Cellular Therapy During COVID-19: Lessons Learned and Preparing for Subsequent Waves.
Adult
Aged
Allografts
Amyloidosis
/ therapy
Anemia, Aplastic
/ therapy
COVID-19
/ complications
Civil Defense
Cross Infection
/ epidemiology
Disease Progression
Evidence-Based Practice
/ organization & administration
Female
Hematopoietic Stem Cell Transplantation
/ statistics & numerical data
Humans
Immunotherapy, Adoptive
Infection Control
/ methods
Infectious Disease Transmission, Professional-to-Patient
Leukemia
/ mortality
Male
Middle Aged
Myelodysplastic-Myeloproliferative Diseases
/ mortality
Neoplasm, Residual
Neoplasms
/ mortality
New York City
/ epidemiology
Pandemics
Resource Allocation
SARS-CoV-2
Time-to-Treatment
/ statistics & numerical data
Transplantation, Autologous
Triage
/ organization & administration
Young Adult
COVID-19
Cellular therapy
Chimeric antigen receptor T cell therapy
Hematopoietic cell transplantation
Journal
Transplantation and cellular therapy
ISSN: 2666-6367
Titre abrégé: Transplant Cell Ther
Pays: United States
ID NLM: 101774629
Informations de publication
Date de publication:
05 2021
05 2021
Historique:
received:
24
12
2020
accepted:
07
02
2021
pubmed:
18
3
2021
medline:
14
5
2021
entrez:
17
3
2021
Statut:
ppublish
Résumé
An evidence-based triage plan for cellular therapy distribution is critical in the face of emerging constraints on healthcare resources. We evaluated the impact of treatment delays related to COVID-19 on patients scheduled to undergo hematopoietic cell transplantation (HCT) or chimeric antigen receptor T-cell (CAR-T) therapy at our center. Data were collected in real time between March 19 and May 11, 2020, for patients who were delayed to cellular therapy. We evaluated the proportion of delayed patients who ultimately received cellular therapy, reasons for not proceeding to cellular therapy, and changes in disease and health status during delay. A total of 85 patients were delayed, including 42 patients planned for autologous HCT, 36 patients planned for allogeneic HCT, and 7 patients planned for CAR-T therapy. Fifty-six of these patients (66%) since received planned therapy. Five patients died during the delay. The most common reason for not proceeding to autologous HCT was good disease control in patients with plasma cell dyscrasias (75%). The most common reason for not proceeding to allogeneic HCT was progression of disease (42%). All patients with acute leukemia who progressed had measurable residual disease (MRD) at the time of delay, whereas no patient without MRD at the time of delay progressed. Six patients (86%) ultimately received CAR-T therapy, including 3 patients who progressed during the delay. For patients with high-risk disease such as acute leukemia, and particularly those with MRD at the time of planned HCT, treatment delay can result in devastating outcomes and should be avoided if at all possible.
Identifiants
pubmed: 33728417
doi: 10.1016/j.jtct.2021.02.011
pii: S2666-6367(21)00677-1
pmc: PMC7952254
doi:
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Langues
eng
Sous-ensembles de citation
IM
Pagination
438.e1-438.e6Subventions
Organisme : NCI NIH HHS
ID : P01 CA023766
Pays : United States
Organisme : NCI NIH HHS
ID : P30 CA008748
Pays : United States
Informations de copyright
© 2021 The American Society for Transplantation and Cellular Therapy. Published by Elsevier Inc. All rights reserved.