Extracorporeal Membrane Oxygenation Candidacy in Pediatric Patients Treated With Hematopoietic Stem Cell Transplant and Chimeric Antigen Receptor T-Cell Therapy: An International Survey.

chimeric antigen receptor T-cell (CAR-T) therapy extracorporeal life support (ECLS) extracorporeal membrane oxyenation hematopoeietic cell transplant onco-critical care pediatric critical care pediatric oncology

Journal

Frontiers in oncology
ISSN: 2234-943X
Titre abrégé: Front Oncol
Pays: Switzerland
ID NLM: 101568867

Informations de publication

Date de publication:
2021
Historique:
received: 19 10 2021
accepted: 06 12 2021
entrez: 10 1 2022
pubmed: 11 1 2022
medline: 11 1 2022
Statut: epublish

Résumé

Pediatric patients who undergo hematopoietic cell transplant (HCT) or chimeric antigen receptor T-cell (CAR-T) therapy are at high risk for complications leading to organ failure and the need for critical care resources. Extracorporeal membrane oxygenation (ECMO) is a supportive modality that is used for cardiac and respiratory failure refractory to conventional therapies. While the use of ECMO is increasing for patients who receive HCT, candidacy for these patients remains controversial. We therefore surveyed pediatric critical care and HCT providers across North America and Europe to evaluate current provider opinions and decision-making and institutional practices regarding ECMO use for patients treated with HCT or CAR-T. An electronic twenty-eight question survey was distributed to pediatric critical care and HCT providers practicing in North America (United States and Canada) and Europe through the Pediatric Acute Lung Injury and Sepsis Investigators (PALISI) Network and individual emails. Responses to the survey were recorded in a REDCap Two-hundred and ten participants completed the survey. Of these, 159 (76%) identified themselves as pediatric critical care physicians and 47 (22%) as pediatric HCT physicians or oncologists. The majority (99.5%) of survey respondents stated that they would consider patients treated with HCT or CAR-T therapy as candidates for ECMO support. However, pediatric critical care physicians identified more absolute and relative contraindications for ECMO than non-pediatric critical care physicians. While only 0.5% of respondents reported that they consider HCT as an absolute contraindication for ECMO, 6% of respondents stated that ECMO is contraindicated in HCT patients within their institution and only 23% have an institutional protocol or policy to guide the evaluation for ECMO candidacy of these patients. Almost half (49.1%) of respondents would accept a survival to hospital discharge of 20-30% for pediatric HCT patients requiring ECMO as adequate. ECMO use for pediatric patients treated with HCT and CAR-T therapy is generally acceptable amongst physicians. However, there are differences in the evaluation and decision-making regarding ECMO candidacy amongst providers across medical specialties and institutions. Therefore, multidisciplinary collaboration is an essential component in establishing practice guidelines and advancing ECMO outcomes for these patients.

Identifiants

pubmed: 35004323
doi: 10.3389/fonc.2021.798236
pmc: PMC8727600
doi:

Types de publication

Journal Article

Langues

eng

Pagination

798236

Informations de copyright

Copyright © 2021 Ghafoor, Fan, Di Nardo, Talleur, Saini, Potera, Lehmann, Annich, Wang, McArthur, Sandhu and the Pediatric Acute Lung Injury and Sepsis Investigator (PALISI) Network.

Déclaration de conflit d'intérêts

The 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 reviewer NJS declared a shared affiliation with one of the authors JM, to the handling editor at the time of review.

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Auteurs

Saad Ghafoor (S)

Department of Pediatric Medicine, Division of Critical Care, St. Jude Children's Research Hospital, Memphis, TN, United States.

Kimberly Fan (K)

Department of Pediatric Medicine, Division of Critical Care, St. Jude Children's Research Hospital, Memphis, TN, United States.
Division of Pediatric Critical Care, University of Tennessee (IT) Health Science Center, Memphis, TN, United States.

Matteo Di Nardo (M)

Pediatric Intensive Care Unit, Bambino Gesù Children's Hospital, Istituto di Ricovero e Cura a Carattere Scientifico (IRCCS), Rome, Italy.

Aimee C Talleur (AC)

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

Arun Saini (A)

Division of Pediatric Critical Care, Texas Children's Hospital and Baylor College of Medicine, Houston, TX, United States.

Renee M Potera (RM)

Division of Pediatric Critical Care, University of Tennessee (UT) Southwestern Medical Center, Dallas, TX, United States.

Leslie Lehmann (L)

Pediatric Hematology-Oncology, Dana Farber Boston Children's Cancer and Blood Disorder Center, Boston, MA, United States.

Gail Annich (G)

Department of Critical Care Medicine, University of Toronto/The Hospital for Sick Children, Toronto, ON, Canada.

Fang Wang (F)

Department of Biostatistics, St. Jude Children's Research Hospital, Memphis, TN, United States.

Jennifer McArthur (J)

Department of Pediatric Medicine, Division of Critical Care, St. Jude Children's Research Hospital, Memphis, TN, United States.
Division of Pediatric Critical Care, Medical College of Wisconsin, Milwaukee, WI, United States.

Hitesh Sandhu (H)

Division of Pediatric Critical Care, University of Tennessee (IT) Health Science Center, Memphis, TN, United States.

Classifications MeSH