Improved efficacy with early tocilizumab in the prophylaxis and treatment of cytokine release syndrome of chimeric antigen receptor T cell (CAR-T) therapy for diffuse large B-cell lymphoma than acute lymphoblastic leukemia

Background: Tocilizumab is a well-practiced strategy to manage cytokine release syndrome (CRS) after chimeric antigen receptor T cell (CAR-T) therapy. However, varied efficiency in CRS mitigation by tocilizumab has been reported to highlight affecting variables such as tumor types and timing of the...

Full description

Bibliographic Details
Main Authors: Chengxin Luan, Haixia Wang, Junjie Zhou, Zhangbiao Long, Xin Chen, Xiaowen Chen, Jing Ni, Zhengqi Huang, Ruixiang Xia, Jian Ge
Format: Article
Language:English
Published: KeAi Communications Co., Ltd. 2023-09-01
Series:Biomedical Technology
Subjects:
Online Access:http://www.sciencedirect.com/science/article/pii/S2949723X23000028
_version_ 1797736804239015936
author Chengxin Luan
Haixia Wang
Junjie Zhou
Zhangbiao Long
Xin Chen
Xiaowen Chen
Jing Ni
Zhengqi Huang
Ruixiang Xia
Jian Ge
author_facet Chengxin Luan
Haixia Wang
Junjie Zhou
Zhangbiao Long
Xin Chen
Xiaowen Chen
Jing Ni
Zhengqi Huang
Ruixiang Xia
Jian Ge
author_sort Chengxin Luan
collection DOAJ
description Background: Tocilizumab is a well-practiced strategy to manage cytokine release syndrome (CRS) after chimeric antigen receptor T cell (CAR-T) therapy. However, varied efficiency in CRS mitigation by tocilizumab has been reported to highlight affecting variables such as tumor types and timing of the administration. Objective: The objective of this study is to identify different curative effect between diffuse large B-cell lymphoma (DLBCL) and acute lymphoblastic leukemia (ALL) by early use of tocilizumab for prophylaxis and treatment of CRS. Methods: By retrospectively summarizing our institution's experience with a CAR-T clinical trial targeting CD19, 11 cases were analyzed: 5 DLBCL, and 6 ALL. The two groups were compared with patient characteristics, CRS information and clinical outcomes. 3 patients were pretreated with tocilizumab for prophylaxis and the rest were treated with tocilizumab at CRS diagnosis. Results: CRS occurred in 81.8% of patients (9/11), grade 3 or higher occurred in 55.6% of the CRS patients (5/9). The two group were similar in patient characteristics, CAR-T and CRS profile. However, tocilizumab produced much better efficacy against CRS in DLBCL group compared with ALL group (80% versus 16.7%, P ​= ​0.08). Conclusions: Despite the statistical was non-significant, possibly due to small case pool and bias was unavoidable, our analysis suggested that early use of tocilizumab was more effective for DLBCL than ALL in the prophylaxis and treatment of CRS. A treatment algorithm for management of CRS with regard to DLBCL and ALL is proposed, which may extend to other local or systemic malignancies and warrant further investigation.
first_indexed 2024-03-12T13:19:14Z
format Article
id doaj.art-318c40d0a0ac4162bd72a6440006f514
institution Directory Open Access Journal
issn 2949-723X
language English
last_indexed 2024-03-12T13:19:14Z
publishDate 2023-09-01
publisher KeAi Communications Co., Ltd.
record_format Article
series Biomedical Technology
spelling doaj.art-318c40d0a0ac4162bd72a6440006f5142023-08-26T04:44:31ZengKeAi Communications Co., Ltd.Biomedical Technology2949-723X2023-09-0135965Improved efficacy with early tocilizumab in the prophylaxis and treatment of cytokine release syndrome of chimeric antigen receptor T cell (CAR-T) therapy for diffuse large B-cell lymphoma than acute lymphoblastic leukemiaChengxin Luan0Haixia Wang1Junjie Zhou2Zhangbiao Long3Xin Chen4Xiaowen Chen5Jing Ni6Zhengqi Huang7Ruixiang Xia8Jian Ge9Department of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaDepartment of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaDepartment of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaDepartment of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaDepartment of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaDepartment of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaDepartment of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaDepartment of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaDepartment of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaCorresponding author. Anhui Medical University, No.218, Jixi Road, Shushan District, Hefei, 230022, China.; Department of Hematology, The First Affiliated Hospital of Anhui Medical University, Hefei, ChinaBackground: Tocilizumab is a well-practiced strategy to manage cytokine release syndrome (CRS) after chimeric antigen receptor T cell (CAR-T) therapy. However, varied efficiency in CRS mitigation by tocilizumab has been reported to highlight affecting variables such as tumor types and timing of the administration. Objective: The objective of this study is to identify different curative effect between diffuse large B-cell lymphoma (DLBCL) and acute lymphoblastic leukemia (ALL) by early use of tocilizumab for prophylaxis and treatment of CRS. Methods: By retrospectively summarizing our institution's experience with a CAR-T clinical trial targeting CD19, 11 cases were analyzed: 5 DLBCL, and 6 ALL. The two groups were compared with patient characteristics, CRS information and clinical outcomes. 3 patients were pretreated with tocilizumab for prophylaxis and the rest were treated with tocilizumab at CRS diagnosis. Results: CRS occurred in 81.8% of patients (9/11), grade 3 or higher occurred in 55.6% of the CRS patients (5/9). The two group were similar in patient characteristics, CAR-T and CRS profile. However, tocilizumab produced much better efficacy against CRS in DLBCL group compared with ALL group (80% versus 16.7%, P ​= ​0.08). Conclusions: Despite the statistical was non-significant, possibly due to small case pool and bias was unavoidable, our analysis suggested that early use of tocilizumab was more effective for DLBCL than ALL in the prophylaxis and treatment of CRS. A treatment algorithm for management of CRS with regard to DLBCL and ALL is proposed, which may extend to other local or systemic malignancies and warrant further investigation.http://www.sciencedirect.com/science/article/pii/S2949723X23000028Chimeric antigen receptor T cell therapyCytokine release syndromeTocilizumabDiffuse large B-cell lymphoma (DLBCL)Acute lymphoblastic leukemia (ALL)
spellingShingle Chengxin Luan
Haixia Wang
Junjie Zhou
Zhangbiao Long
Xin Chen
Xiaowen Chen
Jing Ni
Zhengqi Huang
Ruixiang Xia
Jian Ge
Improved efficacy with early tocilizumab in the prophylaxis and treatment of cytokine release syndrome of chimeric antigen receptor T cell (CAR-T) therapy for diffuse large B-cell lymphoma than acute lymphoblastic leukemia
Biomedical Technology
Chimeric antigen receptor T cell therapy
Cytokine release syndrome
Tocilizumab
Diffuse large B-cell lymphoma (DLBCL)
Acute lymphoblastic leukemia (ALL)
title Improved efficacy with early tocilizumab in the prophylaxis and treatment of cytokine release syndrome of chimeric antigen receptor T cell (CAR-T) therapy for diffuse large B-cell lymphoma than acute lymphoblastic leukemia
title_full Improved efficacy with early tocilizumab in the prophylaxis and treatment of cytokine release syndrome of chimeric antigen receptor T cell (CAR-T) therapy for diffuse large B-cell lymphoma than acute lymphoblastic leukemia
title_fullStr Improved efficacy with early tocilizumab in the prophylaxis and treatment of cytokine release syndrome of chimeric antigen receptor T cell (CAR-T) therapy for diffuse large B-cell lymphoma than acute lymphoblastic leukemia
title_full_unstemmed Improved efficacy with early tocilizumab in the prophylaxis and treatment of cytokine release syndrome of chimeric antigen receptor T cell (CAR-T) therapy for diffuse large B-cell lymphoma than acute lymphoblastic leukemia
title_short Improved efficacy with early tocilizumab in the prophylaxis and treatment of cytokine release syndrome of chimeric antigen receptor T cell (CAR-T) therapy for diffuse large B-cell lymphoma than acute lymphoblastic leukemia
title_sort improved efficacy with early tocilizumab in the prophylaxis and treatment of cytokine release syndrome of chimeric antigen receptor t cell car t therapy for diffuse large b cell lymphoma than acute lymphoblastic leukemia
topic Chimeric antigen receptor T cell therapy
Cytokine release syndrome
Tocilizumab
Diffuse large B-cell lymphoma (DLBCL)
Acute lymphoblastic leukemia (ALL)
url http://www.sciencedirect.com/science/article/pii/S2949723X23000028
work_keys_str_mv AT chengxinluan improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia
AT haixiawang improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia
AT junjiezhou improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia
AT zhangbiaolong improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia
AT xinchen improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia
AT xiaowenchen improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia
AT jingni improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia
AT zhengqihuang improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia
AT ruixiangxia improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia
AT jiange improvedefficacywithearlytocilizumabintheprophylaxisandtreatmentofcytokinereleasesyndromeofchimericantigenreceptortcellcarttherapyfordiffuselargebcelllymphomathanacutelymphoblasticleukemia