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CD19 and CD30 CAR T-Cell Immunotherapy for High-Risk Classical Hodgkin’s Lymphoma

Authors :
Alex H. Chang
Shaohui Liu
Zhen Li
Ruilei Li
Suwei Dong
Xun Lai
Qinghua Tan
Qiaofen Fu
Chunlei Ge
Baozhen Zeng
Yanlei Zhang
QingYin Meng
Jiyin Guo
Hong Yao
Liufang Zhao
Haiyan Ding
YuanBo Xue
Zhenhui Li
Jinyan Yang
Rongcheng Luo
Source :
Frontiers in Oncology, Vol 10 (2021), Frontiers in Oncology
Publication Year :
2021
Publisher :
Frontiers Media S.A., 2021.

Abstract

BackgroundIn clinical applications of CAR T-cell therapy, life-threatening adverse events including cytokine release syndrome and neurotoxicity can lead to treatment failure. Outcomes of patients treated with anti-CD30 CAR T- cell have been disappointing in relapsing/refractory (r/r) classical Hodgkin’s Lymphoma (cHL).MethodsIn order to understand the applicable population of multiple CAR T-cell therapy, we examined the expression of CD19, CD20, and CD30 by immunohistochemistry (IHC) in 38 paraffin-embedded specimens of cHL. In the past two years, we found only one patient with cHL who is eligible for combined anti-CD19 and CD30 CAR T-cell treatment. This patient’s baseline characteristics were prone to severe adverse events. We treated this patient with low doses and multiple infusions of anti-CD19 and CD30 CAR T-cell.ResultsThe positive expression of CD19+ + CD30+ in Reed-Sternberg (RS) cells is approximately 5.2% (2/38). The patient we treated with combined anti-CD19 and CD30 CAR T-cell did not experience severe adverse events related to CAR T-cell therapy and received long term progression-free survival (PFS).ConclusionFor high risk r/r cHL patients, low doses of CAR T-cell used over different days at different times might be safe and effective. More clinical trials are warranted for CD19 and CD30 CAR T-cell combination therapy.

Details

Language :
English
Volume :
10
Database :
OpenAIRE
Journal :
Frontiers in Oncology
Accession number :
edsair.doi.dedup.....9025a0d7c44ddf8cc57397f374987e31
Full Text :
https://doi.org/10.3389/fonc.2020.607362/full