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Advancing CAR T-Cell Therapy for Solid Tumors: Lessons Learned from Lymphoma Treatment
Chimeric antigen receptor (CAR) immunotherapy is one of the most promising modern approaches for the treatment of cancer. To date only two CAR T-cell products, Kymriah(®) and Yescarta(®), have been approved by the Food and Drug Administration (FDA) for the treatment of lymphoblastic leukemia and B-c...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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MDPI
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016531/ https://www.ncbi.nlm.nih.gov/pubmed/31947775 http://dx.doi.org/10.3390/cancers12010125 |
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author | Titov, Aleksei Valiullina, Aygul Zmievskaya, Ekaterina Zaikova, Ekaterina Petukhov, Alexey Miftakhova, Regina Bulatov, Emil Rizvanov, Albert |
author_facet | Titov, Aleksei Valiullina, Aygul Zmievskaya, Ekaterina Zaikova, Ekaterina Petukhov, Alexey Miftakhova, Regina Bulatov, Emil Rizvanov, Albert |
author_sort | Titov, Aleksei |
collection | PubMed |
description | Chimeric antigen receptor (CAR) immunotherapy is one of the most promising modern approaches for the treatment of cancer. To date only two CAR T-cell products, Kymriah(®) and Yescarta(®), have been approved by the Food and Drug Administration (FDA) for the treatment of lymphoblastic leukemia and B-cell lymphoma. Administration of CAR T-cells to control solid tumors has long been envisaged as one of the most difficult therapeutic tasks. The first two clinical trials conducted in sarcoma and neuroblastoma patients showed clinical benefits of CAR T-cells, yet multiple obstacles still hold us back from having accessible and efficient therapy. Why did such an effective treatment for relapsed and refractory hematological malignancies demonstrate only relatively modest efficiency in the context of solid tumors? Is it due to the lucky selection of the “magic” CD19 antigen, which might be one of a kind? Or do lymphomas lack the immunosuppressive features of solid tumors? Here we review the existing knowledge in the field of CAR T-cell therapy and address the heterogeneity of solid tumors and their diverse strategies of immunoevasion. We also provide an insight into prospective developments of CAR T-cell technologies against solid tumors. |
format | Online Article Text |
id | pubmed-7016531 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-70165312020-03-04 Advancing CAR T-Cell Therapy for Solid Tumors: Lessons Learned from Lymphoma Treatment Titov, Aleksei Valiullina, Aygul Zmievskaya, Ekaterina Zaikova, Ekaterina Petukhov, Alexey Miftakhova, Regina Bulatov, Emil Rizvanov, Albert Cancers (Basel) Review Chimeric antigen receptor (CAR) immunotherapy is one of the most promising modern approaches for the treatment of cancer. To date only two CAR T-cell products, Kymriah(®) and Yescarta(®), have been approved by the Food and Drug Administration (FDA) for the treatment of lymphoblastic leukemia and B-cell lymphoma. Administration of CAR T-cells to control solid tumors has long been envisaged as one of the most difficult therapeutic tasks. The first two clinical trials conducted in sarcoma and neuroblastoma patients showed clinical benefits of CAR T-cells, yet multiple obstacles still hold us back from having accessible and efficient therapy. Why did such an effective treatment for relapsed and refractory hematological malignancies demonstrate only relatively modest efficiency in the context of solid tumors? Is it due to the lucky selection of the “magic” CD19 antigen, which might be one of a kind? Or do lymphomas lack the immunosuppressive features of solid tumors? Here we review the existing knowledge in the field of CAR T-cell therapy and address the heterogeneity of solid tumors and their diverse strategies of immunoevasion. We also provide an insight into prospective developments of CAR T-cell technologies against solid tumors. MDPI 2020-01-03 /pmc/articles/PMC7016531/ /pubmed/31947775 http://dx.doi.org/10.3390/cancers12010125 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Titov, Aleksei Valiullina, Aygul Zmievskaya, Ekaterina Zaikova, Ekaterina Petukhov, Alexey Miftakhova, Regina Bulatov, Emil Rizvanov, Albert Advancing CAR T-Cell Therapy for Solid Tumors: Lessons Learned from Lymphoma Treatment |
title | Advancing CAR T-Cell Therapy for Solid Tumors: Lessons Learned from Lymphoma Treatment |
title_full | Advancing CAR T-Cell Therapy for Solid Tumors: Lessons Learned from Lymphoma Treatment |
title_fullStr | Advancing CAR T-Cell Therapy for Solid Tumors: Lessons Learned from Lymphoma Treatment |
title_full_unstemmed | Advancing CAR T-Cell Therapy for Solid Tumors: Lessons Learned from Lymphoma Treatment |
title_short | Advancing CAR T-Cell Therapy for Solid Tumors: Lessons Learned from Lymphoma Treatment |
title_sort | advancing car t-cell therapy for solid tumors: lessons learned from lymphoma treatment |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7016531/ https://www.ncbi.nlm.nih.gov/pubmed/31947775 http://dx.doi.org/10.3390/cancers12010125 |
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