Challenges and optimal strategies of CAR T therapy for hematological malignancies.
10.1097/CM9.0000000000002476
- Author:
Yajing ZHANG
1
;
Yang XU
2
;
Xiuyong DANG
3
;
Zeyu ZHU
3
;
Wenbin QIAN
2
;
Aibin LIANG
3
;
Weidong HAN
1
Author Information
1. Department of Bio-Therapeutics, The First Medical Centre, The General Hospital of Chinese People's Liberation Army, Beijing 100853, China.
2. Department of Hematology, The Second Affiliated Hospital, College of Medicine, Zhejiang University, Hangzhou, Zhejiang 310009, China.
3. Department of Hematology, Tongji Hospital of Tongji University, Shanghai 200065, China.
- Publication Type:Journal Article
- MeSH:
Humans;
Receptors, Chimeric Antigen/therapeutic use*;
Immunotherapy, Adoptive;
Hematologic Neoplasms/therapy*;
Treatment Outcome
- From:
Chinese Medical Journal
2023;136(3):269-279
- CountryChina
- Language:English
-
Abstract:
Remarkable improvement relative to traditional approaches in the treatment of hematological malignancies by chimeric antigen receptor (CAR) T-cell therapy has promoted sequential approvals of eight commercial CAR T products within last 5 years. Although CAR T cells' productization is now rapidly boosting their extensive clinical application in real-world patients, the limitation of their clinical efficacy and related toxicities inspire further optimization of CAR structure and substantial development of innovative trials in various scenarios. Herein, we first summarized the current status and major progress in CAR T therapy for hematological malignancies, then described crucial factors which possibly compromise the clinical efficacies of CAR T cells, such as CAR T cell exhaustion and loss of antigen, and finally, we discussed the potential optimization strategies to tackle the challenges in the field of CAR T therapy.