Patients without del (17) (p13·1) zanubrutinib (group A; n=241) or bendamustine–rituximab (group B; n=238) and patients with del(17) (p13·1) zanubrutinib
Efficacy
mPFS was significantly improved in group A versus group B (HR 0·42 [95% CI 0·28 – 0·63]; p<0·0001)
24 months PFS: 85·5% in group A and 69·5% in group B
ORR: 94·6% in group A and 85·3% in group B
CR rate: 7% in group A and 15% in group B
Safety
Grade 1-2 any AEs: 41% vs 16% (group A vs group B)
Grade ≥3 AEs neutropenia 11% vs 51%, infections 16% vs 19%