Outcomes in patients treated with chimeric ...
Document type :
Article dans une revue scientifique: Article original
PMID :
Permalink :
Title :
Outcomes in patients treated with chimeric antigen receptor t-cell therapy who were admitted to intensive care (carttas): an international, multicentre, observational cohort study
Author(s) :
Azoulay, Elie [Auteur]
Hopital Saint-Louis [AP-HP] [AP-HP]
Castro, Pedro [Auteur]
Maamar, Adel [Auteur]
Université de Rennes - Faculté de Médecine [UR Médecine]
Service des maladies infectieuses et réanimation médicale [Rennes] = Infectious Disease and Intensive Care [Rennes]
Centre d'Investigation Clinique [Rennes] [CIC]
Metaxa, Victoria [Auteur]
De Moraes, Alice Gallo [Auteur]
Voigt, Louis [Auteur]
Wallet, Florent [Auteur]
Centre Hospitalier Lyon Sud [CHU - HCL] [CHLS]
Service d'anesthésie-réanimation [Centre Hospitalier Lyon Sud - HCL]
Klouche, Kada [Auteur]
Département d'Anesthésie-Réanimation [Gui de Chauliac - CHU Montpellier]
Hôpital Lapeyronie [CHU Montpellier]
Picard, Muriel [Auteur]
Institut Universitaire du Cancer de Toulouse - Oncopole [IUCT Oncopole - UMR 1037]
Pôle Anesthésie Réanimation [CHU de Toulouse]
Moreau, Anne-Sophie [Auteur]
Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille]
Van De Louw, Andry [Auteur]
Seguin, Amelie [Auteur]
Centre Hospitalier Universitaire de Nantes = Nantes University Hospital [CHU Nantes]
Mokart, Djamel [Auteur]
Institut Paoli-Calmettes [IPC]
Chawla, Sanjay [Auteur]
Leroy, Julien [Auteur]
Hopital Saint-Louis [AP-HP] [AP-HP]
Boll, Boris [Auteur]
Issa, Nahema [Auteur]
Université de Bordeaux [UB]
Hôpital Saint-André
Levy, Bruno [Auteur]
Défaillance Cardiovasculaire Aiguë et Chronique [DCAC]
Centre Hospitalier Régional Universitaire de Nancy [CHRU Nancy]
Hemelaar, Pleun [Auteur]
Fernandez, Sara [Auteur]
Munshi, Laveena [Auteur]
Bauer, Philippe [Auteur]
Schellongowski, Peter [Auteur]
Joannidis, Michael [Auteur]
Moreno-Gonzalez, Gabriel [Auteur]
Galstian, Gennadii [Auteur]
Darmon, Michael [Auteur]
Service d'Anesthésie-Réanimation [AP-HP Hôpitaux Saint-Louis Lariboisière]
Hopital Saint-Louis [AP-HP] [AP-HP]
Valade, Sandrine [Auteur]
Hopital Saint-Louis [AP-HP] [AP-HP]
Hopital Saint-Louis [AP-HP] [AP-HP]
Castro, Pedro [Auteur]
Maamar, Adel [Auteur]
Université de Rennes - Faculté de Médecine [UR Médecine]
Service des maladies infectieuses et réanimation médicale [Rennes] = Infectious Disease and Intensive Care [Rennes]
Centre d'Investigation Clinique [Rennes] [CIC]
Metaxa, Victoria [Auteur]
De Moraes, Alice Gallo [Auteur]
Voigt, Louis [Auteur]
Wallet, Florent [Auteur]
Centre Hospitalier Lyon Sud [CHU - HCL] [CHLS]
Service d'anesthésie-réanimation [Centre Hospitalier Lyon Sud - HCL]
Klouche, Kada [Auteur]
Département d'Anesthésie-Réanimation [Gui de Chauliac - CHU Montpellier]
Hôpital Lapeyronie [CHU Montpellier]
Picard, Muriel [Auteur]
Institut Universitaire du Cancer de Toulouse - Oncopole [IUCT Oncopole - UMR 1037]
Pôle Anesthésie Réanimation [CHU de Toulouse]
Moreau, Anne-Sophie [Auteur]
Centre Hospitalier Régional Universitaire [CHU Lille] [CHRU Lille]
Van De Louw, Andry [Auteur]
Seguin, Amelie [Auteur]
Centre Hospitalier Universitaire de Nantes = Nantes University Hospital [CHU Nantes]
Mokart, Djamel [Auteur]
Institut Paoli-Calmettes [IPC]
Chawla, Sanjay [Auteur]
Leroy, Julien [Auteur]
Hopital Saint-Louis [AP-HP] [AP-HP]
Boll, Boris [Auteur]
Issa, Nahema [Auteur]
Université de Bordeaux [UB]
Hôpital Saint-André
Levy, Bruno [Auteur]
Défaillance Cardiovasculaire Aiguë et Chronique [DCAC]
Centre Hospitalier Régional Universitaire de Nancy [CHRU Nancy]
Hemelaar, Pleun [Auteur]
Fernandez, Sara [Auteur]
Munshi, Laveena [Auteur]
Bauer, Philippe [Auteur]
Schellongowski, Peter [Auteur]
Joannidis, Michael [Auteur]
Moreno-Gonzalez, Gabriel [Auteur]
Galstian, Gennadii [Auteur]
Darmon, Michael [Auteur]
Service d'Anesthésie-Réanimation [AP-HP Hôpitaux Saint-Louis Lariboisière]
Hopital Saint-Louis [AP-HP] [AP-HP]
Valade, Sandrine [Auteur]
Hopital Saint-Louis [AP-HP] [AP-HP]
Journal title :
The Lancet Haematology
Abbreviated title :
Lancet Haematol
Volume number :
8
Pages :
e355-e364
Publication date :
2021-05-01
ISSN :
2352-3026
HAL domain(s) :
Sciences du Vivant [q-bio]
English abstract : [en]
BACKGROUND: Chimeric antigen receptor (CAR) T-cell therapy can induce side-effects such as cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome (ICANS), which often require intensive care ...
Show more >BACKGROUND: Chimeric antigen receptor (CAR) T-cell therapy can induce side-effects such as cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome (ICANS), which often require intensive care unit admission. The aim of this study was to describe management of critically ill CAR T-cell recipients in intensive care. METHODS: This international, multicentre, observational cohort study was done in 21 intensive care units in France, Spain, the USA, the UK, Russia, Canada, Germany, and Austria. Eligible patients were aged 18 years or older; had received CAR T-cell therapy in the past 30 days; and had been admitted to intensive care for any reason. Investigators retrospectively included patients admitted between Feb 1, 2018, and Feb 1, 2019, and prospectively included patients admitted between March 1, 2019, and Feb 1, 2020. Demographic, clinical, laboratory, treatment, and outcome data were extracted from medical records. The primary endpoint was 90-day mortality. Factors associated with mortality were identified using a Cox proportional hazard model. RESULTS: 942 patients received CAR T-cell therapy, of whom 258 (27%) required admission to intensive care and 241 (26%) were included in the analysis. Admission to intensive care was needed within median 4·5 days (IQR 2·0-7·0) of CAR T-cell infusion. 90-day mortality was 22·4% (95% CI 17·1-27·7; 54 deaths). At initial evaluation on admission, isolated cytokine release syndrome was identified in 101 patients (42%), cytokine release syndrome and ICANS in 93 (39%), and isolated ICANS in seven (3%) patients. Grade 3-4 cytokine release syndrome within 1 day of admission to intensive care was found in 50 (25%) of 200 patients and grade 3-4 ICANS in 38 (35%) of 108 patients. Bacterial infection developed in 30 (12%) patients. Life-saving treatments were used in 75 (31%) patients within 24 h of admission to intensive care, primarily vasoactive drugs in 65 (27%) patients. Factors independently associated with 90-day mortality by multivariable analysis were frailty (hazard ratio 2·51 [95% CI 1·37-4·57]), bacterial infection (2·12 [1·11-4·08]), and lifesaving therapy within 24 h of admission (1·80 [1·05-3·10]). CONCLUSIONS: Critical care management is an integral part of CAR T-cell therapy and should be standardised. Studies to improve infection prevention and treatment in these high-risk patients are warranted. BACKGROUND: Groupe de Recherche Respiratoire en Réanimation Onco-Hématologique.Show less >
Show more >BACKGROUND: Chimeric antigen receptor (CAR) T-cell therapy can induce side-effects such as cytokine release syndrome and immune effector cell-associated neurotoxicity syndrome (ICANS), which often require intensive care unit admission. The aim of this study was to describe management of critically ill CAR T-cell recipients in intensive care. METHODS: This international, multicentre, observational cohort study was done in 21 intensive care units in France, Spain, the USA, the UK, Russia, Canada, Germany, and Austria. Eligible patients were aged 18 years or older; had received CAR T-cell therapy in the past 30 days; and had been admitted to intensive care for any reason. Investigators retrospectively included patients admitted between Feb 1, 2018, and Feb 1, 2019, and prospectively included patients admitted between March 1, 2019, and Feb 1, 2020. Demographic, clinical, laboratory, treatment, and outcome data were extracted from medical records. The primary endpoint was 90-day mortality. Factors associated with mortality were identified using a Cox proportional hazard model. RESULTS: 942 patients received CAR T-cell therapy, of whom 258 (27%) required admission to intensive care and 241 (26%) were included in the analysis. Admission to intensive care was needed within median 4·5 days (IQR 2·0-7·0) of CAR T-cell infusion. 90-day mortality was 22·4% (95% CI 17·1-27·7; 54 deaths). At initial evaluation on admission, isolated cytokine release syndrome was identified in 101 patients (42%), cytokine release syndrome and ICANS in 93 (39%), and isolated ICANS in seven (3%) patients. Grade 3-4 cytokine release syndrome within 1 day of admission to intensive care was found in 50 (25%) of 200 patients and grade 3-4 ICANS in 38 (35%) of 108 patients. Bacterial infection developed in 30 (12%) patients. Life-saving treatments were used in 75 (31%) patients within 24 h of admission to intensive care, primarily vasoactive drugs in 65 (27%) patients. Factors independently associated with 90-day mortality by multivariable analysis were frailty (hazard ratio 2·51 [95% CI 1·37-4·57]), bacterial infection (2·12 [1·11-4·08]), and lifesaving therapy within 24 h of admission (1·80 [1·05-3·10]). CONCLUSIONS: Critical care management is an integral part of CAR T-cell therapy and should be standardised. Studies to improve infection prevention and treatment in these high-risk patients are warranted. BACKGROUND: Groupe de Recherche Respiratoire en Réanimation Onco-Hématologique.Show less >
Language :
Anglais
Audience :
Internationale
Popular science :
Non
Administrative institution(s) :
CHU Lille
Inserm
Université de Lille
Inserm
Université de Lille
Submission date :
2021-07-06T12:46:38Z
2024-03-05T09:48:58Z
2024-03-05T09:48:58Z
Files
- document
- Open access
- Access the document