TY - JOUR
T1 - Improved outcome of COVID-19 over time in patients treated with CAR T-cell therapy
T2 - Update of the European COVID-19 multicenter study on behalf of the European Society for Blood and Marrow Transplantation (EBMT) Infectious Diseases Working Party (IDWP) and the European Hematology Association (EHA) Lymphoma Group
AU - Spanjaart, Anne Mea
AU - Ljungman, Per
AU - Tridello, Gloria
AU - Schwartz, Juana
AU - Martinez-Cibrián, Nuria
AU - Barba, Pere
AU - Kwon, Mi
AU - Lopez-Corral, Lucia
AU - Martinez-Lopez, Joaquin
AU - Ferra, Christelle
AU - Di Blasi, Roberta
AU - Ghesquieres, Hervé
AU - Mutsaers, Pim
AU - Calkoen, Friso
AU - Jak, Margot
AU - van Doesum, Jaap
AU - Vermaat, Joost S.P.
AU - van der Poel, Marjolein
AU - Maertens, Johan
AU - Gambella, Massimiliano
AU - Metafuni, Elisabetta
AU - Ciceri, Fabio
AU - Saccardi, Riccardo
AU - Nicholson, Emma
AU - Tholouli, Eleni
AU - Matthew, Collin
AU - Potter, Victoria
AU - Bloor, Adrian
AU - Besley, Caroline
AU - Roddie, Claire
AU - Wilson, Keith
AU - Nagler, Arnon
AU - Campos, Antonio
AU - Petersen, Soeren Lykke
AU - Folber, Frantisek
AU - Bader, Peter
AU - Finke, Jurgen
AU - Kroger, Nicolaus
AU - Knelange, Nina
AU - de La Camara, Rafael
AU - Kersten, Marie José
AU - Mielke, Stephan
N1 - Publisher Copyright:
© The Author(s) 2024.
PY - 2024
Y1 - 2024
N2 - COVID-19 has been associated with high mortality in patients treated with Chimeric Antigen Receptor (CAR) T-cell therapy for hematologic malignancies. Here, we investigated whether the outcome has improved over time with the primary objective of assessing COVID-19-attributable mortality in the Omicron period of 2022 compared to previous years. Data for this multicenter study were collected using the MED-A and COVID-19 report forms developed by the EBMT. One-hundred-eighty patients were included in the analysis, 39 diagnosed in 2020, 35 in 2021 and 106 in 2022. The median age was 58.9 years (min-max: 5.2–78.4). There was a successive decrease in COVID-19-related mortality over time (2020: 43.6%, 2021: 22.9%, 2022: 7.5%) and in multivariate analysis year of infection was the strongest predictor of survival (p = 0.0001). Comparing 2022 with 2020–2021, significantly fewer patients had lower respiratory symptoms (21.7% vs 37.8%, p = 0.01), needed oxygen support (25.5% vs 43.2%, p = 0.01), or were admitted to ICU (5.7% vs 33.8%, p = 0.0001). Although COVID-19-related mortality has decreased over time, CAR T-cell recipients remain at higher risk for complications than the general population. Consequently, vigilant monitoring for COVID-19 in patients undergoing B-cell-targeting CAR T-cell treatment is continuously recommended ensuring optimal prevention of infection and advanced state-of-the art treatment when needed.
AB - COVID-19 has been associated with high mortality in patients treated with Chimeric Antigen Receptor (CAR) T-cell therapy for hematologic malignancies. Here, we investigated whether the outcome has improved over time with the primary objective of assessing COVID-19-attributable mortality in the Omicron period of 2022 compared to previous years. Data for this multicenter study were collected using the MED-A and COVID-19 report forms developed by the EBMT. One-hundred-eighty patients were included in the analysis, 39 diagnosed in 2020, 35 in 2021 and 106 in 2022. The median age was 58.9 years (min-max: 5.2–78.4). There was a successive decrease in COVID-19-related mortality over time (2020: 43.6%, 2021: 22.9%, 2022: 7.5%) and in multivariate analysis year of infection was the strongest predictor of survival (p = 0.0001). Comparing 2022 with 2020–2021, significantly fewer patients had lower respiratory symptoms (21.7% vs 37.8%, p = 0.01), needed oxygen support (25.5% vs 43.2%, p = 0.01), or were admitted to ICU (5.7% vs 33.8%, p = 0.0001). Although COVID-19-related mortality has decreased over time, CAR T-cell recipients remain at higher risk for complications than the general population. Consequently, vigilant monitoring for COVID-19 in patients undergoing B-cell-targeting CAR T-cell treatment is continuously recommended ensuring optimal prevention of infection and advanced state-of-the art treatment when needed.
UR - http://www.scopus.com/inward/record.url?scp=85199401551&partnerID=8YFLogxK
U2 - 10.1038/s41375-024-02336-1
DO - 10.1038/s41375-024-02336-1
M3 - Article
C2 - 39043963
AN - SCOPUS:85199401551
SN - 0887-6924
VL - 38
SP - 1985
EP - 1991
JO - Leukemia
JF - Leukemia
IS - 9
ER -