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Evidence-Based Supplement Research
Evidence-Based Supplement Research

Clinical outcomes and spatial transcriptomic profiles of CD19/20 CAR-T therapy in relapsed or refractory B-cell non-Hodgkin's lymphoma.

  • 2026-05
  • Journal for immunotherapy of cancer 14(5)
    • Lixin Wang
    • Chuling Fang
    • Yuanyuan Zheng
    • Yuanyuan Xu
    • Wenfa Huang
    • Weiqiang Zhao
    • Yiran Wang
    • Jianglong Xia
    • Kun Tan
    • Lei Wang
    • Huixin Peng
    • Xiao Guo
    • Shuhong Wang
    • Lijun Wang
    • Lian Liu
    • Jingqiao Qiao
    • Xiangyu Meng
    • Ziqian He
    • Zonghua Wen
    • Chuan Yu
    • Junhui Mei
    • Hongxin Wang
    • Yisheng Li
    • Li Yu

Study Design

Type
Clinical Trial
Sample size
n = 32
Population
32 patients with relapsed or refractory B-cell non-Hodgkin's lymphoma (including 24 with diffuse large B-cell lymphoma)
Methods
Phase I/II expanded study; patients received bispecific CD19/20 CAR-T cells after lymphodepletion; spatial single-cell transcriptomic profiling of pretreatment biopsies in a subset
Funding
Unclear

Background

Relapsed or refractory (R/R) B-cell non-Hodgkin's lymphoma (B-NHL) remains a major therapeutic challenge despite CD19-directed chimeric antigen receptor (CAR) T-cell therapies, with treatment failure often driven by antigen escape and limited CAR-T persistence. Dual targeting of CD19 and CD20 may mitigate antigen loss. We conducted an expanded phase I/II study of bispecific CD19/20 CAR-T cells and incorporated spatially resolved single-cell transcriptomics to evaluate tumor-intrinsic and microenvironmental factors of clinical response.

Methods

Patients with R/R B-NHL received CD19/20 CAR-T cells following lymphodepletion. Efficacy, safety, CAR-T expansion/persistence, and B-cell reconstitution were assessed. Pretreatment tumor biopsies from five patients with divergent outcomes underwent spatial single-cell transcriptomic profiling.

Results

32 patients were treated, including 24 with diffuse large B-cell lymphoma. Among 31 evaluable patients, the best overall response rate was 74%, including 58% achieving complete remission. Median progression-free and overall survival were 6.8 and 22.1 months, respectively. Response rates were higher in patients with normal lactate dehydrogenase. CAR-T expansion peaked on days 7-17, and persistence exceeded 500 days in long-term responders. Cytokine release syndrome occurred in 53% (12% grade ≥3) and immune effector cell-associated neurotoxicity syndrome in 9% (all grade 3), with no lasting deficits. Spatial profiling identified two dominant tumor architectures: (1) a B-cell-dominant phenotype, in which durable remission was associated with heightened apoptotic competence in malignant B cells, and (2) a fibroblast-enriched and monocyte/macrophage-enriched phenotype, in which response correlated with a chemokine-rich, T-cell-permissive microenvironment.

Conclusions

Bispecific CD19/20 CAR-T therapy produced durable clinical activity with manageable toxicity. Spatial single-cell analysis reveals distinct tumor-intrinsic and microenvironmental features associated with CAR-T responsiveness, providing a spatially informed framework for understanding heterogeneous therapeutic outcomes.

Trial registration number

NCT04723914.

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