Examines tumor control in hematologic malignancies, suggesting improved T cell persistence.
Adoptive T cell therapy (ACT) has transformed the treatment of several hematologic malignancies, yet patients may develop resistance and disease come back. Moreover, durable responses in solid tumors remain by far challenging. A central goal in the field has been to improve the engraftment, expansion, and persistence of the infused T cells. For this reason, non-myeloablative lymphodepleting chemotherapy is incorporated into most ACT protocols to create “space” and cytokine availability for transferred cells by removing competing immune cells.
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Figueroa et al. (2026) studied this question.
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