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Regional Injection of CAR-T Cells for the Treatment of Refractory and Recurrent Diffuse Large B Cell Lymphoma: A Case Report

BACKGROUND: Lymphoma is a common hematological malignancy with many subtypes and considerable heterogeneity. Traditional treatments include chemotherapy, radiotherapy, and surgery. Patients with relapsed, refractory or advanced stage lymphoma have a dismal prognosis. In recent years, chimeric antige...

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Autores principales: Wei, Yan-Hui, He, Yu-Zhuo, Lin, Xiao-Yan, Ren, Fu-Xian, Zhu, Hong-Bin, Cheng, Ying, Nan, Zhen, Liu, Zheng-Biao, Yu, Jing-Ya, Guo, Xue-Jun
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225683/
https://www.ncbi.nlm.nih.gov/pubmed/32457910
http://dx.doi.org/10.3389/fcell.2020.00333
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author Wei, Yan-Hui
He, Yu-Zhuo
Lin, Xiao-Yan
Ren, Fu-Xian
Zhu, Hong-Bin
Cheng, Ying
Nan, Zhen
Liu, Zheng-Biao
Yu, Jing-Ya
Guo, Xue-Jun
author_facet Wei, Yan-Hui
He, Yu-Zhuo
Lin, Xiao-Yan
Ren, Fu-Xian
Zhu, Hong-Bin
Cheng, Ying
Nan, Zhen
Liu, Zheng-Biao
Yu, Jing-Ya
Guo, Xue-Jun
author_sort Wei, Yan-Hui
collection PubMed
description BACKGROUND: Lymphoma is a common hematological malignancy with many subtypes and considerable heterogeneity. Traditional treatments include chemotherapy, radiotherapy, and surgery. Patients with relapsed, refractory or advanced stage lymphoma have a dismal prognosis. In recent years, chimeric antigen receptors (CARs) have been recognized as powerful tools that redirect antigen-specific T cells independent of human lymphocyte antigen (HLA) restriction and specifically kill tumor cells. Satisfactory results with CAR-based treatments have been achieved in relapsed/refractory B cell leukemia/lymphoma. Our center explored the strategy of subcutaneous injections combined with intravenous drip to overcome certain issues. CASE PRESENTATION: A patient with stage IV refractory and relapsed diffuse large B cell lymphoma was treated with regional and intravenous CAR-T cells. During the observation period, the temperature of the skin at the abdominal wall mass was slightly elevated, and tolerable pain in the injection area was reported. Imaging showed regional liquefactive necrosis. After the sequential administration of ibrutinib and venetoclax, the abdominal wall mass significantly decreased in size. CONCLUSION: The regional injection of CAR-T cells might be safe and feasible for the treatment of regional lesions in patients with refractory and relapsed advanced lymphoma.
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spelling pubmed-72256832020-05-25 Regional Injection of CAR-T Cells for the Treatment of Refractory and Recurrent Diffuse Large B Cell Lymphoma: A Case Report Wei, Yan-Hui He, Yu-Zhuo Lin, Xiao-Yan Ren, Fu-Xian Zhu, Hong-Bin Cheng, Ying Nan, Zhen Liu, Zheng-Biao Yu, Jing-Ya Guo, Xue-Jun Front Cell Dev Biol Cell and Developmental Biology BACKGROUND: Lymphoma is a common hematological malignancy with many subtypes and considerable heterogeneity. Traditional treatments include chemotherapy, radiotherapy, and surgery. Patients with relapsed, refractory or advanced stage lymphoma have a dismal prognosis. In recent years, chimeric antigen receptors (CARs) have been recognized as powerful tools that redirect antigen-specific T cells independent of human lymphocyte antigen (HLA) restriction and specifically kill tumor cells. Satisfactory results with CAR-based treatments have been achieved in relapsed/refractory B cell leukemia/lymphoma. Our center explored the strategy of subcutaneous injections combined with intravenous drip to overcome certain issues. CASE PRESENTATION: A patient with stage IV refractory and relapsed diffuse large B cell lymphoma was treated with regional and intravenous CAR-T cells. During the observation period, the temperature of the skin at the abdominal wall mass was slightly elevated, and tolerable pain in the injection area was reported. Imaging showed regional liquefactive necrosis. After the sequential administration of ibrutinib and venetoclax, the abdominal wall mass significantly decreased in size. CONCLUSION: The regional injection of CAR-T cells might be safe and feasible for the treatment of regional lesions in patients with refractory and relapsed advanced lymphoma. Frontiers Media S.A. 2020-05-08 /pmc/articles/PMC7225683/ /pubmed/32457910 http://dx.doi.org/10.3389/fcell.2020.00333 Text en Copyright © 2020 Wei, He, Lin, Ren, Zhu, Cheng, Nan, Liu, Yu and Guo. http://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 Cell and Developmental Biology
Wei, Yan-Hui
He, Yu-Zhuo
Lin, Xiao-Yan
Ren, Fu-Xian
Zhu, Hong-Bin
Cheng, Ying
Nan, Zhen
Liu, Zheng-Biao
Yu, Jing-Ya
Guo, Xue-Jun
Regional Injection of CAR-T Cells for the Treatment of Refractory and Recurrent Diffuse Large B Cell Lymphoma: A Case Report
title Regional Injection of CAR-T Cells for the Treatment of Refractory and Recurrent Diffuse Large B Cell Lymphoma: A Case Report
title_full Regional Injection of CAR-T Cells for the Treatment of Refractory and Recurrent Diffuse Large B Cell Lymphoma: A Case Report
title_fullStr Regional Injection of CAR-T Cells for the Treatment of Refractory and Recurrent Diffuse Large B Cell Lymphoma: A Case Report
title_full_unstemmed Regional Injection of CAR-T Cells for the Treatment of Refractory and Recurrent Diffuse Large B Cell Lymphoma: A Case Report
title_short Regional Injection of CAR-T Cells for the Treatment of Refractory and Recurrent Diffuse Large B Cell Lymphoma: A Case Report
title_sort regional injection of car-t cells for the treatment of refractory and recurrent diffuse large b cell lymphoma: a case report
topic Cell and Developmental Biology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7225683/
https://www.ncbi.nlm.nih.gov/pubmed/32457910
http://dx.doi.org/10.3389/fcell.2020.00333
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