In this issue of Blood, Nagel et al provide evidence supporting the presence of premalignant leukemic clones in nonlymphoid compartments of patients with BCR-ABL1–positive B-cell precursor acute lymphoblastic leukemia (ALL) as a cause of lineage switch after CD19 immunotherapy, extending the lineage switch mechanism beyond mixed-lineage leukemia (MLL)-rearranged ALL.(1) This observation suggests that CD19-targeted therapies alone may not suffice in the eradication of underlying disease in BCR-ABL1 p210- and p190-positive patients, and that strategies to target the stem cell compartment may be needed for durable remissions in this high-risk population.
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Shah et al. (2017) studied this question.
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