| Literature DB >> 33620106 |
Rory McCulloch1, David Lewis1, Nicola Crosbie1, Toby A Eyre2, Simon Bolam3, Anita Arasaretnam4, Thomas Creasey5, Harshita Goradia6, Annabel McMillan7, Safia Dawi8, Samuel Harrison9, Oliver Miles10, Andrew Robinson11, David Dutton12, Matthew R Wilson13, Pam McKay13, George Follows11, Neil Phillips9, Russell Patmore8, Jonathan Lambert7, Mark Bishton6, Wendy Osborne5, Rosalynd Johnston4, Amy A Kirkwood14, Simon Rule15.
Abstract
Ibrutinib is an established treatment for relapsed/refractory (R/R) mantle cell lymphoma (MCL) and clinical trial data supports use at second line compared to later relapse. We aimed to investigate outcomes and tolerability for ibrutinib when given second line in a real-world setting. Our multicentre retrospective analysis included 211 R/R MCL patients, median age 73 years, receiving ibrutinib second-line within the United Kingdom's National Health Service. Overall response to ibrutinib was 69% (complete response 27%). The median progression-free survival (PFS) was 17·8 months (95% CI 13·1-22·2) and median overall survival (OS) 23·9 months (95% CI 15·0-32·8). Drug-related adverse event led to dose reduction in 10% of patients and discontinuation in 5%. In patients with progressive disease, accounting for 100 of 152 patients stopping ibrutinib, 43% received further systemic therapy. Post-ibrutinib rituximab, bendamustine and cytarabine (R-BAC) showed a trend toward improved survival compared to alternative systemic treatments (post-ibrutinib median OS 14·0 months, 95% CI 8·1-19·8, vs. 3·6 months, 95% CI 2·6-4·5, P = 0·06). Our study confirms the clinical benefit and good tolerability of ibrutinib at first relapse in a real-world population. Patients progressing on ibrutinib had limited survival but outcomes with R-BAC in select patients were promising.Entities:
Keywords: clinical aspects; ibrutinib; mantle cell lymphoma; post-ibrutinib outcomes
Year: 2021 PMID: 33620106 DOI: 10.1111/bjh.17363
Source DB: PubMed Journal: Br J Haematol ISSN: 0007-1048 Impact factor: 6.998