4.6 Article

Remdesivir or Nirmatrelvir/Ritonavir Therapy for Omicron SARS-CoV-2 Infection in Hematological Patients and Cell Therapy Recipients

Journal

VIRUSES-BASEL
Volume 15, Issue 10, Pages -

Publisher

MDPI
DOI: 10.3390/v15102066

Keywords

remdesivir; nirmatrelvir/ritonavir; molnupiravir SARS-CoV-2 vaccines; Omicron; respiratory virus; hematological malignancies; allogeneic stem cell transplantation; autologous stem cell transplantation; COVID-19; mRNA vaccine; immunocompromised patients

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This study analyzed the outcomes of hematological patients with SARS-CoV-2 infection who received treatment with remdesivir or nirmatrelvir/ritonavir. The results showed that nirmatrelvir/ritonavir was safe and effective for treating mild cases, while remdesivir was preferred for moderate to severe cases with a higher mortality rate. Factors such as male gender, corticosteroid use, and co-infection were associated with worse outcomes in patients treated with remdesivir.
Background: Scarce data exist that analyze the outcomes of hematological patients with SARS-CoV-2 infection during the Omicron variant period who received treatment with remdesivir or nirmatrelvir/ritonavir. Methods: This study aims to address this issue by using a retrospective observational registry, created by the Spanish Hematopoietic Stem Cell Transplantation and Cell Therapy Group, spanning from 27 December 2021 to 30 April 2023. Results: This study included 466 patients, 243 (52%) who were treated with remdesivir and 223 (48%) with nirmatrelvir/ritonavir. Nirmatrelvir/ritonavir was primarily used for mild cases, resulting in a lower COVID-19-related mortality rate (1.3%), while remdesivir was preferred for moderate to severe cases (40%), exhibiting a higher mortality rate (9%). A multivariate analysis in the remdesivir cohort showed that male gender (odds ratio (OR) 0.35, p = 0.042) correlated with a lower mortality risk, while corticosteroid use (OR 9.4, p < 0.001) and co-infection (OR 2.8, p = 0.047) were linked to a higher mortality risk. Prolonged virus shedding was common, with 52% of patients shedding the virus for more than 25 days. In patients treated with remdesivir, factors associated with prolonged shedding included B-cell malignancy as well as underlying disease, severe disease, a later onset of and shorter duration of remdesivir treatment and a higher baseline viral load. Nirmatrelvir/ritonavir demonstrated a comparable safety profile to remdesivir, despite a higher risk of drug interactions. Conclusions: Nirmatrelvir/ritonavir proved to be a safe and effective option for treating mild cases in the outpatient setting, while remdesivir was preferred for severe cases, where corticosteroids and co-infection significantly predicted worse outcomes. Despite antiviral therapy, prolonged shedding remains a matter of concern.

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