Passive pre-exposure immunization by tixagevimab/cilgavimab in patients with hematological malignancy and COVID-19: matched-paired analysis in the EPICOVIDEHA registry

  • F. Marchesi
  • , J. Salmanton-Garcia*
  • , C. Buquicchio
  • , F. Itri
  • , C. Besson
  • , J. Davila-Valls
  • , S. Martin-Perez
  • , Luana Fianchi
  • , L. Rahimli
  • , G. Tarantini
  • , F. I. Grifoni
  • , M. Sciume
  • , J. Labrador
  • , R. Cordoba
  • , A. Lopez-Garcia
  • , N. S. Fracchiolla
  • , F. Farina
  • , E. Ammatuna
  • , Antonella Cingolani
  • , D. Garcia-Bordallo
  • S. K. Grafe, Y. M. Bilgin, M. Dargenio, T. J. Gonzalez-Lopez, A. Guidetti, T. Lahmer, E. Lavilla-Rubira, Mendez G. -A., L. Prezioso, M. Schonlein, Doesum J. Van, D. Wolf, D. S. Hersby, F. Magyari, Praet J. Van, V. Petzer, C. Tascini, I. Falces-Romero, A. Glenthoj, O. A. Cornely, Livio Pagano
*Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivistaArticolo

Abstract

Only few studies have analyzed the efficacy of tixagevimab/cilgavimab to prevent severe Coronavirus disease 2019 (COVID-19) and related complications in hematologic malignancies (HM) patients. Here, we report cases of breakthrough COVID-19 after prophylactic tixagevimab/cilgavimab from the EPICOVIDEHA registry). We identified 47 patients that had received prophylaxis with tixagevimab/cilgavimab in the EPICOVIDEHA registry. Lymphoproliferative disorders (44/47, 93.6%) were the main underlying HM. SARS-CoV-2 strains were genotyped in 7 (14.9%) cases only, and all belonged to the omicron variant. Forty (85.1%) patients had received vaccinations prior to tixagevimab/cilgavimab, the majority of them with at least two doses. Eleven (23.4%) patients had a mild SARS-CoV-2 infection, 21 (44.7%) a moderate infection, while 8 (17.0%) had severe infection and 2 (4.3%) critical. Thirty-six (76.6%) patients were treated, either with monoclonal antibodies, antivirals, corticosteroids, or with combination schemes. Overall, 10 (21.3%) were admitted to a hospital. Among these, two (4.3%) were transferred to intensive care unit and one (2.1%) of them died. Our data seem to show that the use of tixagevimab/cilgavimab may lead to a COVID-19 severity reduction in HM patients; however, further studies should incorporate further HM patients to confirm the best drug administration strategies in immunocompromised patients.
Lingua originaleInglese
pagine (da-a)32-37
Numero di pagine6
RivistaJournal of Hematology and Oncology
Volume16
Numero di pubblicazione1
DOI
Stato di pubblicazionePubblicato - 2023

All Science Journal Classification (ASJC) codes

  • Ematologia
  • Biologia Molecolare
  • Oncologia
  • Ricerca sul Cancro

Keywords

  • COVID-19
  • Hematologic malignancies
  • Passive immunization
  • Tixagevimab/cilgavimab

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