Abstract
Chimeric antigen receptor (CAR) T-cell therapy is a promising immunotherapy based on genetically engineered T cells derived from patients. The introduction of CAR T-cell therapy has changed the treatment paradigm of patients with B-cell lymphoid malignancies. However, challenging issues including managing life-threatening toxicities related to CAR T-cell infusion and resistance to CAR T-cell therapy, leading to progression or relapse, remain. This review summarizes the issues with currently approved CAR T-cell therapies for patients with relapsed or refractory B-cell lymphoid malignancies, including lymphoma and myeloma. We focus on unique toxicities after CAR T-cell therapy, such as cytokine-related events and hematological toxicities, and the mechanisms underlying post-CAR T-cell failure.
| Original language | English |
|---|---|
| Pages (from-to) | 210-221 |
| Number of pages | 12 |
| Journal | Annals of Laboratory Medicine |
| Volume | 44 |
| Issue number | 3 |
| DOIs | |
| State | Published - May 2024 |
Keywords
- Chimeric antigen receptor
- Cytokine toxicity
- Efficacy
- Lymphoma
- Multiple myeloma