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Association details:
Evidence:
Evidence Level:
Sensitive: C3 – Early Trials
New
Source:
Title:

Brigatinib in patients with ALK-positive anaplastic large cell lymphoma who have failed brentuximab vedotin

Published date:
06/09/2023
Excerpt:
ALCL was refractory to the last treatment in 10/15 pts. 10/11 pts had detectable ALK transcript in blood by RT-PCR...After a median follow-up of 1.3 years, 1-year PFS and OS were 72% and 85%, respectively...Brigatinib showed high efficacy, including in pts who have failed crizotinib, and was well tolerated.
DOI:
10.1002/hon.3164_373
Evidence Level:
Sensitive: C3 – Early Trials
Source:
Title:

RIGATINIB IN PATIENTS WITH ALK-POSITIVE ANAPLASTIC LARGE CELLLYMPHOMA WHO HAVE FAILED BRENTUXIMAB VEDOTIN

Published date:
05/11/2023
Excerpt:
ALCL was refractory to the last treatment in 10/15 pts. 10/11 pts had detectable ALK transcript in blood by RT-PCR. Pts received brigatinib at a dose of 180 mg once daily….Brigatinib showed high efficacy, including in pts who have failed crizotinib, and was well tolerated.
Evidence Level:
Sensitive: D – Preclinical
Title:

Patient-derived xenograft models of ALK+ ALCL reveal preclinical promise for therapy with brigatinib

Published date:
06/25/2023
Excerpt:
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.
DOI:
10.1111/bjh.18953