Phase 3 SELENE study: ibrutinib plus BR/R-CHOP in previously treated patients with follicular or marginal zone lymphoma

Blood Adv. 2023 Nov 28;7(22):7141-7150. doi: 10.1182/bloodadvances.2023010298.

Abstract

The phase 3 SELENE study evaluated ibrutinib + chemoimmunotherapy (CIT; bendamustine and rituximab [BR]; or rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisone [R-CHOP]) for patients with relapsed/refractory (R/R) follicular lymphoma (FL) or marginal zone lymphoma (MZL). Adult patients who had received ≥1 prior line of CIT were randomized 1:1 to oral ibrutinib (560 mg) or placebo daily, plus 6 cycles of BR/R-CHOP. The primary end point was investigator-assessed progression-free survival (PFS). Overall, 403 patients were randomized to ibrutinib + CIT (n = 202) or placebo + CIT (n = 201). Most patients received BR (90.3%) and had FL (86.1%). With a median follow-up of 84 months, median PFS was 40.5 months in the ibrutinib + CIT arm and 23.8 months in the placebo + CIT arm (hazard ratio [HR], 0.806; 95% confidence interval [CI], 0.626-1.037; P = .0922). Median overall survival was not reached in either arm (HR, 0.980; 95% CI, 0.686-1.400). Grade ≥3 treatment-emergent adverse events (TEAEs) were reported in 85.6% and 75.4% of patients in the ibrutinib + CIT and placebo + CIT arms, respectively. In each arm, 13 patients had TEAEs leading to death. The addition of ibrutinib to CIT did not significantly improve PFS compared with placebo + CIT. The safety profile was consistent with known profiles of ibrutinib and CIT. This trial was registered at www.clinicaltrials.gov as #NCT01974440.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Adult
  • Bendamustine Hydrochloride / therapeutic use
  • Cyclophosphamide / adverse effects
  • Doxorubicin / adverse effects
  • Humans
  • Lymphoma, B-Cell, Marginal Zone* / drug therapy
  • Lymphoma, Follicular* / drug therapy
  • Piperidines / therapeutic use
  • Prednisone / adverse effects
  • Rituximab / adverse effects
  • Vincristine / adverse effects

Substances

  • Rituximab
  • Bendamustine Hydrochloride
  • ibrutinib
  • Piperidines
  • Vincristine
  • Cyclophosphamide
  • Prednisone
  • Doxorubicin

Associated data

  • ClinicalTrials.gov/NCT01974440