Cargando…
535. Comparison of Outcomes in Patients Positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection After Monoclonal Antibody Therapy (MAT) with Bamlamivimab or Casirivimab-Imdevimab
BACKGROUND: Limited options currently exist for treatment of patients diagnosed with symptomatic coronavirus 2019 (COVID-19). Monoclonal antibody therapy (MAT) has been investigated as a therapeutic option for symptomatic COVID-19 patients in the outpatient setting at high-risk for progression to se...
Autores principales: | , , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Oxford University Press
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8690747/ http://dx.doi.org/10.1093/ofid/ofab466.734 |
_version_ | 1784618682192756736 |
---|---|
author | Nichols, Courtney Lustberg, Mark Sobhanie, Mohammad Mahdee Lehman, Joy Reed, Erica E Kman, Nicholas E Conroy, Mark Dick, Michael Allen, James N Parsons, Jonathan Malvestutto, Carlos |
author_facet | Nichols, Courtney Lustberg, Mark Sobhanie, Mohammad Mahdee Lehman, Joy Reed, Erica E Kman, Nicholas E Conroy, Mark Dick, Michael Allen, James N Parsons, Jonathan Malvestutto, Carlos |
author_sort | Nichols, Courtney |
collection | PubMed |
description | BACKGROUND: Limited options currently exist for treatment of patients diagnosed with symptomatic coronavirus 2019 (COVID-19). Monoclonal antibody therapy (MAT) has been investigated as a therapeutic option for symptomatic COVID-19 patients in the outpatient setting at high-risk for progression to severe disease based on emergency use authorization (EUA) criteria. No published studies have compared outcomes for patients treated with different MAT for COVID-19. METHODS: This was a single-center, retrospective cohort study at The Ohio State University Wexner Medical Center to compare COVID-19-related emergency room (ER) visits, admissions, and mortality at 30 days after MAT infusion for adult patients with symptomatic SARS-CoV-2 between November 16, 2020 and February 2, 2021 who received bamlanivimab versus those who received casirivimab-imdevimab. Statistical analysis used logistic regression analysis to determine the odds ratio (OR) to evaluate the relationship between patient characteristics, MAT, and outcomes. RESULTS: The cohort included 943 patients with SARS-CoV-2 who received MAT, including 658 patients who received bamlanivimab and 285 who received casirivimab-imdevimab. Outcome results between patients who received bamlanivimab and casirivimab-imdevimab showed no statistically significant difference seen in the number of COVID-19 related ER visits (3.2% vs 3.5%, p = 0.80), hospital admissions (4.6% vs 2.8%, p = 0.21), or mortality (0.5% vs 0.7%, p = 0.63). Multivariate analysis showed no statistically significant difference in outcomes between the groups when accounting for potential confounders. As reflected in the Table, chronic lymphocytic leukemia (CLL), gender, and asthma were associated with increased COVID-19 related ER visit within 30 days of infusion and age, chronic obstructive pulmonary disease, CLL, and lupus were associated with increased risk for COVID-19 related admission within 30 days of infusion. Age and obesity with body mass index greater than 35 mg/kg(2) were associated with increased risk for COVID-19 related mortality at 30 days. [Image: see text] CONCLUSION: COVID-19 related outcomes were similar when comparing patients with COVID-19 treated with bamlanivimab versus those treated with casirivimab-imdevimab. DISCLOSURES: Mohammad Mahdee Sobhanie, M.D., Regeneron (Scientific Research Study Investigator)Regeneron (Scientific Research Study Investigator, Was a sub-investigator for Regeneron 2066 and 2069) Carlos Malvestutto, M.D., Lilly (Scientific Research Study Investigator)Regeneron Inc. (Scientific Research Study Investigator)ViiV Healthcare (Advisor or Review Panel member) |
format | Online Article Text |
id | pubmed-8690747 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Oxford University Press |
record_format | MEDLINE/PubMed |
spelling | pubmed-86907472022-01-05 535. Comparison of Outcomes in Patients Positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection After Monoclonal Antibody Therapy (MAT) with Bamlamivimab or Casirivimab-Imdevimab Nichols, Courtney Lustberg, Mark Sobhanie, Mohammad Mahdee Lehman, Joy Reed, Erica E Kman, Nicholas E Conroy, Mark Dick, Michael Allen, James N Parsons, Jonathan Malvestutto, Carlos Open Forum Infect Dis Poster Abstracts BACKGROUND: Limited options currently exist for treatment of patients diagnosed with symptomatic coronavirus 2019 (COVID-19). Monoclonal antibody therapy (MAT) has been investigated as a therapeutic option for symptomatic COVID-19 patients in the outpatient setting at high-risk for progression to severe disease based on emergency use authorization (EUA) criteria. No published studies have compared outcomes for patients treated with different MAT for COVID-19. METHODS: This was a single-center, retrospective cohort study at The Ohio State University Wexner Medical Center to compare COVID-19-related emergency room (ER) visits, admissions, and mortality at 30 days after MAT infusion for adult patients with symptomatic SARS-CoV-2 between November 16, 2020 and February 2, 2021 who received bamlanivimab versus those who received casirivimab-imdevimab. Statistical analysis used logistic regression analysis to determine the odds ratio (OR) to evaluate the relationship between patient characteristics, MAT, and outcomes. RESULTS: The cohort included 943 patients with SARS-CoV-2 who received MAT, including 658 patients who received bamlanivimab and 285 who received casirivimab-imdevimab. Outcome results between patients who received bamlanivimab and casirivimab-imdevimab showed no statistically significant difference seen in the number of COVID-19 related ER visits (3.2% vs 3.5%, p = 0.80), hospital admissions (4.6% vs 2.8%, p = 0.21), or mortality (0.5% vs 0.7%, p = 0.63). Multivariate analysis showed no statistically significant difference in outcomes between the groups when accounting for potential confounders. As reflected in the Table, chronic lymphocytic leukemia (CLL), gender, and asthma were associated with increased COVID-19 related ER visit within 30 days of infusion and age, chronic obstructive pulmonary disease, CLL, and lupus were associated with increased risk for COVID-19 related admission within 30 days of infusion. Age and obesity with body mass index greater than 35 mg/kg(2) were associated with increased risk for COVID-19 related mortality at 30 days. [Image: see text] CONCLUSION: COVID-19 related outcomes were similar when comparing patients with COVID-19 treated with bamlanivimab versus those treated with casirivimab-imdevimab. DISCLOSURES: Mohammad Mahdee Sobhanie, M.D., Regeneron (Scientific Research Study Investigator)Regeneron (Scientific Research Study Investigator, Was a sub-investigator for Regeneron 2066 and 2069) Carlos Malvestutto, M.D., Lilly (Scientific Research Study Investigator)Regeneron Inc. (Scientific Research Study Investigator)ViiV Healthcare (Advisor or Review Panel member) Oxford University Press 2021-12-04 /pmc/articles/PMC8690747/ http://dx.doi.org/10.1093/ofid/ofab466.734 Text en © The Author(s) 2021. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Poster Abstracts Nichols, Courtney Lustberg, Mark Sobhanie, Mohammad Mahdee Lehman, Joy Reed, Erica E Kman, Nicholas E Conroy, Mark Dick, Michael Allen, James N Parsons, Jonathan Malvestutto, Carlos 535. Comparison of Outcomes in Patients Positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection After Monoclonal Antibody Therapy (MAT) with Bamlamivimab or Casirivimab-Imdevimab |
title | 535. Comparison of Outcomes in Patients Positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection After Monoclonal Antibody Therapy (MAT) with Bamlamivimab or Casirivimab-Imdevimab |
title_full | 535. Comparison of Outcomes in Patients Positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection After Monoclonal Antibody Therapy (MAT) with Bamlamivimab or Casirivimab-Imdevimab |
title_fullStr | 535. Comparison of Outcomes in Patients Positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection After Monoclonal Antibody Therapy (MAT) with Bamlamivimab or Casirivimab-Imdevimab |
title_full_unstemmed | 535. Comparison of Outcomes in Patients Positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection After Monoclonal Antibody Therapy (MAT) with Bamlamivimab or Casirivimab-Imdevimab |
title_short | 535. Comparison of Outcomes in Patients Positive for Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Infection After Monoclonal Antibody Therapy (MAT) with Bamlamivimab or Casirivimab-Imdevimab |
title_sort | 535. comparison of outcomes in patients positive for severe acute respiratory syndrome coronavirus 2 (sars-cov-2) infection after monoclonal antibody therapy (mat) with bamlamivimab or casirivimab-imdevimab |
topic | Poster Abstracts |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8690747/ http://dx.doi.org/10.1093/ofid/ofab466.734 |
work_keys_str_mv | AT nicholscourtney 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT lustbergmark 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT sobhaniemohammadmahdee 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT lehmanjoy 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT reedericae 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT kmannicholase 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT conroymark 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT dickmichael 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT allenjamesn 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT parsonsjonathan 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab AT malvestuttocarlos 535comparisonofoutcomesinpatientspositiveforsevereacuterespiratorysyndromecoronavirus2sarscov2infectionaftermonoclonalantibodytherapymatwithbamlamivimaborcasirivimabimdevimab |