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letter
. 2022 Oct 29;7(1):88–91. doi: 10.1182/bloodadvances.2022008634

Table 1.

First-line salvage therapy after ibrutinib progression/relapse

N = 25 (%) CR PR SD PD
BR and BO 6 (24) 4 0 0 2
R2 4 (16) 1 3 0 0
Phosphatidylinositol-3-kinase inhibitor 3 (12) 0 1 2 0
IR or IO 3 (12) 0 1 1 1
Others 9 (36) 1 2 4 2

BO, bendamustine and obinutuzumab; BR, bendamustine and rituximab; IO, ibrutinib and obinutuzumab; IR, ibrutinib and rituximab; R2, rituximab and lenalidomide (revlimid).

Among the 43 patients who progressed/relapsed after ibrutinib, only 25 received subsequent therapy.

Others: 5 included alkylator-based (nonbendamustine) therapies, 1 platinum-based, 2 anti-CD20 monoclonal antibodies, and 1 BCL-2 inhibitor.