TY - JOUR
T1 - Rituximab Maintenance Added to Ibrutinib-Containing Therapy in Younger, Untreated Patients With Mantle Cell Lymphoma
T2 - Results From the TRIANGLE Trial
AU - Ladetto, Marco
AU - Gutmair, Katja
AU - Tavarozzi, Rita
AU - Pawlikowski, Alexandra
AU - Schomaker, Michael
AU - Doorduijn, Jeanette
AU - Giné, Eva
AU - Jerkeman, Mats
AU - Walewski, Jan
AU - Hutchings, Martin
AU - Mey, Ulrich
AU - Riise, Jon
AU - Trneny, Marek
AU - Vergote, Vibeke K.J.
AU - Horowitz, Netanel A.
AU - Gomes da Silva, Maria
AU - Leppä, Sirpa
AU - Jiang, Linmiao
AU - Stilgenbauer, Stephan
AU - Kerkhoff, Andrea
AU - Jachimowicz, Ron D.
AU - Heß, Georg
AU - van Meerten, Tom
AU - Wirths, Stefan
AU - Herhaus, Peter
AU - Novak, Urban
AU - Dierlamm, Judith
AU - Hänel, Mathias
AU - Hanoun, Christine
AU - Sonnevi, Kristina
AU - Visco, Carlo
AU - Castellino, Claudia
AU - Lemoli, Roberto Massimo
AU - Zilioli, Vittorio Ruggero
AU - Boccomini, Carola
AU - Pott, Christiane
AU - Klapper, Wolfram
AU - Schmidt, Christian
AU - Dreyling, Martin
AU - Hoster, Eva
AU - on behalf of the European MCL Network
N1 - Fase1Rigshospitalet
Publisher Copyright:
© 2026 by American Society of Clinical Oncology
PY - 2026
Y1 - 2026
N2 - The TRIANGLE trial established an ibrutinib-containing therapy without autologous stem-cell transplantation (ASCT) as the new standard for younger, treatment-naïve patients with mantle cell lymphoma (MCL). However, the benefit of rituximab maintenance (RM) within this novel standard is unclear. We investigated whether RM improves progression-free survival (PFS) and overall survival (OS) with acceptable toxicity when added to the experimental arms of TRIANGLE. This secondary analysis of TRIANGLE included patients randomly assigned to ibrutinib-containing therapy without (I) or with (A + I) ASCT who responded to induction/ASCT. RM was given per national and center practice. PFS and OS of patients with and without RM were compared with inverse probability of treatment weighted Kaplan-Meier curves and log-rank tests. Among responders after induction/ASCT (I: 274; A + I: 237), RM was given to 61% (I) and 64% (A + I). RM prolonged PFS in ibrutinib-containing treatment arms (I: log-rank test: P = .003, 4-year PFS probability RM v no RM, 85% v 73%; A + I: P < .001, 90% v 75%). There were trends toward prolonged OS in RM groups. RM groups were at higher risk of grade 3 to 5 infectious toxicity (I: 34% v 11%; A + I: 41% v 18%). Our findings support adding RM to BTK inhibitor treatments in younger, untreated patients with MCL to achieve prolonged remission.
AB - The TRIANGLE trial established an ibrutinib-containing therapy without autologous stem-cell transplantation (ASCT) as the new standard for younger, treatment-naïve patients with mantle cell lymphoma (MCL). However, the benefit of rituximab maintenance (RM) within this novel standard is unclear. We investigated whether RM improves progression-free survival (PFS) and overall survival (OS) with acceptable toxicity when added to the experimental arms of TRIANGLE. This secondary analysis of TRIANGLE included patients randomly assigned to ibrutinib-containing therapy without (I) or with (A + I) ASCT who responded to induction/ASCT. RM was given per national and center practice. PFS and OS of patients with and without RM were compared with inverse probability of treatment weighted Kaplan-Meier curves and log-rank tests. Among responders after induction/ASCT (I: 274; A + I: 237), RM was given to 61% (I) and 64% (A + I). RM prolonged PFS in ibrutinib-containing treatment arms (I: log-rank test: P = .003, 4-year PFS probability RM v no RM, 85% v 73%; A + I: P < .001, 90% v 75%). There were trends toward prolonged OS in RM groups. RM groups were at higher risk of grade 3 to 5 infectious toxicity (I: 34% v 11%; A + I: 41% v 18%). Our findings support adding RM to BTK inhibitor treatments in younger, untreated patients with MCL to achieve prolonged remission.
UR - https://www.scopus.com/pages/publications/105046957344
U2 - 10.1200/JCO-26-00705
DO - 10.1200/JCO-26-00705
M3 - Journal article
C2 - 42447409
AN - SCOPUS:105046957344
SN - 0732-183X
JO - Journal of Clinical Oncology
JF - Journal of Clinical Oncology
M1 - JCO-26-00705
ER -