Outcome of early treatment of SARS‐CoV‐2 infection in patients with haematological disorders

Author:

Mikulska Malgorzata12ORCID,Testi Diletta34,Russo Chiara12,Balletto Elisa12,Sepulcri Chiara12,Bussini Linda34,Dentone Chiara2,Magne Federica2,Policarpo Sílvia5,Campoli Caterina3,Miselli Filippo34,Cilli Alessandro34,Ghiggi Chiara6,Aquino Sara6,Di Grazia Carmen6,Giannella Maddalena34,Giacobbe Daniele Roberto12,Vena Antonio12,Raiola Anna Maria6,Bonifazi Francesca78,Zinzani Pierluigi78ORCID,Cavo Michele78,Lemoli Roberto29ORCID,Angelucci Emanuele6ORCID,Viale Pierluigi34,Bassetti Matteo12,Bartoletti Michele1011

Affiliation:

1. Division of Infectious Diseases, Department of Health Sciences (DISSAL) University of Genova Genoa Italy

2. IRCCS Ospedale Policlinico San Martino Genoa Italy

3. Infectious Diseases Unit IRCCS Azienda Ospedaliero‐Universitaria di Bologna, Policlinico di Sant'Orsola Bologna Italy

4. Department of Medical and Surgical Sciences Alma Mater Studiorum University of Bologna Bologna Italy

5. Infectious Diseases Department Centro Hospitalar Universitário São João Porto Portugal

6. Ematologia e Terapie Cellulari, IRCCS Ospedale Policlinico San Martino Genoa Italy

7. IRCCS—Azienda Ospedaliero‐Universitaria di Bologna Bologna Italy

8. Institute of Hematology ‘L. e A. Seràgnoli’ University of Bologna Bologna Italy

9. Department of Internal Medicine (DiMI) Clinic of Hematology, University of Genoa Genoa Italy

10. IRCCS Humanitas Research Hospital Milan Italy

11. Department of Biomedical Sciences Humanitas University Milan Italy

Abstract

SummaryOutcome of early treatment of COVID‐19 with antivirals or anti‐spike monoclonal antibodies (MABs) in patients with haematological malignancies (HM) is unknown. A retrospective study of HM patients treated for mild/moderate COVID‐19 between March 2021 and July 2022 was performed. The main composite end‐point was treatment failure (severe COVID‐19 or COVID‐19‐related death). We included 328 consecutive patients who received MABs (n = 120, 37%; sotrovimab, n = 73) or antivirals (n = 208, 63%; nirmatrelvir/ritonavir, n = 116) over a median of two days after symptoms started; 111 (33.8%) had non‐Hodgkin lymphoma (NHL); 89 (27%) were transplant/CAR‐T (chimaeric antigen receptor T‐cell therapy) recipients. Most infections (n = 309, 94%) occurred during the Omicron period. Failure developed in 31 patients (9.5%). Its independent predictors were older age, fewer vaccine doses, and treatment with MABs. Rate of failure was lower in the Omicron versus the pre‐Omicron period (7.8% versus 36.8%, p < 0.001). During the Omicron period, predictors of failure were age, fewer vaccine doses and diagnosis of acute myeloid leukaemia/myelodysplastic syndrome (AML/MDS). Independent predictors of longer viral shedding were age, comorbidities, hospital admission at diagnosis, NHL/CLL, treatment with MABs. COVID‐19‐associated mortality was 3.4% (n = 11). The mortality in those who developed severe COVID‐19 after early treatment was 26% in the Omicron period. Patients with HM had a significant risk of failure of early treatment, even during the Omicron period, with high mortality rate.

Publisher

Wiley

Subject

Hematology

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