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

Journal of clinical oncology : official journal of the American Society of Clinical Oncology
ISSN: 1527-7755
Titre abrégé: J Clin Oncol
Pays: United States
ID NLM: 8309333

Informations de publication

Date de publication:
22 Nov 2023
Historique:
medline: 22 11 2023
pubmed: 22 11 2023
entrez: 22 11 2023
Statut: aheadofprint

Résumé

The 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. Previously 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. A qPCR assay with a median sensitivity of 1 × 10 The 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.

Identifiants

pubmed: 37992261
doi: 10.1200/JCO.23.00899
doi:

Banques de données

ClinicalTrials.gov
['NCT00209209']

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

JCO2300899

Auteurs

Eva Hoster (E)

Institute for Medical Informatics, Biometry, and Epidemiology (IBE), LMU Munich, Munich, Germany.
Department of Internal Medicine III, University Hospital LMU Munich, Munich, Germany.

Marie-Hélène Delfau-Larue (MH)

Department of Immunobiology and Inserm U955, Université Hôpital Henri Mondor, Créteil, France.

Elizabeth Macintyre (E)

Laboratory of Onco-Hematology, Université Paris Cité, Institut Necker-Enfants Malades and Assistance Publique-Hôpitaux de Paris, Paris, France.

Linmiao Jiang (L)

Institute for Medical Informatics, Biometry, and Epidemiology (IBE), LMU Munich, Munich, Germany.

Stephan Stilgenbauer (S)

Department of Internal Medicine III, University of Ulm, Ulm, Germany.

Ursula Vehling-Kaiser (U)

VK&K Studien GbR, Landshut, Germany.

Gilles Salles (G)

Hospices Civils de Lyon, Université Claude Bernard, Centre Hospitalier Lyon-Sud, Pierre Bénite, France.
Department of Medicine, Memorial Sloan Kettering Cancer Center, New York, NY.

Catherine Thieblemont (C)

Department of Hematology, Hôpital Saint Louis, Paris, France.

Hervé Tilly (H)

Department of Hematology and U1245, Centre Henri Becquerel, Rouen, France.

Stefan Wirths (S)

Department of Medicine II, University of Tübingen, Tübingen, Germany.

Pierre Feugier (P)

Department of Hematology and INSERM 1256, University of Lorraine, Vandoeuvre les Nancy, France.

Kai Hübel (K)

Klinik I für Innere Medizin, Universität zu Köln, Köln, Germany.

Christian Schmidt (C)

Department of Internal Medicine III, University Hospital LMU Munich, Munich, Germany.

Vincent Ribrag (V)

Institut Gustave Roussy, Villejuif, France.

Johanna C Kluin-Nelemans (JC)

Department of Hematology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.

Martin Dreyling (M)

Department of Internal Medicine III, University Hospital LMU Munich, Munich, Germany.

Christiane Pott (C)

Department of Medicine, University Hospital Schleswig-Holstein Campus Kiel/Christian-Albrechts University Kiel, Germany.

Classifications MeSH