For all three PDXs, significant increases in EFS were seen for tumour-bearing animals treated with brigatinib relative to vehicle (MGS-A-x: p = 0.02494, MTK-A-x: p = 0.048, GR-ALCL-1: p = 0.01299; Figure 3G–I), with 3/8, 5/8 and 5/8 mice, respectively, showing a reduction in tumour volume (Figure 3D–F). Brigatinib treatment also led to a significant increase in EFS relative to crizotinib-treated mice...these data suggest that brigatinib administration is a well-tolerated approach for the treatment of PDX derived from ALK-positive ALCL involving the CNS that is either sensitive or r/r to crizotinib.