TY - JOUR
T1 - Real-world experience among patients with relapsed/refractory mantle cell lymphoma after Bruton tyrosine kinase inhibitor failure in Europe
T2 - The SCHOLAR-2 retrospective chart review study
AU - Hess, Georg
AU - Dreyling, Martin
AU - Oberic, Lucie
AU - Gine, Eva
AU - Zinzani, Pier Luigi
AU - Linton, Kim
AU - Vilmar, Adam
AU - Jerkeman, Mats
AU - Chen, Jenny M.H.
AU - Ohler, Anke
AU - Stilgenbauer, Stephan
AU - Thieblemont, Catherine
AU - Lambert, Jonathan
AU - Zilioli, Vittorio Ruggero
AU - Sancho, Juan Manuel
AU - Jiménez-Ubieto, Ana
AU - Fischer, Luca
AU - Eyre, Toby A.
AU - Keeping, Sam
AU - Park, Julie E.
AU - Wu, James J.
AU - Siddiqi, Rubina
AU - Reitan, John
AU - Wade, Sally
AU - Salles, Gilles
N1 - Publisher Copyright:
© 2022 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.
PY - 2023/8/16
Y1 - 2023/8/16
N2 - Mantle cell lymphoma (MCL) after relapse is associated with poor prognosis. No standard of care exists and available evidence for treatments is limited, particularly in patients who fail Bruton tyrosine kinase inhibitor (BTKi) therapy. This multicentre retrospective chart review study, SCHOLAR-2, addresses this knowledge gap and reports on data collected from 240 patients with relapsed/refractory MCL in Europe who were treated with BTKi-based therapy between July 2012 and July 2018, and had experienced disease progression while on BTKi therapy or discontinued BTKi therapy due to intolerance. The median overall survival (OS) from initiation of first BTKi therapy was 14.6 months (95% confidence interval [CI] 11.6–20.0) in the overall cohort, 5.5 months (95% CI 3.9–8.2) in 91 patients without post-BTKi therapy, and 23.8 months (95% CI 18.9–30.1) in 149 patients who received post-BTKi therapy (excluding chimeric antigen receptor T-cell treatment). In the latter group, patients received a median of one (range, one to seven) line of post-BTKi therapy, with lenalidomide-containing regimens and bendamustine plus rituximab being the most frequently administered; the median OS from initiation of first post-BTKi therapy was 9.7 months (95% CI 6.3–12.7). These results provide a benchmark for survival in patients with R/R MCL receiving salvage therapy after BTKi failure.
AB - Mantle cell lymphoma (MCL) after relapse is associated with poor prognosis. No standard of care exists and available evidence for treatments is limited, particularly in patients who fail Bruton tyrosine kinase inhibitor (BTKi) therapy. This multicentre retrospective chart review study, SCHOLAR-2, addresses this knowledge gap and reports on data collected from 240 patients with relapsed/refractory MCL in Europe who were treated with BTKi-based therapy between July 2012 and July 2018, and had experienced disease progression while on BTKi therapy or discontinued BTKi therapy due to intolerance. The median overall survival (OS) from initiation of first BTKi therapy was 14.6 months (95% confidence interval [CI] 11.6–20.0) in the overall cohort, 5.5 months (95% CI 3.9–8.2) in 91 patients without post-BTKi therapy, and 23.8 months (95% CI 18.9–30.1) in 149 patients who received post-BTKi therapy (excluding chimeric antigen receptor T-cell treatment). In the latter group, patients received a median of one (range, one to seven) line of post-BTKi therapy, with lenalidomide-containing regimens and bendamustine plus rituximab being the most frequently administered; the median OS from initiation of first post-BTKi therapy was 9.7 months (95% CI 6.3–12.7). These results provide a benchmark for survival in patients with R/R MCL receiving salvage therapy after BTKi failure.
KW - Bruton tyrosine kinase inhibitor
KW - mantle cell lymphoma
KW - post-BTKi
KW - real-world evidence
KW - survival
UR - http://www.scopus.com/inward/record.url?scp=85140099104&partnerID=8YFLogxK
U2 - 10.1111/bjh.18519
DO - 10.1111/bjh.18519
M3 - Review article
C2 - 36257914
AN - SCOPUS:85140099104
SN - 0007-1048
VL - 202
SP - 749
EP - 759
JO - British Journal of Haematology
JF - British Journal of Haematology
IS - 4
ER -