Impact of SARS-CoV-2 vaccination and monoclonal antibodies on outcome post-CD19-directed CAR T-cell therapy: an EPICOVIDEHA survey
Jazyk angličtina Země Spojené státy americké Médium print
Typ dokumentu multicentrická studie, časopisecké články
PubMed
37058479
PubMed Central
PMC10112941
DOI
10.1182/bloodadvances.2022009578
PII: 495340
Knihovny.cz E-zdroje
- MeSH
- adaptorové proteiny signální transdukční MeSH
- antigeny CD19 MeSH
- COVID-19 * terapie MeSH
- imunoterapie adoptivní MeSH
- lidé MeSH
- monoklonální protilátky MeSH
- retrospektivní studie MeSH
- SARS-CoV-2 MeSH
- testování na COVID-19 MeSH
- vakcinace MeSH
- vakcíny proti COVID-19 MeSH
- Check Tag
- lidé MeSH
- Publikační typ
- časopisecké články MeSH
- multicentrická studie MeSH
- Názvy látek
- adaptorové proteiny signální transdukční MeSH
- antigeny CD19 MeSH
- monoklonální protilátky MeSH
- vakcíny proti COVID-19 MeSH
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.
Aristotle University of Thessaloniki Thessaloniki Greece
Azienda Ospedaliera Nazionale SS Antonio e Biagio e Cesare Arrigo Alessandria Italy
Centre Hospitalier d'Argenteuil Argenteuil France
Centre Hospitalier de Versailles Le Chesnay France
Centro de Investigación Biomédica en Red Instituto de Salud Carlos 3 Madrid Spain
Complejo Hospitalario de Navarra Iruña Pamplona Spain
Departament de Medicina Universitat Autònoma de Barcelona Bellaterra Spain
Department of Hematology and Oncology Medical University of Innsbruck Innsbruck Austria
Department of Hematology UZ Leuven Leuven Belgium
Department of Infectious Diseases Karolinska University Hospital Stockholm Sweden
Department of Microbiology Immunology and Transplantation KU Leuven Leuven Belgium
Department of Nephrology and Infectious Diseases AZ Sint Jan Brugge Oostende AV Brugge Belgium
Department of Oncohematology Comenius University and National Cancer Institute Bratislava Slovakia
Faculty of Medicine University Medical Center Hamburg Eppendorf Hamburg Germany
Fundacion Jimenez Diaz University Hospital Health Research Institute IIS FJD Madrid Spain
German Centre for Infection Research Partner Site Bonn Cologne Cologne Germany
Hematology and Stem Cell Transplant Unit IRCCS Regina Elena National Cancer Institute Rome Italy
Hematology Department Hospital Universitario de Salamanca Salamanca Spain
Hematology Unit Fondazione Policlinico Universitario Agostino Gemelli IRCCS Rome Italy
Hospital Universitario 12 de Octubre Madrid Spain
Hospital Universitario Infanta Leonor Madrid Spain
Hospital Universitario Marqués de Valdecilla Santander Spain
Hospital Univesitario Virgen del Rocío Seville Spain
IRCCS Ospedale San Raffaele Milan Italy
Istituto Oncologico della Svizzera Italiana Bellinzona Switzerland
King's College Hospital London United Kingdom
La Paz University Hospital Madrid Spain
Ospedale San Bortolo Vicenza Italy
Portuguese Institute of Oncology Lisbon Portugal
School of Medicine University of Zagreb Zagreb Croatia
Service d'Hematologie Oncologie Hopital St Louis Assistance Publique Hopitaux de Paris Paris France
Universite de Paris Diderot Paris France
University Hospital Centre Zagreb Zagreb Croatia
University Medical Center Groningen Groningen The Netherlands
University of Milan and Fondazione IRCCS Istituto Nazionale Dei Tumori Milan Italy
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ClinicalTrials.gov
NCT04733729