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Case Report: Chimeric Antigen Receptor T Cells Induced Late Severe Cytokine Release Syndrome
BACKGROUND: Severe cytokine release syndrome (sCRS) has emerged as an adverse complication in the early period of chimeric antigen receptor T cell (CART) therapy, while whether sCRS occurs in the late period remains unknown. Here, we reported two patients with late sCRS. CASE PRESENTATION: Case 1 wa...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198280/ https://www.ncbi.nlm.nih.gov/pubmed/35719984 http://dx.doi.org/10.3389/fonc.2022.893928 |
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author | He, Jinping Xu, Na Zhou, Hongsheng Zhou, Ya Wu, Di Zhao, Ruochong Lin, Tong Xu, Ju Cao, Rui Li, Peng Liu, Qifa |
author_facet | He, Jinping Xu, Na Zhou, Hongsheng Zhou, Ya Wu, Di Zhao, Ruochong Lin, Tong Xu, Ju Cao, Rui Li, Peng Liu, Qifa |
author_sort | He, Jinping |
collection | PubMed |
description | BACKGROUND: Severe cytokine release syndrome (sCRS) has emerged as an adverse complication in the early period of chimeric antigen receptor T cell (CART) therapy, while whether sCRS occurs in the late period remains unknown. Here, we reported two patients with late sCRS. CASE PRESENTATION: Case 1 was a 34-year-old female with refractory Philadelphia chromosome-positive B cell acute lymphoblastic leukemia. She achieved complete remission (CR) but experienced grade III CRS and hemophagocytic lymphohistiocytosis (HLH) 41 days after CD19-targeted CART (CART19) cells and CD22-targeted CART (CART22) cells infusion. Ineffective to tocilizumab and HLH-94 protocol (dexamethasone and etoposide), she died of a cerebral hemorrhage on day 55 after CART therapy. Case 2 was a 38-year-old male with IgG kappa multiple myeloma. He received autologous BCMA-targeted CART (BCMA-CART) therapy 4 months after HLA–matched sibling (sister) donor transplantation and developed grade III CRS 163 days after CART administration, characterized by fever, hypotension, and skin lesions. Effective to methylprednisolone and tocilizumab, his clinical response persisted for over 6.0 months. CONCLUSION: Severe CRS could occur in the late period after CART therapy as re-expansion of CART cells possessed the potential risk for late sCRS. |
format | Online Article Text |
id | pubmed-9198280 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-91982802022-06-16 Case Report: Chimeric Antigen Receptor T Cells Induced Late Severe Cytokine Release Syndrome He, Jinping Xu, Na Zhou, Hongsheng Zhou, Ya Wu, Di Zhao, Ruochong Lin, Tong Xu, Ju Cao, Rui Li, Peng Liu, Qifa Front Oncol Oncology BACKGROUND: Severe cytokine release syndrome (sCRS) has emerged as an adverse complication in the early period of chimeric antigen receptor T cell (CART) therapy, while whether sCRS occurs in the late period remains unknown. Here, we reported two patients with late sCRS. CASE PRESENTATION: Case 1 was a 34-year-old female with refractory Philadelphia chromosome-positive B cell acute lymphoblastic leukemia. She achieved complete remission (CR) but experienced grade III CRS and hemophagocytic lymphohistiocytosis (HLH) 41 days after CD19-targeted CART (CART19) cells and CD22-targeted CART (CART22) cells infusion. Ineffective to tocilizumab and HLH-94 protocol (dexamethasone and etoposide), she died of a cerebral hemorrhage on day 55 after CART therapy. Case 2 was a 38-year-old male with IgG kappa multiple myeloma. He received autologous BCMA-targeted CART (BCMA-CART) therapy 4 months after HLA–matched sibling (sister) donor transplantation and developed grade III CRS 163 days after CART administration, characterized by fever, hypotension, and skin lesions. Effective to methylprednisolone and tocilizumab, his clinical response persisted for over 6.0 months. CONCLUSION: Severe CRS could occur in the late period after CART therapy as re-expansion of CART cells possessed the potential risk for late sCRS. Frontiers Media S.A. 2022-06-01 /pmc/articles/PMC9198280/ /pubmed/35719984 http://dx.doi.org/10.3389/fonc.2022.893928 Text en Copyright © 2022 He, Xu, Zhou, Zhou, Wu, Zhao, Lin, Xu, Cao, Li and Liu https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Oncology He, Jinping Xu, Na Zhou, Hongsheng Zhou, Ya Wu, Di Zhao, Ruochong Lin, Tong Xu, Ju Cao, Rui Li, Peng Liu, Qifa Case Report: Chimeric Antigen Receptor T Cells Induced Late Severe Cytokine Release Syndrome |
title | Case Report: Chimeric Antigen Receptor T Cells Induced Late Severe Cytokine Release Syndrome |
title_full | Case Report: Chimeric Antigen Receptor T Cells Induced Late Severe Cytokine Release Syndrome |
title_fullStr | Case Report: Chimeric Antigen Receptor T Cells Induced Late Severe Cytokine Release Syndrome |
title_full_unstemmed | Case Report: Chimeric Antigen Receptor T Cells Induced Late Severe Cytokine Release Syndrome |
title_short | Case Report: Chimeric Antigen Receptor T Cells Induced Late Severe Cytokine Release Syndrome |
title_sort | case report: chimeric antigen receptor t cells induced late severe cytokine release syndrome |
topic | Oncology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9198280/ https://www.ncbi.nlm.nih.gov/pubmed/35719984 http://dx.doi.org/10.3389/fonc.2022.893928 |
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