LIVIVO - The Search Portal for Life Sciences

zur deutschen Oberfläche wechseln
Advanced search

Search results

Result 1 - 4 of total 4

Search options

  1. Article ; Online: Impact of SARS-CoV-2 vaccination and monoclonal antibodies on outcome post-CD19-directed CAR T-cell therapy: an EPICOVIDEHA survey.

    van Doesum, Jaap A / Salmanton-García, Jon / Marchesi, Francesco / Di Blasi, Roberta / Falces-Romero, Iker / Cabirta, Alba / Farina, Francesca / Besson, Caroline / Weinbergerová, Barbora / Van Praet, Jens / Schönlein, Martin / López-García, Alberto / Lamure, Sylvain / Guidetti, Anna / De Ramón-Sánchez, Cristina / Batinić, Josip / Gavriilaki, Eleni / Tragiannidis, Athanasios / Tisi, Maria Chiara /
    Plantefeve, Gaëtan / Petzer, Verena / Ormazabal-Vélez, Irati / Marques de Almeida, Joyce / Marchetti, Monia / Maertens, Johan / Machado, Marina / Kulasekararaj, Austin / Hernández-Rivas, José-Ángel / Gomes da Silva, Maria / Fernández, Noemí / Espigado, Ildefonso / Drgoňa, Ľuboš / Dragonetti, Giulia / Metafuni, Elisabetta / Calbacho, Maria / Blennow, Ola / Wolf, Dominik / van Anrooij, Bjorn / Nunes Rodrigues, Raquel / Nordlander, Anna / Martín-González, Juan-Alberto / Liévin, Raphaël / Jiménez, Moraima / Gräfe, Stefanie K / García-Sanz, Ramón / Córdoba, Raúl / Rahimli, Laman / van Meerten, Tom / Cornely, Oliver A / Pagano, Livio

    Blood advances

    2023  Volume 7, Issue 11, Page(s) 2645–2655

    Abstract: Patients with previous CD19-directed chimeric antigen receptor (CAR) T-cell therapy have a prolonged vulnerability to viral infections. Coronavirus disease 2019 (COVID-19) has a great impact and has previously been shown to cause high mortality in this ... ...

    Abstract Patients with previous CD19-directed chimeric antigen receptor (CAR) T-cell therapy have a prolonged vulnerability to viral infections. Coronavirus disease 2019 (COVID-19) has a great impact and has previously been shown to cause high mortality in this population. Until now, real-world data on the impact of vaccination and treatment on patients with COVID-19 after CD19-directed CAR T-cell therapy are lacking. Therefore, this multicenter, retrospective study was conducted with data from the EPICOVIDEHA survey. Sixty-four patients were identified. The overall mortality caused by COVID-19 was 31%. Patients infected with the Omicron variant had a significantly lower risk of death due to COVID-19 compared with patients infected with previous variants (7% vs 58% [P = .012]). Twenty-six patients were vaccinated at the time of the COVID-19 diagnosis. Two vaccinations showed a marked but unsignificant reduction in the risk of COVID-19-caused mortality (33.3% vs 14.2% [P = .379]). In addition, the course of the disease appears milder with less frequent intensive care unit admissions (39% vs 14% [P = .054]) and a shorter duration of hospitalization (7 vs 27.5 days [P = .022]). Of the available treatment options, only monoclonal antibodies seemed to be effective at reducing mortality from 32% to 0% (P = .036). We conclude that survival rates of CAR T-cell recipients with COVID-19 improved over time and that the combination of prior vaccination and monoclonal antibody treatment significantly reduces their risk of death. This trial was registered at www.clinicaltrials.gov as #NCT04733729.
    MeSH term(s) Humans ; COVID-19/therapy ; COVID-19 Testing ; COVID-19 Vaccines ; Immunotherapy, Adoptive ; Retrospective Studies ; SARS-CoV-2 ; Vaccination ; Adaptor Proteins, Signal Transducing ; Antibodies, Monoclonal ; Antigens, CD19
    Chemical Substances COVID-19 Vaccines ; Adaptor Proteins, Signal Transducing ; Antibodies, Monoclonal ; Antigens, CD19
    Language English
    Publishing date 2023-04-14
    Publishing country United States
    Document type Multicenter Study ; Journal Article
    ZDB-ID 2915908-8
    ISSN 2473-9537 ; 2473-9529
    ISSN (online) 2473-9537
    ISSN 2473-9529
    DOI 10.1182/bloodadvances.2022009578
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  2. Article ; Online: COVID-19 in adult acute myeloid leukemia patients: a long-term follow-up study from the European Hematology Association survey (EPICOVIDEHA).

    Marchesi, Francesco / Salmanton-García, Jon / Emarah, Ziad / Piukovics, Klára / Nucci, Marcio / López-García, Alberto / Ráčil, Zdeněk / Farina, Francesca / Popova, Marina / Zompi, Sofia / Audisio, Ernesta / Ledoux, Marie-Pierre / Verga, Luisa / Weinbergerová, Barbora / Szotkovski, Tomas / Da Silva, Maria Gomes / Fracchiolla, Nicola / De Jonge, Nick / Collins, Graham /
    Marchetti, Monia / Magliano, Gabriele / García-Vidal, Carolina / Biernat, Monika M / Van Doesum, Jaap / Machado, Marina / Demirkan, Fatih / Al-Khabori, Murtadha / Žák, Pavel / Víšek, Benjamín / Stoma, Igor / Méndez, Gustavo-Adolfo / Maertens, Johan / Khanna, Nina / Espigado, Ildefonso / Dragonetti, Giulia / Fianchi, Luana / Del Principe, Maria Ilaria / Cabirta, Alba / Ormazabal-Vélez, Irati / Jaksic, Ozren / Buquicchio, Caterina / Bonuomo, Valentina / Batinić, Josip / Omrani, Ali S / Lamure, Sylvain / Finizio, Olimpia / Fernández, Noemí / Falces-Romero, Iker / Blennow, Ola / Bergantim, Rui / Ali, Natasha / Win, Sein / Van Praet, Jens / Tisi, Maria Chiara / Shirinova, Ayten / Schönlein, Martin / Prattes, Juergen / Piedimonte, Monica / Petzer, Verena / Navrátil, Milan / Kulasekararaj, Austin / Jindra, Pavel / Sramek, Jiří / Glenthøj, Andreas / Fazzi, Rita / De Ramón-Sánchez, Cristina / Cattaneo, Chiara / Calbacho, Maria / Bahr, Nathan C / El-Ashwah, Shaimaa / Cordoba, Raul / Hanakova, Michaela / Zambrotta, Giovanni / Sciumè, Mariarita / Booth, Stephen / Rodrigues, Raquel Nunes / Sacchi, Maria Vittoria / García-Poutón, Nicole / Martín-González, Juan-Alberto / Khostelidi, Sofya / Gräfe, Stefanie / Rahimli, Laman / Ammatuna, Emanuele / Busca, Alessandro / Corradini, Paolo / Hoenigl, Martin / Klimko, Nikolai / Koehler, Philipp / Pagliuca, Antonio / Passamonti, Francesco / Cornely, Oliver A / Pagano, Livio

    Haematologica

    2023  Volume 108, Issue 1, Page(s) 22–33

    Abstract: Patients with acute myeloid leukemia (AML) are at high risk of dying from coronavirus disease 2019 (COVID-19). The optimal management of AML patients with COVID-19 has not been established. Our multicenter study included 388 adult AML patients diagnosed ... ...

    Abstract Patients with acute myeloid leukemia (AML) are at high risk of dying from coronavirus disease 2019 (COVID-19). The optimal management of AML patients with COVID-19 has not been established. Our multicenter study included 388 adult AML patients diagnosed with COVID-19 between February 2020 and October 2021. The vast majority were receiving or had received AML treatment in the preceding 3 months. COVID-19 was severe in 41.2% and critical in 21.1% of cases. The chemotherapeutic schedule was modified in 174 patients (44.8%), delayed in 68 and permanently discontinued in 106. After a median follow-up of 325 days, 180 patients (46.4%) had died; death was attributed to COVID-19 (43.3%), AML (26.1%) or to a combination of both (26.7%), whereas in 3.9% of cases the reason was unknown. Active disease, older age, and treatment discontinuation were associated with death, whereas AML treatment delay was protective. Seventy-nine patients had a simultaneous AML and COVID-19 diagnosis, with better survival when AML treatment could be delayed (80%; P<0.001). Overall survival in patients with a diagnosis of COVID-19 between January 2020 and August 2020 was significantly lower than that in patients diagnosed between September 2020 and February 2021 and between March 2021 and September 2021 (39.8% vs. 60% vs. 61.9%, respectively; P=0.006). COVID-19 in AML patients was associated with a high mortality rate and modifications of therapeutic algorithms. The best approach to improve survival was to delay AML treatment, whenever possible.
    MeSH term(s) Humans ; Adult ; Follow-Up Studies ; COVID-19 Testing ; COVID-19 ; Leukemia, Myeloid, Acute/therapy ; Leukemia, Myeloid, Acute/drug therapy ; Hematology
    Language English
    Publishing date 2023-01-01
    Publishing country Italy
    Document type Multicenter Study ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2333-4
    ISSN 1592-8721 ; 0017-6567 ; 0390-6078
    ISSN (online) 1592-8721
    ISSN 0017-6567 ; 0390-6078
    DOI 10.3324/haematol.2022.280847
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  3. Article ; Online: Basophil-lineage commitment in acute promyelocytic leukemia predicts for severe bleeding after starting therapy.

    Matarraz, Sergio / Leoz, Pilar / Fernández, Carlos / Colado, Enrique / Chillón, María Carmen / Vidriales, María Belén / González, Marcos / Rivera, Daniel / Osuna, Carlos Salvador / Caballero-Velázquez, Teresa / Van Der Velden, Vincent / Jongen-Lavrencic, Mojca / Gutiérrez, Oliver / Bermejo, Ana Yeguas / Alonso, Luis García / García, Monique Bourgeois / De Ramón Sánchez, Cristina / García-Donas, Gloria / Mateo, Aránzazu García /
    Recio, Isabel / Sánchez-Real, Javier / Mayado, Andrea / Gutiérrez, María Laura / Bárcena, Paloma / Barrena, Susana / López, Antonio / Van Dongen, Jacques / Orfao, Alberto

    Modern pathology : an official journal of the United States and Canadian Academy of Pathology, Inc

    2018  Volume 31, Issue 8, Page(s) 1318–1331

    Abstract: Severe hemorrhagic events occur in a significant fraction of acute promyelocytic leukemia patients, either at presentation and/or early after starting therapy, leading to treatment failure and early deaths. However, identification of independent ... ...

    Abstract Severe hemorrhagic events occur in a significant fraction of acute promyelocytic leukemia patients, either at presentation and/or early after starting therapy, leading to treatment failure and early deaths. However, identification of independent predictors for high-risk of severe bleeding at diagnosis, remains a challenge. Here, we investigated the immunophenotype of bone marrow leukemic cells from 109 newly diagnosed acute promyelocytic leukemia patients, particularly focusing on the identification of basophil-related features, and their potential association with severe bleeding episodes and patient overall survival.From all phenotypes investigated on leukemic cells, expression of the CD203c and/or CD22 basophil-associated markers showed the strongest association with the occurrence and severity of bleeding (p ≤ 0.007); moreover, aberrant expression of CD7, coexpression of CD34
    MeSH term(s) Adolescent ; Adult ; Aged ; Aged, 80 and over ; Basophils/pathology ; Cell Lineage ; Child ; Child, Preschool ; Female ; Hemorrhage/etiology ; Humans ; Leukemia, Promyelocytic, Acute/complications ; Leukemia, Promyelocytic, Acute/pathology ; Male ; Middle Aged ; Phenotype ; Young Adult
    Language English
    Publishing date 2018-03-23
    Publishing country United States
    Document type Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 645073-8
    ISSN 1530-0285 ; 0893-3952
    ISSN (online) 1530-0285
    ISSN 0893-3952
    DOI 10.1038/s41379-018-0038-2
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

  4. Article ; Online: COVID-19 infection in adult patients with hematological malignancies: a European Hematology Association Survey (EPICOVIDEHA).

    Pagano, Livio / Salmanton-García, Jon / Marchesi, Francesco / Busca, Alessandro / Corradini, Paolo / Hoenigl, Martin / Klimko, Nikolai / Koehler, Philipp / Pagliuca, Antonio / Passamonti, Francesco / Verga, Luisa / Víšek, Benjamin / Ilhan, Osman / Nadali, Gianpaolo / Weinbergerová, Barbora / Córdoba-Mascuñano, Raúl / Marchetti, Monia / Collins, Graham P / Farina, Francesca /
    Cattaneo, Chiara / Cabirta, Alba / Gomes-Silva, Maria / Itri, Federico / van Doesum, Jaap / Ledoux, Marie-Pierre / Čerňan, Martin / Jakšić, Ozren / Duarte, Rafael F / Magliano, Gabriele / Omrani, Ali S / Fracchiolla, Nicola S / Kulasekararaj, Austin / Valković, Toni / Poulsen, Christian Bjørn / Machado, Marina / Glenthøj, Andreas / Stoma, Igor / Ráčil, Zdeněk / Piukovics, Klára / Navrátil, Milan / Emarah, Ziad / Sili, Uluhan / Maertens, Johan / Blennow, Ola / Bergantim, Rui / García-Vidal, Carolina / Prezioso, Lucia / Guidetti, Anna / Del Principe, Maria Ilaria / Popova, Marina / de Jonge, Nick / Ormazabal-Vélez, Irati / Fernández, Noemí / Falces-Romero, Iker / Cuccaro, Annarosa / Meers, Stef / Buquicchio, Caterina / Antić, Darko / Al-Khabori, Murtadha / García-Sanz, Ramón / Biernat, Monika M / Tisi, Maria Chiara / Sal, Ertan / Rahimli, Laman / Čolović, Natasa / Schönlein, Martin / Calbacho, Maria / Tascini, Carlo / Miranda-Castillo, Carolina / Khanna, Nina / Méndez, Gustavo-Adolfo / Petzer, Verena / Novák, Jan / Besson, Caroline / Duléry, Rémy / Lamure, Sylvain / Nucci, Marcio / Zambrotta, Giovanni / Žák, Pavel / Seval, Guldane Cengiz / Bonuomo, Valentina / Mayer, Jiří / López-García, Alberto / Sacchi, Maria Vittoria / Booth, Stephen / Ciceri, Fabio / Oberti, Margherita / Salvini, Marco / Izuzquiza, Macarena / Nunes-Rodrigues, Raquel / Ammatuna, Emanuele / Obr, Aleš / Herbrecht, Raoul / Núñez-Martín-Buitrago, Lucía / Mancini, Valentina / Shwaylia, Hawraa / Sciumè, Mariarita / Essame, Jenna / Nygaard, Marietta / Batinić, Josip / Gonzaga, Yung / Regalado-Artamendi, Isabel / Karlsson, Linda Katharina / Shapetska, Maryia / Hanakova, Michaela / El-Ashwah, Shaimaa / Borbényi, Zita / Çolak, Gökçe Melis / Nordlander, Anna / Dragonetti, Giulia / Maraglino, Alessio Maria Edoardo / Rinaldi, Amelia / De Ramón-Sánchez, Cristina / Cornely, Oliver A

    Journal of hematology & oncology

    2021  Volume 14, Issue 1, Page(s) 168

    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 ... ...

    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.
    MeSH term(s) Adult ; Aged ; Aged, 80 and over ; COVID-19/complications ; COVID-19/diagnosis ; COVID-19/epidemiology ; COVID-19/therapy ; Europe/epidemiology ; Female ; Hematologic Neoplasms/complications ; Hematologic Neoplasms/epidemiology ; Hematologic Neoplasms/therapy ; Hospitalization ; Humans ; Intensive Care Units ; Male ; Middle Aged ; Registries ; Risk Factors ; SARS-CoV-2/isolation & purification ; Young Adult
    Language English
    Publishing date 2021-10-14
    Publishing country England
    Document type Clinical Trial ; Journal Article ; Research Support, Non-U.S. Gov't
    ZDB-ID 2429631-4
    ISSN 1756-8722 ; 1756-8722
    ISSN (online) 1756-8722
    ISSN 1756-8722
    DOI 10.1186/s13045-021-01177-0
    Database MEDical Literature Analysis and Retrieval System OnLINE

    More links

    Kategorien

To top