Predictive value of minimal residual disease for efficacy of rituximab maintenance in mantle cell lymphoma: Results from the European Mantle Cell Lymphoma Elderly trial Journal Article


Authors: Hoster, E.; Delfau-Larue, M. H.; MacIntyre, E.; Jiang, L.; Stilgenbauer, S.; Vehling-Kaiser, U.; Salles, G.; Thieblemont, C.; Tilly, H.; Wirths, S.; Feugier, P.; Hübel, K.; Schmidt, C.; Ribrag, V.; Kluin-Nelemans, J. C.; Dreyling, M.; Pott, C.; on behalf of the European MCL MRD Working Group and the European MCL Network
Article Title: Predictive value of minimal residual disease for efficacy of rituximab maintenance in mantle cell lymphoma: Results from the European Mantle Cell Lymphoma Elderly trial
Title Series: Journal of Clinical Oncology
Abstract: PURPOSEThe outcome of older patients with mantle cell lymphoma (MCL) has improved by the introduction of immunochemotherapy, followed by rituximab (R)-maintenance. Assessment of minimal residual disease (MRD) represents a promising tool for individualized treatment decisions and was a prospectively planned part of the European MCL Elderly trial. We investigated how MRD status influenced the efficacy of R-maintenance and how MRD can enable tailored consolidation strategies.PATIENTS AND METHODSPreviously untreated patients with MCL age 60 years or older have been randomly assigned to R versus interferon-alpha maintenance after response to rituximab, fludarabine, cyclophosphamide (R-FC) versus rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone (R-CHOP). MRD monitoring was performed by real-time quantitative polymerase chain reaction (qPCR) following EuroMRD guidelines.RESULTSA qPCR assay with a median sensitivity of 1 × 10-5 could be generated in 80% of 288 patients in an international, multicenter, multilaboratory setting. More extensive tumor dissemination facilitated the identification of a molecular marker. The efficacy of R-maintenance in clinical remission was confirmed for MRD-negative patients at the end of induction in terms of progression-free survival (PFS; hazard ratio [HR], 0.38 [95% CI, 0.21 to 0.63]) and overall survival (OS; HR, 0.37 [95% CI, 0.20 to 0.68]), particularly in R-CHOP-treated patients (PFS-HR, 0.23 [95% CI, 0.10 to 0.52]; OS-HR, 0.19 [95% CI, 0.07 to 0.52]). R-maintenance appeared less effective in MRD-positive patients (PFS-HR, 0.51 [95% CI, 0.26 to 1.02]) overall and after R-CHOP induction (PFS-HR, 0.59 [95% CI, 0.28 to 1.26]). R-FC achieved more frequent and faster MRD clearance compared with R-CHOP. MRD positivity in clinical remission after induction was associated with a short median time to clinical progression of approximately 1-1.7 years.CONCLUSIONThe results confirm the strong efficacy of R-maintenance in patients who are MRD-negative after induction. Treatment de-escalation for MRD-negative patients is discouraged by our results. More effective consolidation strategies should be explored in MRD-positive patients to improve their long-term prognosis. © 2024 American Society of Clinical Oncology.
Keywords: adult; controlled study; treatment response; aged; major clinical study; overall survival; fludarabine; drug efficacy; conference paper; alpha interferon; cancer patient; rituximab; prospective study; sensitivity and specificity; metastasis; progression free survival; mantle cell lymphoma; multiple cycle treatment; maintenance therapy; cohort analysis; cyclophosphamide; molecular marker; cancer regression; minimal residual disease; real time polymerase chain reaction; predictive value; clinical outcome; cancer prognosis; consolidation chemotherapy; very elderly; human; male; female; cyclophosphamide plus doxorubicin plus prednisolone plus rituximab plus vincristine
Journal Title: Journal of Clinical Oncology
Volume: 42
Issue: 5
ISSN: 0732-183X
Publisher: American Society of Clinical Oncology  
Date Published: 2024-02-10
Start Page: 538
End Page: 549
Language: English
DOI: 10.1200/jco.23.00899
PROVIDER: scopus
PUBMED: 37992261
DOI/URL:
Notes: Source: Scopus
Altmetric
Citation Impact
BMJ Impact Analytics
MSK Authors
  1. Gilles Andre Salles
    272 Salles