Chimeric antigen receptor T cell therapies for multiple myeloma
Abstract Multiple myeloma (MM) is the second most common hematologic malignancy and remains incurable despite the advent of numerous new drugs such as proteasome inhibitors (PIs), immunomodulatory agents (IMiDs), and monoclonal antibodies. There is an unmet need to develop novel therapies for refrac...
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doaj-d5273e61a05c4f8899ce427199920b242020-11-25T04:02:51ZengBMCJournal of Hematology & Oncology1756-87222019-11-0112111210.1186/s13045-019-0823-5Chimeric antigen receptor T cell therapies for multiple myelomaChao Wu0Lina Zhang1Qierra R. Brockman2Fenghuang Zhan3Lijuan Chen4Department of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province HospitalDepartment of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province HospitalDepartment of Medicine, Division of Hematology, Oncology and Blood and Marrow Transplantation and Holden Comprehensive Cancer Center, University of IowaDepartment of Medicine, Division of Hematology, Oncology and Blood and Marrow Transplantation and Holden Comprehensive Cancer Center, University of IowaDepartment of Hematology, The First Affiliated Hospital of Nanjing Medical University, Jiangsu Province HospitalAbstract Multiple myeloma (MM) is the second most common hematologic malignancy and remains incurable despite the advent of numerous new drugs such as proteasome inhibitors (PIs), immunomodulatory agents (IMiDs), and monoclonal antibodies. There is an unmet need to develop novel therapies for refractory/relapsed MM. In the past few years, chimeric antigen receptor (CAR)-modified T cell therapy for MM has shown promising efficacy in preclinical and clinical studies. Furthermore, the toxicities of CAR-T cell therapy are manageable. This article summarizes recent developments of CAR-T therapy in MM, focusing on promising targets, new technologies, and new research areas. Additionally, a comprehensive overview of antigen selection is presented along with preliminary results and future directions of CAR-T therapy development.http://link.springer.com/article/10.1186/s13045-019-0823-5Chimeric antigen receptorsMultiple myelomaImmunotherapyTumor immunology |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Chao Wu Lina Zhang Qierra R. Brockman Fenghuang Zhan Lijuan Chen |
spellingShingle |
Chao Wu Lina Zhang Qierra R. Brockman Fenghuang Zhan Lijuan Chen Chimeric antigen receptor T cell therapies for multiple myeloma Journal of Hematology & Oncology Chimeric antigen receptors Multiple myeloma Immunotherapy Tumor immunology |
author_facet |
Chao Wu Lina Zhang Qierra R. Brockman Fenghuang Zhan Lijuan Chen |
author_sort |
Chao Wu |
title |
Chimeric antigen receptor T cell therapies for multiple myeloma |
title_short |
Chimeric antigen receptor T cell therapies for multiple myeloma |
title_full |
Chimeric antigen receptor T cell therapies for multiple myeloma |
title_fullStr |
Chimeric antigen receptor T cell therapies for multiple myeloma |
title_full_unstemmed |
Chimeric antigen receptor T cell therapies for multiple myeloma |
title_sort |
chimeric antigen receptor t cell therapies for multiple myeloma |
publisher |
BMC |
series |
Journal of Hematology & Oncology |
issn |
1756-8722 |
publishDate |
2019-11-01 |
description |
Abstract Multiple myeloma (MM) is the second most common hematologic malignancy and remains incurable despite the advent of numerous new drugs such as proteasome inhibitors (PIs), immunomodulatory agents (IMiDs), and monoclonal antibodies. There is an unmet need to develop novel therapies for refractory/relapsed MM. In the past few years, chimeric antigen receptor (CAR)-modified T cell therapy for MM has shown promising efficacy in preclinical and clinical studies. Furthermore, the toxicities of CAR-T cell therapy are manageable. This article summarizes recent developments of CAR-T therapy in MM, focusing on promising targets, new technologies, and new research areas. Additionally, a comprehensive overview of antigen selection is presented along with preliminary results and future directions of CAR-T therapy development. |
topic |
Chimeric antigen receptors Multiple myeloma Immunotherapy Tumor immunology |
url |
http://link.springer.com/article/10.1186/s13045-019-0823-5 |
work_keys_str_mv |
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