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
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

1022901

Subventions

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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Auteurs

Dristhi Ragoonanan (D)

Department of Pediatrics, Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Saleh Bhar (S)

Texas Children's Hospital, Baylor College of Medicine, Houston, TX, United States.

Gopi Mohan (G)

Division of Pediatric Hematology-Oncology, Boston Children's Hospital, Boston, MA, United States.

Fernando Beltramo (F)

Children's Hospital Los Angeles, University of Southern California Keck School of Medicine, Los Angeles, CA, United States.

Sajad J Khazal (SJ)

Department of Pediatrics, Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Caitlin Hurley (C)

Department of Bone Marrow Transplantation and Cellular Therapy, St Jude Children's Research Hospital, Memphis, TN, United States.

Clark Andersen (C)

Department of Biostatistics, Division of Basic Sciences, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Steven Margossian (S)

Division of Pediatric Hematology-Oncology, Boston Children's Hospital, Boston, MA, United States.

Sattva S Neelapu (SS)

Department of Lymphoma and Myeloma, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Elizabeth Shpall (E)

Department of Stem Cell Transplantation and Cellular Therapy, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Cristina Gutierrez (C)

Department of Critical Care, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Priti Tewari (P)

Department of Pediatrics, Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Basirat Shoberu (B)

Department of Pediatrics, Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Aimee Talleur (A)

Department of Bone Marrow Transplantation and Cellular Therapy, St Jude Children's Research Hospital, Memphis, TN, United States.

David McCall (D)

Department of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Cesar Nunez (C)

Department of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Branko Cuglievan (B)

Department of Pediatrics, The University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Francesco Paolo Tambaro (FP)

Pediatric Stem Cell Transplantation and Cell Therapy Program, UOC SIT-TMO AORN Santobono-Pausilipon, Napoli, Italy.

Demetrios Petropoulos (D)

Department of Pediatrics, Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Hisham Abdel-Azim (H)

Division of Transplant and Cell Therapy, Loma Linda University Cancer Center, Loma Linda, CA, United States.

Kris M Mahadeo (KM)

Department of Pediatrics, Stem Cell Transplantation and Cellular Therapy, University of Texas MD Anderson Cancer Center, Houston, TX, United States.

Classifications MeSH