS: It is a prospective interventional study, patients with mild-to-moderate COVID-19 were included in the study. The illnesses with risk factors for disease progression were divided into two groups, one who received a combination of casirivimab and imdevimab (REGN-COV2) cocktail and the other who received usual care. The primary outcome of the study was a comparison of disease progression or hospitalization on day 14 after treatment. Secondary outcomes included viral clearance, mortality, and effect on proinflammatory markers.
RESULTS: A total of 169 patients with mild-to-moderate COVID-19 illness with risk factors for disease progression were included in the study. About 85 patients (50.3%) as cases received REGN-COV2 whereas 84 (49.7%) as control received usual care only. Hospitalization or progression of disease was significantly lower in patients who received REGN-COV2 than in the usual care only [14.12% vs. 27.38%; relative risk (RR) = 0.51, 95% confidence interval (CI) = 0.27-0.95, P = 0.03]. Time taken for viral clearance was again lower in intervention group [median = 9 days, interquartile range (IQR) = [8-11] vs. median =13 days, IQR [10-14], P < 0.001] as was serum levels of C-reactive protein (CRP) and interleukin (IL)-6 significantly reduced in patients who received REGN-COV2 [CRP, median = 11.5 (5.75-34) to 4 (2-9), P = 0.001 and IL-6, median 10 (4-23.5) to 3 (2-7), P = 0.001]. Three patients in the usual care group died due to worsening respiratory failure compared with none in the REGN-COV2 group. Only minor adverse events were noticed in 8.2% (n = 7) patients in the REGN-COV2 group with no life-threatening events observed.
CONCLUSION: In mild-to-moderate COVID-19 patients at high risk of disease progression REGN-COV2 treatment significantly reduced progression of disease and hospitalization without significant adverse events.
Financial support and sponsorship Nil.
Conflicts of interest There are no conflicts of interest.
References
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Westblade, Brar, Pinheiro, Paidoussis, Rajan et al., SARS-CoV-2 Viral load predicts mortality in patients with and without cancer who are hospitalized with COVID-19, Cancer Cell
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"abstract": "<jats:title>Abstract</jats:title>\n <jats:sec>\n <jats:title>BACKGROUND:</jats:title>\n <jats:p>Advanced age and the presence of comorbid illnesses increase the risk of disease progression and death in patients infected by severe acute respiratory syndrome coronavirus 2 (SARS-CoV2). Several neutralizing antibodies against SARS-CoV2 have been developed for the management of mild to moderate coronavirus disease 2019 (COVID-19) at risk of disease progression. This study aimed to evaluate the effect of a combination of casirivimab and imdevimab (REGN-COV2) on disease progression/hospitalization in mild-to-moderate COVID-19.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>MATERIALS AND METHODS:</jats:title>\n <jats:p>It is a prospective interventional study, patients with mild-to-moderate COVID-19 were included in the study. The illnesses with risk factors for disease progression were divided into two groups, one who received a combination of casirivimab and imdevimab (REGN-COV2) cocktail and the other who received usual care. The primary outcome of the study was a comparison of disease progression or hospitalization on day 14 after treatment. Secondary outcomes included viral clearance, mortality, and effect on proinflammatory markers.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>RESULTS:</jats:title>\n <jats:p>A total of 169 patients with mild-to-moderate COVID-19 illness with risk factors for disease progression were included in the study. About 85 patients (50.3%) as cases received REGN-COV2 whereas 84 (49.7%) as control received usual care only. Hospitalization or progression of disease was significantly lower in patients who received REGN-COV2 than in the usual care only [14.12% vs. 27.38%; relative risk (RR) = 0.51, 95% confidence interval (CI) = 0.27−0.95, <jats:italic toggle=\"yes\">P</jats:italic> = 0.03]. Time taken for viral clearance was again lower in intervention group [median = 9 days, interquartile range (IQR) = [8–11] vs. median =13 days, IQR [10–14], <jats:italic toggle=\"yes\">P</jats:italic> < 0.001] as was serum levels of C-reactive protein (CRP) and interleukin (IL)-6 significantly reduced in patients who received REGN-COV2 [CRP, median = 11.5 (5.75–34) to 4 (2–9), <jats:italic toggle=\"yes\">P</jats:italic> = 0.001 and IL-6, median 10 (4–23.5) to 3 (2–7), <jats:italic toggle=\"yes\">P</jats:italic> = 0.001]. Three patients in the usual care group died due to worsening respiratory failure compared with none in the REGN-COV2 group. Only minor adverse events were noticed in 8.2% (<jats:italic toggle=\"yes\">n</jats:italic> = 7) patients in the REGN-COV2 group with no life-threatening events observed.</jats:p>\n </jats:sec>\n <jats:sec>\n <jats:title>CONCLUSION:</jats:title>\n <jats:p>In mild-to-moderate COVID-19 patients at high risk of disease progression REGN-COV2 treatment significantly reduced progression of disease and hospitalization without significant adverse events.</jats:p>\n </jats:sec>",
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