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Anti-CD19 CAR T as a feasible and safe therapy for refractory/relapsed mixed phenotype acute leukemia (MPAL) patients
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  • Xiangqun Li,
  • Kylann Chen,
  • Hailong Zhang,
  • Xian Zhang,
  • Junfang Yang ,
  • Jing Liu,
  • Jianwei Zheng,
  • Fei Dong,
  • Yongbo Zhu,
  • Jiao Yu,
  • Hailong Zhang,
  • Peihua Lu,
  • Bo Chen
Xiangqun Li
Kecellitics Biotech Company Ltd, Beijing, China

Corresponding Author:[email protected]

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Kylann Chen
University of Texas
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Hailong Zhang
Kecellitics Biotech Company Ltd, Beijing, China
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Xian Zhang
Hebei Yanda Lu Daopei Hospital
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Junfang Yang
Hebei Yanda Lu Daopei Hospital
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Jing Liu
Kecellitics Biotech Company Ltd, Beijing, China
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Jianwei Zheng
Kecellitics Biotech Company Ltd, Beijing, China
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Fei Dong
Kecellitics Biotech Company Ltd, Beijing, China
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Yongbo Zhu
Kecellitics Biotech Company Ltd, Beijing, China
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Jiao Yu
Kecellitics Biotech Company Ltd, Beijing, China
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Hailong Zhang
Kecellitics Biotech Company Ltd, Beijing, China
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Peihua Lu
Hebei Yanda Lu Daopei Hospital
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Bo Chen
Kecellitics Biotech Company Ltd, Beijing, China
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Abstract

Mixed phenotype acute leukemia (MPAL) is a relatively rare and heterogeneous group of diseases, which account for 2-5% of leukemia. So far, no optimal treatment regimens have been established for MPAL patients. CD19 chimeric antigen receptor T (CAR T) therapy have shown remarkable efficacy in B-ALL patients. In this study, 5 MPAL patients received CD19 CAR T cell infusion and 3 out of 5 patients (60%) achieved complete response (CR). 2 of 5 patients had only mild cytokine release syndrome (CRS). Neurotoxicity was not observed. Our data indicate that CD19 CAR T therapy is safe and effective for majority refractory/relapsed (r/r) MPAL patients.
19 Jan 2022Submission Checks Completed
19 Jan 2022Assigned to Editor
19 Jan 2022Submitted to Pediatric Blood & Cancer
20 Jan 2022Reviewer(s) Assigned
24 Jan 2022Review(s) Completed, Editorial Evaluation Pending
25 Jan 2022Editorial Decision: Revise Major
22 Feb 20221st Revision Received
22 Feb 2022Submission Checks Completed
22 Feb 2022Assigned to Editor
23 Feb 2022Review(s) Completed, Editorial Evaluation Pending
27 Feb 2022Editorial Decision: Accept