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Review
. 2025 Jul;22(7):463-480.
doi: 10.1038/s41575-025-01062-y. Epub 2025 Apr 14.

CAR T cell therapies in gastrointestinal cancers: current clinical trials and strategies to overcome challenges

Affiliations
Review

CAR T cell therapies in gastrointestinal cancers: current clinical trials and strategies to overcome challenges

Hinrich Abken. Nat Rev Gastroenterol Hepatol. 2025 Jul.

Abstract

Despite multimodal treatment options, most gastrointestinal cancers are still associated with high mortality rates and poor responsiveness to immunotherapy. The unprecedented efficacy of chimeric antigen receptor (CAR)-engineered T cells in the treatment of haematological malignancies raised interest in translating CAR T cell therapies to the treatment of gastrointestinal cancers. Treatment of solid cancers with canonical CAR T cells faces substantial challenges, including the dense architecture of the tumour tissue, the tolerogenic environment with low tumour-intrinsic immunogenicity, the rareness of targetable tumour-selective antigens, the antigenic heterogeneity of cancer cells, and the profound metabolic and immune cell disbalances. This Review provides an overview of CAR T cell trials in the treatment of gastrointestinal cancers, discussing considerations relating to safety, efficacy, potential reasons for failure and options for improving CAR T cells for the future. In addition, lessons regarding how to improve efficacy are drawn from CAR T cells armed with adjuvants that sustain their activation within the hostile environment and activate resident immune cells. As the field is rapidly evolving, current treatment modalities and editing CAR T cell functionalities are being refined towards a potentially more successful CAR T cell therapy for gastrointestinal cancers.

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Conflict of interest statement

Competing interests: The author is co-inventor in patents and patent applications in the field of CAR T cells.

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References

    1. Posey, A. D., Young, R. M. & June, C. H. Future perspectives on engineered T cells for cancer. Trends Cancer 10, 687–695 (2024). - PubMed - DOI
    1. Abken, H. Building on synthetic immunology and T cell engineering: a brief journey through the history of chimeric antigen receptors. Hum. Gene Ther. 32, 1011–1028 (2021). - PubMed - PMC - DOI
    1. Pegram, H. J., Park, J. H. & Brentjens, R. J. CD28z CARs and armored CARs. Cancer J. 20, 127–133 (2014). - PubMed - PMC - DOI
    1. Chmielewski, M., Hombach, A. A. & Abken, H. Of CARs and TRUCKs: chimeric antigen receptor (CAR) T cells engineered with an inducible cytokine to modulate the tumor stroma. Immunol. Rev. 257, 83–90 (2014). - PubMed - DOI
    1. Tang, L., Pan, S., Wei, X., Xu, X. & Wei, Q. Arming CAR-T cells with cytokines and more: innovations in the fourth-generation CAR-T development. Mol. Ther. 31, 3146–3162 (2023). - PubMed - PMC - DOI

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