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Rituximab Maintenance Added to Ibrutinib-Containing Therapy in Younger, Untreated Patients With Mantle Cell Lymphoma: Results From the TRIANGLE Trial

  • Marco Ladetto*
  • , Katja Gutmair
  • , Rita Tavarozzi
  • , Alexandra Pawlikowski
  • , Michael Schomaker
  • , Jeanette Doorduijn
  • , Eva Giné
  • , Mats Jerkeman
  • , Jan Walewski
  • , Martin Hutchings
  • , Ulrich Mey
  • , Jon Riise
  • , Marek Trneny
  • , Vibeke K.J. Vergote
  • , Netanel A. Horowitz
  • , Maria Gomes da Silva
  • , Sirpa Leppä
  • , Linmiao Jiang
  • , Stephan Stilgenbauer
  • , Andrea Kerkhoff
  • Ron D. Jachimowicz, Georg Heß, Tom van Meerten, Stefan Wirths, Peter Herhaus, Urban Novak, Judith Dierlamm, Mathias Hänel, Christine Hanoun, Kristina Sonnevi, Carlo Visco, Claudia Castellino, Roberto Massimo Lemoli, Vittorio Ruggero Zilioli, Carola Boccomini, Christiane Pott, Wolfram Klapper, Christian Schmidt, Martin Dreyling, Eva Hoster, on behalf of the European MCL Network
*Corresponding author for this work

Abstract

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.

Original languageEnglish
Article numberJCO-26-00705
JournalJournal of Clinical Oncology
ISSN0732-183X
DOIs
Publication statusE-pub ahead of print - 2026

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