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CAR T-Cell Therapy in Children with Solid Tumors

期刊

JOURNAL OF CLINICAL MEDICINE
卷 12, 期 6, 页码 -

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MDPI
DOI: 10.3390/jcm12062326

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adoptive cell therapy; CAR T-cells; solid tumors

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Traditional cancer treatments have limited efficacy, highlighting the importance of innovative methods like CAR T-cell therapy, which has shown remarkable success in treating pediatric hematological malignancies. By modifying the patient's own lymphocytes to recognize and destroy specific tumor cells, CAR-T is a personalized and promising therapy. While its effectiveness in treating solid tumors is still being researched, CAR-T has the potential to significantly improve outcomes for children with limited treatment options.
The limited efficacy of traditional cancer treatments, including chemotherapy, radiotherapy, and surgery, emphasize the significance of employing innovative methods. CAR (Chimeric Antigen Receptor) T-cell therapy remains the most revolutionizing treatment of pediatric hematological malignancies and solid tumors. Patient's own lymphocytes are modified ex-vivo using gene transfer techniques and programmed to recognize and destroy specific tumor cells regardless of MHC receptor, which probably makes CAR-T the most personalized therapy for the patient. With continued refinement and optimization, CAR-T cell therapy has the potential to significantly improve outcomes and quality of life for children with limited treatment options. It has shown remarkable success in treating hematological malignancies, such as acute lymphoblastic leukemia (ALL) and non-Hodgkin lymphoma (NHL). However, its effectiveness in treating solid tumors is still being investigated and remains an area of active research. In this review we focus on solid tumors and explain the concept of CAR modified T cells, and discuss some novel CAR designs that are being considered to enhance the safety of CAR T-cell therapy in under-mentioned cancers. Furthermore, we summarize the most crucial recent reports concerning the solid tumors treatment in children. In the end we provide a short summary of many challenges that limit the therapeutic efficacy of CAR-T in solid tumors, such as antigen escape, immunosuppressive microenvironment, poor trafficking, and tumor infiltration, on-target off-tumor effects and general toxicity.

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