open access

Vol 53, No 3 (2022)
Review article
Submitted: 2022-04-11
Accepted: 2022-04-15
Published online: 2022-05-25
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Outpatient CAR-T therapy

Dominik Dytfeld1, Lida Gil1
DOI: 10.5603/AHP.a2022.0020
·
Acta Haematol Pol 2022;53(3):180-182.
Affiliations
  1. Department of Hematology and Bone Marrow Transplantation, Poznan University of Medical Sciences, Szamarzewskiego 84, 60-569 Poznań, Poland

open access

Vol 53, No 3 (2022)
REVIEW ARTICLE
Submitted: 2022-04-11
Accepted: 2022-04-15
Published online: 2022-05-25

Abstract

Chimeric antigen receptor T (CAR-T) therapy has recently revolutionized the treatment of aggressive lymphomas and acute lymphoblastic leukemia, and will soon do the same for myeloma and other hematological malignancies. Due to the risk of potentially life-threatening complications such as cytokine release syndrome (CRS) and immune effector cell associated neurological syndrome (ICANS), patients have been hospitalized for the time when those symptoms may have occurred. However, due to improved prognostic factors, diagnostics and treatment of CRS and ICANS, it is possible that in the near future certain groups of patients will be treated with CAR as outpatients. That would allow broader access to CAR therapy, lowering overall costs and improving patient quality of life. Patient selection for outpatient CAR treatment is a topic that has been extensively discussed but, even based on the experience we already have, can already be effectively performed. CAR as an outpatient could be particularly useful for younger patients with a low tumor burden who have an educated caregiver and whose CAR center is logistically capable of providing outpatient care.

Abstract

Chimeric antigen receptor T (CAR-T) therapy has recently revolutionized the treatment of aggressive lymphomas and acute lymphoblastic leukemia, and will soon do the same for myeloma and other hematological malignancies. Due to the risk of potentially life-threatening complications such as cytokine release syndrome (CRS) and immune effector cell associated neurological syndrome (ICANS), patients have been hospitalized for the time when those symptoms may have occurred. However, due to improved prognostic factors, diagnostics and treatment of CRS and ICANS, it is possible that in the near future certain groups of patients will be treated with CAR as outpatients. That would allow broader access to CAR therapy, lowering overall costs and improving patient quality of life. Patient selection for outpatient CAR treatment is a topic that has been extensively discussed but, even based on the experience we already have, can already be effectively performed. CAR as an outpatient could be particularly useful for younger patients with a low tumor burden who have an educated caregiver and whose CAR center is logistically capable of providing outpatient care.

Get Citation

Keywords

CAR-T, outpatient, cellular therapy

About this article
Title

Outpatient CAR-T therapy

Journal

Acta Haematologica Polonica

Issue

Vol 53, No 3 (2022)

Article type

Review article

Pages

180-182

Published online

2022-05-25

Page views

2049

Article views/downloads

141

DOI

10.5603/AHP.a2022.0020

Bibliographic record

Acta Haematol Pol 2022;53(3):180-182.

Keywords

CAR-T
outpatient
cellular therapy

Authors

Dominik Dytfeld
Lida Gil

References (10)
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  4. Bachier CR, Godwin J, Andreadis C, et al. Outpatient treatment with lisocabtagene maraleucel (liso-cel) across a variety of clinical sites from three ongoing clinical studies in relapsed/refractory (R/R) large B-cell lymphoma (LBCL). J Clin Oncol . 2020; 38(15_suppl): 8037–8037.
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  8. Hayden PJ, Roddie C, Bader P, et al. Management of adults and children receiving CAR T-cell therapy: 2021 best practice recommendations of the European Society for Blood and Marrow Transplantation (EBMT) and the Joint Accreditation Committee of ISCT and EBMT (JACIE) and the European Haematology Association (EHA). Ann Oncol. 2022; 33(3): 259–275.
  9. Myers GD, Verneris MR, Goy A, et al. Perspectives on outpatient administration of CAR-T cell therapy in aggressive B-cell lymphoma and acute lymphoblastic leukemia. J Immunother Cancer. 2021; 9(4).
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