Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2025 Jun 23.
doi: 10.1007/s11010-025-05329-5. Online ahead of print.

The challenges and progress of CAR-T cell therapy in the treatment of solid tumors

Affiliations
Review

The challenges and progress of CAR-T cell therapy in the treatment of solid tumors

Kai Cui et al. Mol Cell Biochem. .

Abstract

Current traditional cancer treatment methods include surgery, chemotherapy, radiotherapy, etc., which lack targeted killing functions and may damage normal tissues. Immunotherapy, targeted therapy, and personalized medicine have become promising methods for cancer treatment, providing more precise and effective treatment for patients. Among them, chimeric antigen receptor (CAR)-T cell therapy utilizes the immune system's T cells to recognize and attack tumor cells, showing promising therapeutic prospects. The FDA has approved CAR-T therapy for treating B-cell acute lymphoblastic leukemia, large B-cell lymphoma, and multiple myeloma, targeting CD-19 and B-cell maturation antigens. Despite success in hematologic cancers, CAR-T technology faces challenges in solid tumors, including a lack of reliable tumor-associated antigens, hypoxic cores, immunosuppressive tumor environments, enhanced reactive oxygen species, and decreased T cell infiltration. This review covers the advantages and disadvantages of various immunotherapy methods, highlights CAR-T therapy's evolution, summarizes CAR-T therapy's current status, lists promising therapeutic targets, and emphasizes the challenges CAR-T cell therapy faces.

Keywords: CAR-T cell therapy; Immunotherapy; Limitation; Solid tumor; Tumor-associated antigens.

PubMed Disclaimer

Conflict of interest statement

Declarations. Competing interest: The authors declare no competing interests.

Similar articles

References

    1. Martin-Liberal J, Ochoa de Olza M, Hierro C, Gros A, Rodon J, Tabernero J (2017) The expanding role of immunotherapy. Cancer Treat Rev 54:74–86. https://doi.org/10.1016/j.ctrv.2017.01.008 - DOI - PubMed
    1. Faramand RG, Locke FL (2025) Intermediate-affinity CD19-directed CAR T cell product obecabtagene autoleucel demonstrates favourable safety and efficacy in R/R B-ALL. Nat Rev Clin Oncol 22:161–162. https://doi.org/10.1038/s41571-025-00993-4 - DOI - PubMed
    1. Hadiloo K, Taremi S, Safa SH, Amidifar S, Esmaeilzadeh A (2024) The new era of immunological treatment, last updated and future consideration of CAR T cell-based drugs. Pharmacol Res 203:107158. https://doi.org/10.1016/j.phrs.2024.107158 - DOI - PubMed
    1. Borghaei H, Smith MR, Campbell KS (2009) Immunotherapy of cancer. Eur J Pharmacol 625:41–54. https://doi.org/10.1016/j.ejphar.2009.09.067 - DOI - PubMed - PMC
    1. Mellman I, Coukos G, Dranoff G (2011) Cancer immunotherapy comes of age. Nature 480:480–489. https://doi.org/10.1038/nature10673 - DOI - PubMed - PMC

LinkOut - more resources