Real-Life Comparison of Antivirals for SARS-CoV-2 Omicron Infection in Patients With Hematologic Malignancies.

COVID-19 Omicron nirmatrelvir/ritonavir outcome phenotypes

Journal

Influenza and other respiratory viruses
ISSN: 1750-2659
Titre abrégé: Influenza Other Respir Viruses
Pays: England
ID NLM: 101304007

Informations de publication

Date de publication:
2024
Historique:
revised: 17 01 2024
received: 04 08 2023
accepted: 27 01 2024
medline: 12 3 2024
pubmed: 12 3 2024
entrez: 12 3 2024
Statut: ppublish

Résumé

We aimed to describe a cohort of hematologic patients with COVID-19 treated with antivirals early. Non-interventional chart review study. Comparison of baseline characteristics and outcomes in high-risk hematologic patients treated with remdesivir between December 2021 and April 2022 versus those treated with nirmatrelvir/ritonavir between May and August 2022. Eighty-three patients were analyzed. Forty-two received remdesivir, and 41 nirmatrelvir/ritonavir. Patients with remdesivir were younger, vaccinated with lower number of doses, and received prior corticosteroids less frequently and sotrovimab, hyperimmune plasma and corticosteroids more often. Viral shedding median (IQR) duration was 18 (13-23) and 11 (8-21) days in the remdesivir and nirmatrelvir/ritonavir groups, respectively (p = 0.004). Median (IQR) Ct values before treatment were similar in both groups. Within 5 days of treatment, median (IQR) Ct values were 26 (23-29) and 33 (30-37) in the remdesivir and nirmatrelvir/ritonavir groups, respectively (p < 0.0001). All patients were hospitalized for remdesivir administration and only four (9.8%) in the nirmatrelvir/ritonavir group. The overall outcomes in this cohort of COVID-19 patients with Omicron variant was good, as no patient needed oxygen or ICU admission. One patient in remdesivir group died from septic shock. No severe adverse event was recorded in both treatment groups. Patients with hematologic malignancies and non-severe COVID-19 who received nirmatrelvir/ritonavir experienced faster decrease in viral load and shorter viral shedding. Furthermore, besides the advantage of oral administration, nirmatrelvir/ritonavir administration reduced the need of hospital admission.

Sections du résumé

BACKGROUND BACKGROUND
We aimed to describe a cohort of hematologic patients with COVID-19 treated with antivirals early.
METHODS METHODS
Non-interventional chart review study. Comparison of baseline characteristics and outcomes in high-risk hematologic patients treated with remdesivir between December 2021 and April 2022 versus those treated with nirmatrelvir/ritonavir between May and August 2022.
RESULTS RESULTS
Eighty-three patients were analyzed. Forty-two received remdesivir, and 41 nirmatrelvir/ritonavir. Patients with remdesivir were younger, vaccinated with lower number of doses, and received prior corticosteroids less frequently and sotrovimab, hyperimmune plasma and corticosteroids more often. Viral shedding median (IQR) duration was 18 (13-23) and 11 (8-21) days in the remdesivir and nirmatrelvir/ritonavir groups, respectively (p = 0.004). Median (IQR) Ct values before treatment were similar in both groups. Within 5 days of treatment, median (IQR) Ct values were 26 (23-29) and 33 (30-37) in the remdesivir and nirmatrelvir/ritonavir groups, respectively (p < 0.0001). All patients were hospitalized for remdesivir administration and only four (9.8%) in the nirmatrelvir/ritonavir group. The overall outcomes in this cohort of COVID-19 patients with Omicron variant was good, as no patient needed oxygen or ICU admission. One patient in remdesivir group died from septic shock. No severe adverse event was recorded in both treatment groups.
CONCLUSIONS CONCLUSIONS
Patients with hematologic malignancies and non-severe COVID-19 who received nirmatrelvir/ritonavir experienced faster decrease in viral load and shorter viral shedding. Furthermore, besides the advantage of oral administration, nirmatrelvir/ritonavir administration reduced the need of hospital admission.

Identifiants

pubmed: 38468434
doi: 10.1111/irv.13264
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e13264

Subventions

Organisme : Instituto de Salud Carlos III
ID : JR20/00012
Organisme : Instituto de Salud Carlos III
ID : PI21/00498
Organisme : Instituto de Salud Carlos III
ID : PI21/01640
Organisme : Instituto de Salud Carlos III
ID : RH RH042953
Organisme : FEDER
Organisme : Agència de Gestión de Ayudas Universitarias y de Investigación
ID : SGR 01324 Q5856414G
Organisme : La Ligue Nationale contre le Cancer
ID : AAPMRC 2022/OP
Organisme : La Direction de l'Assistance Publique - Hôpitaux de Paris

Informations de copyright

© 2024 The Authors. Influenza and Other Respiratory Viruses published by John Wiley & Sons Ltd.

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Auteurs

Tommaso Francesco Aiello (TF)

Infectious Diseases Department, Hospital Clinic of Barcelona-IDIBAPS, Universitat de Barcelona, Barcelona, Spain.

Olivier Peyrony (O)

Emergency Department, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Paris, France.

Mariana Chumbita (M)

Infectious Diseases Department, Hospital Clinic of Barcelona-IDIBAPS, Universitat de Barcelona, Barcelona, Spain.

Patricia Monzó (P)

Infectious Diseases Department, Hospital Clinic of Barcelona-IDIBAPS, Universitat de Barcelona, Barcelona, Spain.

Carlos Lopera (C)

Infectious Diseases Department, Hospital Clinic of Barcelona-IDIBAPS, Universitat de Barcelona, Barcelona, Spain.

Pedro Puerta-Alcalde (P)

Infectious Diseases Department, Hospital Clinic of Barcelona-IDIBAPS, Universitat de Barcelona, Barcelona, Spain.

Laura Magnano (L)

Department of Haematology, Hospital Clinic of Barcelona-IDIBAPS, University of Barcelona, Barcelona, Spain.

Francesc Fernández-Avilés (F)

Department of Haematology, Hospital Clinic of Barcelona-IDIBAPS, University of Barcelona, Barcelona, Spain.

Genoveva Cuesta (G)

Microbiology Department, Hospital Clinic, University of Barcelona, ISGLOBAL, Barcelona, Spain.

Montse Tuset (M)

Department of Pharmacy, Hospital Clinic of Barcelona-IDIBAPS, University of Barcelona, Barcelona, Spain.

Josep Mensa (J)

Infectious Diseases Department, Hospital Clinic of Barcelona-IDIBAPS, Universitat de Barcelona, Barcelona, Spain.

Jordi Esteve (J)

Department of Haematology, Hospital Clinic of Barcelona-IDIBAPS, University of Barcelona, Barcelona, Spain.

Maria Angeles Marcos (MA)

Department of Haematology, Hospital Clinic of Barcelona-IDIBAPS, University of Barcelona, Barcelona, Spain.

Alex Soriano (A)

Infectious Diseases Department, Hospital Clinic of Barcelona-IDIBAPS, Universitat de Barcelona, Barcelona, Spain.
Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Barcelona, Spain.

Carolina Garcia-Vidal (C)

Infectious Diseases Department, Hospital Clinic of Barcelona-IDIBAPS, Universitat de Barcelona, Barcelona, Spain.
Facultat de Medicina i Ciències de la Salut, Universitat de Barcelona, Barcelona, Spain.

Classifications MeSH