Influence of patient characteristics on chimeric antigen receptor T cell therapy in B-cell acute lymphoblastic leukemia

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作者
Furun An
Huiping Wang
Zhenyun Liu
Fan Wu
Jiakui Zhang
Qianshan Tao
Yingwei Li
Yuanyuan Shen
Yanjie Ruan
Qing Zhang
Ying Pan
Weiwei Zhu
Hui Qin
Yansheng Wang
Yongling Fu
Zhenqing Feng
Zhimin Zhai
机构
[1] Hematology Department,
[2] the Second Hospital of Anhui Medical University (SHAMU),undefined
[3] Hematologic Diseases Research Center of Anhui Medical University,undefined
[4] Sinobioway Cell Therapy Co.,undefined
[5] Ltd.,undefined
[6] Key Laboratory of Antibody Technique of National Health Commission,undefined
[7] Nanjing Medical University,undefined
[8] Jiangsu Key Lab. of Cancer Biomarkers,undefined
[9] Prevention and Treatment,undefined
[10] Collaborative Innovation Center for Cancer Personalized Medicine,undefined
[11] Nanjing Medical University,undefined
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摘要
CD19-specific chimeric antigen receptor T cell (CD19 CAR T) therapy has shown high remission rates in patients with refractory/relapsed B-cell acute lymphoblastic leukemia (r/r B-ALL). However, the long-term outcome and the factors that influence the efficacy need further exploration. Here we report the outcome of 51 r/r B-ALL patients from a non-randomized, Phase II clinical trial (ClinicalTrials.gov number: NCT02735291). The primary outcome shows that the overall remission rate (complete remission with or without incomplete hematologic recovery) is 80.9%. The secondary outcome reveals that the overall survival (OS) and relapse-free survival (RFS) rates at 1 year are 53.0 and 45.0%, respectively. The incidence of grade 4 adverse reactions is 6.4%. The trial meets pre-specified endpoints. Further analysis shows that patients with extramedullary diseases (EMDs) other than central nervous system (CNS) involvement have the lowest remission rate (28.6%). The OS and RFS in patients with any subtype of EMDs, higher Tregs, or high-risk genetic factors are all significantly lower than that in their corresponding control cohorts. EMDs and higher Tregs are independent high-risk factors respectively for poor OS and RFS. Thus, these patient characteristics may hinder the efficacy of CAR T therapy.
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