The treatment landscape for acute lymphoblastic leukemia (ALL) has undergone significant transformation, particularly with the integration of immunotherapy into frontline regimens, according to Wendy Stock, MD, Anjuli Seth Nayak Professor of Medicine, UChicago Medicine. In this video, Stock says the focus is on the adolescent and young adult (AYA) population, a group for whom data on novel antibody use, such as blinatumomab, remains limited. While studies like E1910 and recent pediatric trials have demonstrated improved survival outcomes with blinatumomab, these findings are largely from older or high-risk populations. The challenge remains to define the best timing and dosage strategies for integrating immunotherapy into regimens for younger patients.
Importantly, the data show that even short courses of blinatumomab can significantly impact outcomes when added to standard therapy. However, chemotherapy remains essential, and the path forward lies in optimizing how immunotherapy is layered in to potentially reduce chemotherapy intensity and long-term toxicity.
Additional investigational therapies, such as CD22 antibody-drug conjugates and BH3 mimetics targeting BCL-2 family proteins, are on the horizon, alongside the evolving role of CAR T-cell therapies for both B- and T-cell ALL. The presentation also emphasizes the enduring importance of treatment adherence, particularly maintenance therapy, which continues to be a critical factor in long-term outcomes, especially in the pre-antibody treatment era.