Real-World Treatment Outcomes Among Relapsed/Refractory Patients with Mantle Cell Lymphoma Treated with Ibrutinib or Acalabrutinib
Author(s)
Crawford S1, Lafeuille MH2, Emond B2, Harb D1, Voladarsky R1, Chen N1, Karve S1
1Pharmacyclics LLC, an AbbVie Company, South San Francisco, CA, USA, 2Analysis Group, Inc., Montreal, QC, Canada
Presentation Documents
OBJECTIVES: Evaluate treatment outcomes among patients with mantle cell lymphoma (MCL) treated with the Bruton’s tyrosine kinase inhibitors (BTKis) ibrutinib or acalabrutinib in second- or later-line therapy (2L+).
METHODS: Adults with MCL who initiated single-agent ibrutinib or acalabrutinib in 2L+ (index date) on or after 10/31/2017 (date of acalabrutinib approval for MCL) were analyzed using insurance claims from Optum’s de-identified Clinformatics® Data Mart Database (04/30/2017-12/31/2021). Treatment persistence (defined as not having a gap for >90 days in treatment) was evaluated among patients with sufficient potential follow-up (index date at least 15 months before end of data, with at least 60 days continuous enrollment post-index) to observe discontinuation; comparisons between cohorts were conducted using a multivariate Cox proportional hazards model. All models were adjusted for baseline characteristics observed during the 6-month period pre-index.
RESULTS: A total of 50 patients treated with ibrutinib (mean age: 76.3 years; 58.0% male) and 48 patients treated with acalabrutinib (mean age: 76.4 years; 64.6% male) were included. Among patients with sufficient potential follow-up post-index, 62.8% and 75.0% of patients discontinued ibrutinib and acalabrutinib, respectively, with a median time to discontinuation of 8.9 and 5.7 months, respectively (adjusted hazard ratio=0.79; P=0.496). Among patients without use of a BTKi in a preceding line of therapy with sufficient potential follow-up, median time to discontinuation was 8.9 and 6.9 months for ibrutinib and acalabrutinib cohorts, respectively (adjusted hazard ratio=0.81; P=0.610). Among patients receiving chemoimmunotherapy in first-line (1L) and with sufficient potential follow-up, median time to discontinuation was 9.3 and 4.4 months for ibrutinib and acalabrutinib, respectively (adjusted hazard ratio=0.47; P=0.085).
CONCLUSIONS: Treatment persistence was similar in patients with MCL treated with ibrutinib or acalabrutinib in 2L+, with slightly longer median time to discontinuation observed among patients treated with ibrutinib.
Conference/Value in Health Info
Value in Health, Volume 26, Issue 6, S2 (June 2023)
Code
SA34
Topic
Study Approaches
Disease
Drugs