PAX5 alterations in an infant case of KMT2A-rearranged leukemia with lineage switch

Lineage switch is a rare event at leukemic relapse. While mostly known to occur in KMT2A-rearranged infant leukemia, the underlying mechanism is yet to be depicted. This case report describes a female infant who achieved remission of KMT2A-MLLT3-rearranged acute monocytic leukemia, but 6 months thereafter, relapsed as KMT2A-MLLT3-rearranged acute lymphocytic leukemia. Whole exome sequencing of the bone marrow obtained pre-post lineage switch revealed two somatic mutations of PAX5 in the relapse sample. These two PAX5 alterations were suggested to be loss of function, thus to have played the driver role in the lineage switch from acute monocytic leukemia to acute lymphocytic leukemia.

Automated summary

This case report presents a female infant who experienced a lineage switch from KMT2A-MLLT3-rearranged acute monocytic leukemia to KMT2A-MLLT3-rearranged acute lymphocytic leukemia. Whole exome sequencing revealed two somatic mutations of PAX5 in the relapse sample, which were suggested to be loss of function and potentially driving the lineage switch.