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ORIGINAL RESEARCH article

Front. Immunol.

Sec. Cancer Immunity and Immunotherapy

Volume 16 - 2025 | doi: 10.3389/fimmu.2025.1532460

This article is part of the Research Topic Mechanisms and Therapeutic Opportunities of T Cell Impairment in Cancer Immunity and Immunotherapy View all 9 articles

Combination autologous stem cell transplantation with chimeric antigen receptor T-cell therapy for refractory/relapsed B-cell lymphoma: A single-arm clinical study

Provisionally accepted
Danyang Li Danyang Li 1*Rui Liu Rui Liu 1*Zhonghua Fu Zhonghua Fu 1*Fan Yang Fan Yang 1*Lixia Ma Lixia Ma 1*Yuelu Guo Yuelu Guo 1*Miaomiao Cao Miaomiao Cao 1*Yang Lei Yang Lei 1*Yimeng Dou Yimeng Dou 1*Xuenan Zhang Xuenan Zhang 1*Yan Gao Yan Gao 1*Bian Wei Bian Wei 1*Biping Deng Biping Deng 1*Xiaoyan Ke Xiaoyan Ke 1,2*Kai Hu Kai Hu 1*
  • 1 Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
  • 2 Department of Hematology, Peking University Third Hospital, Beijing, China

The final, formatted version of the article will be published soon.

    Autologous stem cell transplantation (ASCT) and chimeric antigen receptor T-cells (CAR-T) have been used as consolidation therapies for patients with refractory/recurrent B cell non-Hodgkin's lymphoma (R/R B-NHL) in remission after second-line chemotherapy or salvage therapy. However, patients with different pathological subtypes and remission states may benefit differently from ASCT or CAR-T cell therapy. Furthermore, consolidation treatment involving ASCT or CAR-T cells still poses a significant risk of disease relapse. We conducted a retrospective, single-arm study of 47 patients with R/R B-NHL, and found that the combination of ASCT and CAR-T therapy improved the 3-year progression-free survival (PFS) and overall survival (OS) rates to 66.04% (95%CI: 48.311-78.928) and 72.442% (95%CI: 53.46-84.708) respectively. Furthermore, the combination therapy has no serious adverse events. Thus, ASCT combined with CAR-T cell therapy is effective against multiple subtypes of R/R B-NHL, and can effectively prolong the long-term survival of patients.

    Keywords: B-NHL, car-t, ASCT, combination therapy, refractory/relapsed B-cell lymphoma

    Received: 22 Nov 2024; Accepted: 10 Feb 2025.

    Copyright: © 2025 Li, Liu, Fu, Yang, Ma, Guo, Cao, Lei, Dou, Zhang, Gao, Wei, Deng, Ke and Hu. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence:
    Danyang Li, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Rui Liu, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Zhonghua Fu, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Fan Yang, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Lixia Ma, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Yuelu Guo, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Miaomiao Cao, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Yang Lei, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Yimeng Dou, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Xuenan Zhang, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Yan Gao, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Bian Wei, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Biping Deng, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Xiaoyan Ke, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China
    Kai Hu, Department of Lymphoma and Myeloma Research Center, Beijing GoBroad Hospital, Beijing, China

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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