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McCulloch, Rory

0000-0003-0090-7174

Mayo Clinic

Department of Haematology, Gloucestershire Hospitals NHS Foundation Trust, Gloucester, United Kingdom.

Citations 1

Time to progression of disease and outcomes with second-line BTK inhibitors in relapsed/refractory mantle cell lymphoma
Villa, Diego , Visco, Carlo , Crosbie, Nicola, McCulloch, Rory , Buege, Michael J. , Kumar, Anita , Bond, David A. , Maurer, Matthew J. , Thanarajasingam, Gita , Lewis, Katharine L. , Cheah, Chan Y. , Bæch, Joachim , Kugathasan, Laveniya , Lewis, David , Visco, Carlo , McCulloch, Rory , Buege, Michael J , Kumar, Anita , Bond, David A , Paludo, Jonas , Maurer, Matthew , Lewis, Katharine L , Cheah, Chan Yoon , Baech, Joachim , El-Galaly, Tarec C , Scott, David W , Gerrie, Alina S , Jiang, Aixiang , Paludo, Jonas , El‐Galaly, Tarec Christoffer , Scott, David W. , Gerrie, Alina S.

Blood Advances | June 12, 2023 | Volume: 7 | Issue: 16 | Pages: 4576-4585

10.1182/bloodadvances.2023009804 Get It

Abstract Time to progression of disease (POD) after first-line (1L) therapy is prognostic in mantle cell lymphoma (MCL), although studies have included a broad range of 1L, second-line (2L), and subsequent lines of therapy. The purpose of this study was to evaluate the factors predicting outcomes in patients with relapsed/refractory (R/R) MCL exclusively initiating 2L Bruton’s tyrosine kinase inhibitors (BTKis) after 1L rituximab-containing therapy. Patients were accrued from 8 international centers (7 main, 1 validation cohort). Multivariable models evaluating the association between time to POD and clinical/pathologic factors were constructed and converted into nomograms and prognostic indexes predicting outcomes in this population. A total of 360 patients were included, including 160 in the main cohort and 200 in the validation cohort. Time to POD, Ki67 ≥ 30%, and MCL International Prognostic Index (MIPI) were associated with progression-free survival (PFS2) and overall survival (OS2) from the start of 2L BTKis. C-indexes were consistently ≥0.68 in both cohorts. Web/application-based calculators based on nomograms and prognostic indexes to estimate PFS2 and OS2 were constructed. The 2L BTKi MIPI identifies 3 groups with distinct 2-year PFS2, including high risk (14%), intermediate risk (50%), and low risk (64%). Time to POD, Ki67, and MIPI are associated with survival outcomes in patients with R/R MCL receiving 2L BTKis. Simple clinical models incorporating these variables may assist in planning for alternative therapies such as chimeric antigen receptor T-cell therapy, allogeneic stem cell transplantation, or novel agents with alternative mechanisms of action.