Please use this identifier to cite or link to this item: https://hdl.handle.net/10216/154867
Author(s): Pagano, L
Salmanton-García, J
Marchesi, F
Busca, A
Corradini, P
Hoenigl, M
Klimko, N
Koehler, P
Pagliuca, A
Passamonti, F
Verga, L
Víšek, B
Ilhan, O
Nadali, G
Weinbergerová, B
Córdoba-Mascuñano, R
Marchetti, M
Collins, GP
Farina, F
Cattaneo, C
Cabirta, A
Gomes-Silva, M
Itri, F
van Doesum, J
Ledoux, MP
Cernan, M
Jakšic, O
Duarte, RF
Magliano, G
Omrani, AS
Fracchiolla, NS
Kulasekararaj, A
Valkovic, T
Poulsen, CB
Machado, M
Glenthøj, A
Stoma, I
Rácil, Z
Piukovics, K
Navrátil, M
Emarah, Z
Sili, U
Maertens, J
Blennow, O
Bergantim, R
García-Vidal, C
Prezioso, L
Guidetti, A
del Principe, MI
Popova, M
de Jonge, N
Ormazabal-Vélez, I
Fernández, N
Falces-Romero, I
Cuccaro, A
Meers, S
Buquicchio, C
Antic, D
Al-Khabori, M
García-Sanz, R
Biernat, MM
Tisi, MC
Sal, E
Rahimli, L
Colovic, N
Schönlein, M
Calbacho, M
Tascini, C
Miranda-Castillo, C
Khanna, N
Méndez, GA
Petzer, V
Novák, J
Besson, C
Duléry, R
Lamure, S
Nucci, M
Zambrotta, G
Žák, P
Seval, GC
Bonuomo, V
Mayer, J
López-García, A
Sacchi, MV
Booth, S
Ciceri, F
Oberti, M
Salvini, M
Izuzquiza, M
Nunes-Rodrigues, R
Ammatuna, E
Obr, A
Herbrecht, R
Núñez-Martín-Buitrago, L
Mancini, V
Shwaylia, H
Sciumè, M
Essame, J
Nygaard, M
Batinic, J
Gonzaga, Y
Regalado-Artamendi, I
Karlsson, LK
Shapetska, M
Hanakova, M
El-Ashwah, S
Borbényi, Z
Çolak, GM
Nordlander, A
Dragonetti, G
Maraglino, AME
Rinaldi, A
De Ramón-Sánchez, C
Cornely, OA
Finizio, O
Fazzi, R
Sapienza, G
Chauchet, A
Van Praet, J
Prattes, J
Dargenio, M
Rossi, C
Shirinova, A
Malak, S
Tafuri, A
Ommen, HB
Bologna, S
Khedr, RA
Choquet, S
Joly, B
Ceesay, MM
Philippe, L
Kho, CS
Desole, M
Tsirigotis, P
Otaševic, V
Borducchi, DMM
Antoniadou, A
Gaziev, J
Almaslamani, MA
García-Poutón, N
Paterno, G
Torres-López, A
Tarantini, G
Mellinghoff, S
Gräfe, S
Börschel, N
Passweg, J
Merelli, M
Barac, A
Wolf, D
Shaikh, MU
Thiéblemont, C
Bernard, S
Funke, VAM
Daguindau, E
Khostelidi, S
Nucci, FM
Martín-González, JA
Landau, M
Soussain, C
Laureana, C
Lacombe, K
Kohn, M
Aliyeva, G
Piedimonte, M
Fouquet, G
Rêgo, M
Hoell-Neugebauer, B
Cartron, G
Pinto, F
Alburquerque, AM
Passos, J
Yilmaz, AF
Redondo-Izal, AM
Altuntas, F
Heath, C
Kolditz, M
Schalk, E
Guolo, F
Karthaus, M
Della Pepa, R
Vinh, D
Noël, N
Deau Fischer, B
Drenou, B
Mitra, ME
Meletiadis, J
Bilgin, YM
Jindra, P
Espigado, I
Drgona, L
Serris, A
Di Blasi, R
Ali, N
Title: COVID-19 infection in adult patients with hematological malignancies: a European Hematology Association Survey (EPICOVIDEHA)
Publisher: BMC
Issue Date: 2021
Abstract: Background: Patients with hematological malignancies (HM) are at high risk of mortality from SARS-CoV-2 disease 2019 (COVID-19). A better understanding of risk factors for adverse outcomes may improve clinical management in these patients. We therefore studied baseline characteristics of HM patients developing COVID-19 and analyzed predictors of mortality. Methods: The survey was supported by the Scientific Working Group Infection in Hematology of the European Hematology Association (EHA). Eligible for the analysis were adult patients with HM and laboratory-confirmed COVID-19 observed between March and December 2020. Results: The study sample includes 3801 cases, represented by lymphoproliferative (mainly non-Hodgkin lymphoma n = 1084, myeloma n = 684 and chronic lymphoid leukemia n = 474) and myeloproliferative malignancies (mainly acute myeloid leukemia n = 497 and myelodysplastic syndromes n = 279). Severe/critical COVID-19 was observed in 63.8% of patients (n = 2425). Overall, 2778 (73.1%) of the patients were hospitalized, 689 (18.1%) of whom were admitted to intensive care units (ICUs). Overall, 1185 patients (31.2%) died. The primary cause of death was COVID-19 in 688 patients (58.1%), HM in 173 patients (14.6%), and a combination of both COVID-19 and progressing HM in 155 patients (13.1%). Highest mortality was observed in acute myeloid leukemia (199/497, 40%) and myelodysplastic syndromes (118/279, 42.3%). The mortality rate significantly decreased between the first COVID-19 wave (March–May 2020) and the second wave (October–December 2020) (581/1427, 40.7% vs. 439/1773, 24.8%, p value < 0.0001). In the multivariable analysis, age, active malignancy, chronic cardiac disease, liver disease, renal impairment, smoking history, and ICU stay correlated with mortality. Acute myeloid leukemia was a higher mortality risk than lymphoproliferative diseases. Conclusions: This survey confirms that COVID-19 patients with HM are at high risk of lethal complications. However, improved COVID-19 prevention has reduced mortality despite an increase in the number of reported cases.
Subject: COVID-19
EHA
Epidemiology
Hematological malignancies
Pandemic
DOI: 10.1186/s13045-021-01177-0
URI: https://hdl.handle.net/10216/154867
Source: Journal of Hematology and Oncology, vol.14(1):168
Document Type: Artigo em Revista Científica Internacional
Rights: openAccess
License: https://creativecommons.org/licenses/by/4.0/
Appears in Collections:I3S - Artigo em Revista Científica Internacional

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