Frontiers in Oncology (Feb 2021)

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

  • YuanBo Xue,
  • YuanBo Xue,
  • Xun Lai,
  • RuiLei Li,
  • ChunLei Ge,
  • BaoZhen Zeng,
  • Zhen Li,
  • QiaoFen Fu,
  • LiuFang Zhao,
  • SuWei Dong,
  • JinYan Yang,
  • JiYin Guo,
  • QingYin Meng,
  • QingHua Tan,
  • ZhenHui Li,
  • HaiYan Ding,
  • YanLei Zhang,
  • ShaoHui Liu,
  • Alex H. Chang,
  • Hong Yao,
  • RongCheng Luo

DOI
https://doi.org/10.3389/fonc.2020.607362
Journal volume & issue
Vol. 10

Abstract

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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.

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