A multicenter study of ICU resource utilization in pediatric, adolescent and young adult patients post CAR-T therapy.
AYA (adolescents and young adults)
CAR (chimeric antigen receptor) T-cell therapy
Immunotherapy
Resource utilisation
pediatric cancer
Journal
Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867
Informations de publication
Date de publication:
2022
2022
Historique:
received:
19
08
2022
accepted:
30
09
2022
entrez:
10
11
2022
pubmed:
11
11
2022
medline:
11
11
2022
Statut:
epublish
Résumé
Tisagenlecleucel is associated with remarkable outcomes in treating patients up to the age of 25 years with refractory B-cell acute lymphoblastic leukemia (ALL). Yet, due to unique and potentially life-threatening complications, access remains limited to higher-resource and certified centers. Reports of inequity and related disparities in care are emerging. In this multicenter study of ALL patients admitted for anti-leukemia therapy, who required pediatric intensive care (ICU) support (n = 205), patients receiving tisagenlecleucel (n = 39) were compared to those receiving conventional chemotherapy (n = 166). The median time to ICU transfer was 6 (0-43) versus 1 (0-116) days, respectively (p < 0.0001). There was no difference in the use of vasopressor, ionotropic, sedating, and/or paralytic agents between groups, but use of dexamethasone was higher among tisagenlecleucel patients. Patients receiving tisagenlecleucel were more likely to have cardiorespiratory toxicity (p = 0.0002), but there were no differences in diagnostic interventions between both groups and/or differences in ICU length of stay and/or overall hospital survival. Toxicities associated with tisagenlecleucel are generally reversible, and our findings suggest that resource utilization once admitted to the ICU may be similar among patients with ALL receiving tisagenlecleucel versus conventional chemotherapy. As centers consider improved access to care and the feasibility of tisagenlecleucel certification, our study may inform strategic planning.
Identifiants
pubmed: 36353531
doi: 10.3389/fonc.2022.1022901
pmc: PMC9638171
doi:
Types de publication
Journal Article
Langues
eng
Pagination
1022901Subventions
Organisme : NCI NIH HHS
ID : P30 CA016672
Pays : United States
Informations de copyright
Copyright © 2022 Ragoonanan, Bhar, Mohan, Beltramo, Khazal, Hurley, Andersen, Margossian, Neelapu, Shpall, Gutierrez, Tewari, Shoberu, Talleur, McCall, Nunez, Cuglievan, Tambaro, Petropoulos, Abdel-Azim and Mahadeo.
Déclaration de conflit d'intérêts
KM is the site PI for Atara Biotherapeutics, Jazz Pharma, Allovir, and BMS. CG has served in the Advisory Board for Legend Biotech & Janssen. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. The handling editor declared a past collaboration with author KM.
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