TY - JOUR
T1 - Passive pre-exposure immunization by tixagevimab/cilgavimab in patients with hematological malignancy and COVID-19: matched-paired analysis in the EPICOVIDEHA registry
AU - Marchesi, F.
AU - Salmanton-Garcia, J.
AU - Buquicchio, C.
AU - Itri, F.
AU - Besson, C.
AU - Davila-Valls, J.
AU - Martin-Perez, S.
AU - Fianchi, Luana
AU - Rahimli, L.
AU - Tarantini, G.
AU - Grifoni, F. I.
AU - Sciume, M.
AU - Labrador, J.
AU - Cordoba, R.
AU - Lopez-Garcia, A.
AU - Fracchiolla, N. S.
AU - Farina, F.
AU - Ammatuna, E.
AU - Cingolani, Antonella
AU - Garcia-Bordallo, D.
AU - Grafe, S. K.
AU - Bilgin, Y. M.
AU - Dargenio, M.
AU - Gonzalez-Lopez, T. J.
AU - Guidetti, A.
AU - Lahmer, T.
AU - Lavilla-Rubira, E.
AU - -A., Mendez G.
AU - Prezioso, L.
AU - Schonlein, M.
AU - Van, Doesum J.
AU - Wolf, D.
AU - Hersby, D. S.
AU - Magyari, F.
AU - Van, Praet J.
AU - Petzer, V.
AU - Tascini, C.
AU - Falces-Romero, I.
AU - Glenthoj, A.
AU - Cornely, O. A.
AU - Pagano, Livio
PY - 2023
Y1 - 2023
N2 - 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.
AB - 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.
KW - COVID-19
KW - Hematologic malignancies
KW - Passive immunization
KW - Tixagevimab/cilgavimab
KW - COVID-19
KW - Hematologic malignancies
KW - Passive immunization
KW - Tixagevimab/cilgavimab
UR - https://publicatt.unicatt.it/handle/10807/235312
UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=85151381738&origin=inward
UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85151381738&origin=inward
U2 - 10.1186/s13045-023-01423-7
DO - 10.1186/s13045-023-01423-7
M3 - Article
SN - 1756-8722
VL - 16
SP - 32
EP - 37
JO - Journal of Hematology and Oncology
JF - Journal of Hematology and Oncology
IS - 1
ER -