Table 1.

Comparison of considerations for intensification strategies for relapsed follicular lymphoma—CAR-T vs autologous transplant

Autologous transplantCAR-T
Requires chemosensitive disease Yes No 
Potential benefit limited to early in relapsed course Yes No 
Short-term toxicities Mucositis, infection, sepsis, pneumonitis, poor engraftment CRS, ICANS, cytopenia, infection 
Long-term toxicities Therapy-related myeloid malignancies B-cell aplasia, hypogammaglobulinemia, cytopenia 
Other considerations Need for adequate marrow reserve for stem cell collection, eligibility limited to fit patients Need for adequate lymphocyte count, wait time for and requirement of successful T-cell manufacturing, likely lower fitness requirement than autologous transplant 
Autologous transplantCAR-T
Requires chemosensitive disease Yes No 
Potential benefit limited to early in relapsed course Yes No 
Short-term toxicities Mucositis, infection, sepsis, pneumonitis, poor engraftment CRS, ICANS, cytopenia, infection 
Long-term toxicities Therapy-related myeloid malignancies B-cell aplasia, hypogammaglobulinemia, cytopenia 
Other considerations Need for adequate marrow reserve for stem cell collection, eligibility limited to fit patients Need for adequate lymphocyte count, wait time for and requirement of successful T-cell manufacturing, likely lower fitness requirement than autologous transplant 
*

Long-term follow-up evaluating both risk and benefit in large cohorts of patients with FL receiving CAR-T is limited.

ICANS, immune effector cell-associated neurotoxicity syndrome.

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