Background
Ibrutinib, a Bruton tyrosine kinase inhibitor, prolongs progression-free survival when added to immunochemotherapy as first line treatment. The ENRICH trial compared the chemotherapy-free combination of ibrutinib and the anti-CD20 antibody rituximab (ibrutinib–rituximab) with standard immunochemotherapy (R-CHOP [rituximab–cyclophosphamide, doxorubicin, vincristine, and prednisolone] or bendamustine–rituximab) in patients 60 years and older with untreated mantle-cell lymphoma.
Methods
This randomised, open-label, phase 2/3 superiority trial was performed at 66 sites in the UK, Sweden, Norway, Finland, and Denmark. Patients 60 years and older with untreated mantle-cell lymphoma (Ann–Arbor stage II–IV disease, an Eastern Cooperative Oncology Group performance-status score of 0–2) were randomly assigned to receive either rituximab plus immunochemotherapy or ibrutinib–rituximab in a 1:1 ratio, stratified by investigator choice of immunochemotherapy. Patients randomly allocated to the ibrutinib–rituximab (intervention) group received 560 mg oral ibrutinib daily in combination with six to eight cycles of 375 mg/m2 intravenous rituximab on day 1 of each cycle in the matched schedule of the pre-randomisation choice of immunochemotherapy (every 21 days for R-CHOP or every 28 days for rituximab–bendamustine). R-CHOP comprised 750 mg/m2 of cyclophosphamide, 50 mg/m2 of doxorubicin, and 1·4 mg/m2 vincristine on day 1 of each 21-day cycle, with 100 mg prednisolone on days 1–5 of each cycle. Rituximab–bendamustine comprised 90 mg/m2 of bendamustine on days 1 and 2 of each cycle, in combination with 375 mg/m2 rituximab on day 1 of each cycle. All responding patients in both groups at the end of induction received maintenance rituximab administered every 8 weeks for 2 years, and patients allocated to the intervention group continued ibrutinib until disease progression or unacceptable toxicity. The primary outcome was investigator-assessed progression-free survival, stratified by immunochemotherapy choice and analysed in the intention-to-treat population. The trial was registered with EudraCT (2015–000832–13) and is closed for recruitment.
Findings
Between Feb 15, 2016, and June 30, 2021, 397 patients were randomly allocated to immunochemotherapy (control) or ibrutinib–rituximab (intervention). Of the 397, 107 (27%) were pre-allocated to the immunochemotherapy choice of R-CHOP and 290 (73%) were pre-allocated to rituximab–bendamustine. In total, 198 were allocated to the control group (53 to R-CHOP and 145 to bendamustine–rituximab) and 199 were allocated to intervention. The median age was 74 years (IQR 70–77) for the intervention group and 74 years (70–78) in the control group. 296 patients (75%) were male and 101 patients (25%) were female; ethnicity data were not collected. At a median follow-up of 47·9 months, the median progression-free survival of ibrutinib–rituximab was superior to immunochemotherapy, with an adjusted hazard ratio (HR) of 0·69 (95% CI 0·52–0·90); p=0·0034. For those with pre-randomisation choice R-CHOP, the HR was 0·37 (0·22–0·62), and with bendamustine–rituximab, the HR was 0·91 (0·66–1·25). Across induction and maintenance, 67% of patients assigned to ibrutinib–rituximab and 70% of patients receiving immunotherapy reported grade 3 or above adverse events.
Interpretation
To our knowledge, this is the first randomised trial in untreated mantle-cell lymphoma to demonstrate significant improvement in progression-free survival for ibrutinib–rituximab compared to immunochemotherapy. This study suggests that ibrutinib–rituximab should be considered a new standard of care option for first-line treatment of older patients with mantle-cell lymphoma.
Funding
Cancer Research UK (C7627/A17938) and Johnson and Johnson Pharmaceuticals.
Author Affiliations
1 Department of Haematology, University Hospitals Plymouth NHS Trust, Plymouth, UK; 2 Department of Oncology, Skane University Hospital, Lund, Sweden; 3 Peninsula Medical School, University of Plymouth, Plymouth, UK; 4 Department of Clinical and Biomedical Sciences, University of Exeter, Exeter, Devon, UK; 5 Department of Immunology, Genetics and Pathology, Uppsala University, Uppsala, Sweden; 6 Zealand University Hospital Roskilde, Roskilde, Denmark; 7 Department of Oncology, Helsinki University Hospital Comprehensive Cancer Center, Helsinki, Finland; 8 Haematological Malignancy Diagnostic Service, Leeds Cancer Centre, Leeds Teaching Hospitals NHS Trust, Leeds, UK; 9 St Olav’s Hospital HF, Trondheim, Norway; 10 Department of Haematology, Sheffield Teaching Hospitals NHS Foundation Trust, Sheffield, UK; 11 Cancer Sciences Division, University of Southampton, Southampton, UK; 12 Linköping University Hospital, Linköping, Sweden; 13 Department of Haematology, University College London, London, UK; 14 Aarhus University Hospital, Aarhus, Denmark; 15 Odense University Hospital, Odense, Denmark; 16 Oslo University Hospital, Oslo, Norway; 17 Department of Haematology, Karolinska University Hospital, Stockholm; 18 Academic Unit of Translational Medical Sciences, University of Nottingham, Nottingham, UK; 19 Haematology and Cancer Centre, Churchill Hospital, Oxford University Hospitals NHS Trust, Oxford, UK; 20 AstraZeneca, Cambridge, UK
