Experience with sotrovimab treatment of SARS-CoV-2-infected patients in Denmark

Research output: Contribution to journalJournal articleResearchpeer-review

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Experience with sotrovimab treatment of SARS-CoV-2-infected patients in Denmark. / Rasmussen, Line Dahlerup; Lebech, Anne Mette; Øvrehus, Anne; Poulsen, Birgitte Klindt; Christensen, Hanne Rolighed; Nielsen, Henrik; Johansen, Isik Somuncu; Omland, Lars Haukali; Wiese, Lothar; Helleberg, Marie; Storgaard, Merete; Dalager-Pedersen, Michael; Rasmussen, Thomas A.; Benfield, Thomas; Petersen, Tonny Studsgaard; Andersen, Åse Bengård; Gram, Mie Agermose; Stegger, Marc; Edslev, Sofie Marie; Obel, Niels.

In: British Journal of Clinical Pharmacology, Vol. 89, No. 6, 2023, p. 1820-1833.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Rasmussen, LD, Lebech, AM, Øvrehus, A, Poulsen, BK, Christensen, HR, Nielsen, H, Johansen, IS, Omland, LH, Wiese, L, Helleberg, M, Storgaard, M, Dalager-Pedersen, M, Rasmussen, TA, Benfield, T, Petersen, TS, Andersen, ÅB, Gram, MA, Stegger, M, Edslev, SM & Obel, N 2023, 'Experience with sotrovimab treatment of SARS-CoV-2-infected patients in Denmark', British Journal of Clinical Pharmacology, vol. 89, no. 6, pp. 1820-1833. https://doi.org/10.1111/bcp.15644

APA

Rasmussen, L. D., Lebech, A. M., Øvrehus, A., Poulsen, B. K., Christensen, H. R., Nielsen, H., Johansen, I. S., Omland, L. H., Wiese, L., Helleberg, M., Storgaard, M., Dalager-Pedersen, M., Rasmussen, T. A., Benfield, T., Petersen, T. S., Andersen, Å. B., Gram, M. A., Stegger, M., Edslev, S. M., & Obel, N. (2023). Experience with sotrovimab treatment of SARS-CoV-2-infected patients in Denmark. British Journal of Clinical Pharmacology, 89(6), 1820-1833. https://doi.org/10.1111/bcp.15644

Vancouver

Rasmussen LD, Lebech AM, Øvrehus A, Poulsen BK, Christensen HR, Nielsen H et al. Experience with sotrovimab treatment of SARS-CoV-2-infected patients in Denmark. British Journal of Clinical Pharmacology. 2023;89(6):1820-1833. https://doi.org/10.1111/bcp.15644

Author

Rasmussen, Line Dahlerup ; Lebech, Anne Mette ; Øvrehus, Anne ; Poulsen, Birgitte Klindt ; Christensen, Hanne Rolighed ; Nielsen, Henrik ; Johansen, Isik Somuncu ; Omland, Lars Haukali ; Wiese, Lothar ; Helleberg, Marie ; Storgaard, Merete ; Dalager-Pedersen, Michael ; Rasmussen, Thomas A. ; Benfield, Thomas ; Petersen, Tonny Studsgaard ; Andersen, Åse Bengård ; Gram, Mie Agermose ; Stegger, Marc ; Edslev, Sofie Marie ; Obel, Niels. / Experience with sotrovimab treatment of SARS-CoV-2-infected patients in Denmark. In: British Journal of Clinical Pharmacology. 2023 ; Vol. 89, No. 6. pp. 1820-1833.

Bibtex

@article{b0907cfd852e4d84b998f8ff70eff45b,
title = "Experience with sotrovimab treatment of SARS-CoV-2-infected patients in Denmark",
abstract = "Aims: To evaluate the experience with use of sotrovimab following severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection in high-risk groups. Methods: In a nationwide, population-based cohort study, we identified all individuals treated with sotrovimab (N = 2933) and stratified them by 4 high-risk groups: (A) malignant haematological disease, (B) solid organ transplantation, (C) anti-CD20 therapy ≤1 year and (D) other risks. Cox regression analysis was used to calculate hazard ratios for hospitalization, death and associated prognostic factors. Results: Of 2933 sotrovimab-treated individuals, 83% belonged to high-risk groups (37.6% haematological malignancy, 27.4% solid organ transplantation and 17.5% treatment with anti-CD20 ≤1 year). Only 17.8% had other risks (11.8% were pregnant, 10.7% primary immunodeficiency, 21.2% other malignancy, 4.3% received anti-CD20 >1 year and 52.0% other/unknown causes). Within 90 days of infusion, 30.2% were hospitalized and 5.3% died. The main prognostic factors were the predefined high-risk groups, mainly malignant haematological disease and age ≥65 years. Number of COVID-19 vaccines (≥3) was associated with a decreased risk of hospitalization. The Delta but not the Omicron BA.2 variant was associated with a higher risk of death compared to the BA.1 variant. Conclusion: More than 90% of the patients treated with sotrovimab belonged to the very high-risk groups as described in the Danish guidelines. Sotrovimab-treated individuals remained at a high risk of hospitalization and death which was strongly associated with the underlying immunocompromised state and age. Having received >3 COVID-19 vaccines was association with decreased risk of death and hospitalization.",
keywords = "COVID-19, mAB, SARS-CoV-2, SARS-CoV-2 vaccines, sotrovimab",
author = "Rasmussen, {Line Dahlerup} and Lebech, {Anne Mette} and Anne {\O}vrehus and Poulsen, {Birgitte Klindt} and Christensen, {Hanne Rolighed} and Henrik Nielsen and Johansen, {Isik Somuncu} and Omland, {Lars Haukali} and Lothar Wiese and Marie Helleberg and Merete Storgaard and Michael Dalager-Pedersen and Rasmussen, {Thomas A.} and Thomas Benfield and Petersen, {Tonny Studsgaard} and Andersen, {{\AA}se Beng{\aa}rd} and Gram, {Mie Agermose} and Marc Stegger and Edslev, {Sofie Marie} and Niels Obel",
note = "Publisher Copyright: {\textcopyright} 2022 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.",
year = "2023",
doi = "10.1111/bcp.15644",
language = "English",
volume = "89",
pages = "1820--1833",
journal = "British Journal of Clinical Pharmacology, Supplement",
issn = "0264-3774",
publisher = "Wiley-Blackwell",
number = "6",

}

RIS

TY - JOUR

T1 - Experience with sotrovimab treatment of SARS-CoV-2-infected patients in Denmark

AU - Rasmussen, Line Dahlerup

AU - Lebech, Anne Mette

AU - Øvrehus, Anne

AU - Poulsen, Birgitte Klindt

AU - Christensen, Hanne Rolighed

AU - Nielsen, Henrik

AU - Johansen, Isik Somuncu

AU - Omland, Lars Haukali

AU - Wiese, Lothar

AU - Helleberg, Marie

AU - Storgaard, Merete

AU - Dalager-Pedersen, Michael

AU - Rasmussen, Thomas A.

AU - Benfield, Thomas

AU - Petersen, Tonny Studsgaard

AU - Andersen, Åse Bengård

AU - Gram, Mie Agermose

AU - Stegger, Marc

AU - Edslev, Sofie Marie

AU - Obel, Niels

N1 - Publisher Copyright: © 2022 The Authors. British Journal of Clinical Pharmacology published by John Wiley & Sons Ltd on behalf of British Pharmacological Society.

PY - 2023

Y1 - 2023

N2 - Aims: To evaluate the experience with use of sotrovimab following severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection in high-risk groups. Methods: In a nationwide, population-based cohort study, we identified all individuals treated with sotrovimab (N = 2933) and stratified them by 4 high-risk groups: (A) malignant haematological disease, (B) solid organ transplantation, (C) anti-CD20 therapy ≤1 year and (D) other risks. Cox regression analysis was used to calculate hazard ratios for hospitalization, death and associated prognostic factors. Results: Of 2933 sotrovimab-treated individuals, 83% belonged to high-risk groups (37.6% haematological malignancy, 27.4% solid organ transplantation and 17.5% treatment with anti-CD20 ≤1 year). Only 17.8% had other risks (11.8% were pregnant, 10.7% primary immunodeficiency, 21.2% other malignancy, 4.3% received anti-CD20 >1 year and 52.0% other/unknown causes). Within 90 days of infusion, 30.2% were hospitalized and 5.3% died. The main prognostic factors were the predefined high-risk groups, mainly malignant haematological disease and age ≥65 years. Number of COVID-19 vaccines (≥3) was associated with a decreased risk of hospitalization. The Delta but not the Omicron BA.2 variant was associated with a higher risk of death compared to the BA.1 variant. Conclusion: More than 90% of the patients treated with sotrovimab belonged to the very high-risk groups as described in the Danish guidelines. Sotrovimab-treated individuals remained at a high risk of hospitalization and death which was strongly associated with the underlying immunocompromised state and age. Having received >3 COVID-19 vaccines was association with decreased risk of death and hospitalization.

AB - Aims: To evaluate the experience with use of sotrovimab following severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) infection in high-risk groups. Methods: In a nationwide, population-based cohort study, we identified all individuals treated with sotrovimab (N = 2933) and stratified them by 4 high-risk groups: (A) malignant haematological disease, (B) solid organ transplantation, (C) anti-CD20 therapy ≤1 year and (D) other risks. Cox regression analysis was used to calculate hazard ratios for hospitalization, death and associated prognostic factors. Results: Of 2933 sotrovimab-treated individuals, 83% belonged to high-risk groups (37.6% haematological malignancy, 27.4% solid organ transplantation and 17.5% treatment with anti-CD20 ≤1 year). Only 17.8% had other risks (11.8% were pregnant, 10.7% primary immunodeficiency, 21.2% other malignancy, 4.3% received anti-CD20 >1 year and 52.0% other/unknown causes). Within 90 days of infusion, 30.2% were hospitalized and 5.3% died. The main prognostic factors were the predefined high-risk groups, mainly malignant haematological disease and age ≥65 years. Number of COVID-19 vaccines (≥3) was associated with a decreased risk of hospitalization. The Delta but not the Omicron BA.2 variant was associated with a higher risk of death compared to the BA.1 variant. Conclusion: More than 90% of the patients treated with sotrovimab belonged to the very high-risk groups as described in the Danish guidelines. Sotrovimab-treated individuals remained at a high risk of hospitalization and death which was strongly associated with the underlying immunocompromised state and age. Having received >3 COVID-19 vaccines was association with decreased risk of death and hospitalization.

KW - COVID-19

KW - mAB

KW - SARS-CoV-2

KW - SARS-CoV-2 vaccines

KW - sotrovimab

U2 - 10.1111/bcp.15644

DO - 10.1111/bcp.15644

M3 - Journal article

C2 - 36519217

AN - SCOPUS:85146334563

VL - 89

SP - 1820

EP - 1833

JO - British Journal of Clinical Pharmacology, Supplement

JF - British Journal of Clinical Pharmacology, Supplement

SN - 0264-3774

IS - 6

ER -

ID: 341060524