CAR T–associated toxicities
Acute phase (D0-30) . | Late phase (D30+) . |
---|---|
• CRS | • Persistent cytopenias |
• Immune effector cell–associated neurotoxicity syndrome | • B-cell aplasia and hypogammaglobulinemia |
• Cytopenias | • ?IVIG replacement |
• Macrophage activation syndrome or hemophagocytic lymphohistiocytosis, is a very rare and severe form | • T-cell deficiency |
• Disseminated intravascular coagulopathy | • Pneumocystis jirovecii pneumonia and varicella-zoster virus prophylaxis, other? |
• Infection prophylaxis | |
• B-cell aplasia and hypogammaglobulinemia | • Residual effects of acute toxicity |
• Life threatening if not managed by expert multidisciplinary team | • Delayed CRS and neurotoxicity is rare but can occur. |
• Tumor lysis is rare and probably varies by disease and disease burden. | • Impaired quality of life: fatigue, memory issues, not yet well described |
Acute phase (D0-30) . | Late phase (D30+) . |
---|---|
• CRS | • Persistent cytopenias |
• Immune effector cell–associated neurotoxicity syndrome | • B-cell aplasia and hypogammaglobulinemia |
• Cytopenias | • ?IVIG replacement |
• Macrophage activation syndrome or hemophagocytic lymphohistiocytosis, is a very rare and severe form | • T-cell deficiency |
• Disseminated intravascular coagulopathy | • Pneumocystis jirovecii pneumonia and varicella-zoster virus prophylaxis, other? |
• Infection prophylaxis | |
• B-cell aplasia and hypogammaglobulinemia | • Residual effects of acute toxicity |
• Life threatening if not managed by expert multidisciplinary team | • Delayed CRS and neurotoxicity is rare but can occur. |
• Tumor lysis is rare and probably varies by disease and disease burden. | • Impaired quality of life: fatigue, memory issues, not yet well described |