Obinutuzumab versus Rituximab in transplant-eligible Mantle cell lymphoma patients.


Journal

Blood
ISSN: 1528-0020
Titre abrégé: Blood
Pays: United States
ID NLM: 7603509

Informations de publication

Date de publication:
26 Apr 2024
Historique:
accepted: 18 03 2024
received: 12 01 2024
revised: 01 03 2024
medline: 26 4 2024
pubmed: 26 4 2024
entrez: 26 4 2024
Statut: aheadofprint

Résumé

Obinutuzumab (O) and Rituximab (R) are two CD antibodies that have never been compared in a prospective randomised trial in mantle cell lymphoma (MCL). Herein, we report the long-term outcome of the LYMA-101 (NCT02896582) trial, in which newly diagnosed MCL patients were treated with chemotherapy plus O before transplantation followed by O maintenance (O group). We then compared these patients to those treated with the same treatment design with Rituximab instead of O (R group) (NCT00921414). A propensity score matching (PSM) was used to compare the two populations (O vs R groups) in terms of MRD at the end of induction (EOI), PFS and OS. In LYMA-101, the estimated five-year PFS and OS since inclusion (n=85) were 83.4% (95%CI: 73.5-89.8%) and 86.9% (95%CI: 77.6-92.5%), respectively. At EOI, patients treated in the O group had more frequent bone marrow MRD negativity than those treated in the R group (83.1% vs 63.4% Chi2 p=0.007). The PSM resulted in 2 sets of 82 patients with comparable characteristics at inclusion. From treatment initiation, the O group had a longer estimated five-year PFS (p=0.029; 82.8% versus 66.6%, HR 1.99, IC95 1.05-3.76) and OS (p=0.039; 86.4% versus 71.4% (HR 2.08, IC95 1.01-4.16) compared to the R group. Causes of death were comparable in the 2 groups, the most common cause being lymphoma. Obinutuzumab prior to transplantation and in maintenance provides better disease control and enhances PFS and OS, as compared to Rituximab in transplant-eligible MCL patients.

Identifiants

pubmed: 38669626
pii: 515910
doi: 10.1182/blood.2024023944
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright © 2024 American Society of Hematology.

Auteurs

Clémentine Sarkozy (C)

Institut Curie, Hematology department, Saint Cloud, France.

Mary Bridgid Callanan (MB)

University of Burgundy-INSERM 1231-CHU Dijon, DIJON, France.

Catherine Thieblemont (C)

AP-HP, Hôpital Saint-Louis, Hemato-oncologie, DMU DHI,F-75010 Paris, France, Paris, France.

Lucie Obéric (L)

Department of Hematology, Institut universitaire du cancer Toulouse- Oncopole, Toulouse, France.

Barbara Burroni (B)

Cochin Hospital, Assistance Publique des Hôpitaux de Paris, Paris, France.

Krimo Bouabdallah (K)

CHU de Bordeaux, France.

Ghandi Damaj (G)

Normandy University, Hematology Institute, Caen, France.

Benoit Tessoulin (B)

Nantes University Hospital, Nantes, France.

Vincent Ribrag (V)

Institut Gustave Roussy, Villejuif, France.

Roch Huout (R)

CHU Rennes, University of Rennes, Rennes, France.

Franck Morschhauser (F)

University of Lille, Lille, France.

Samuel Griolet (S)

LYSARC, Statistics, Pierre-Benite, Pierre-Bénite, France.

Clémentine Joubert (C)

Lymphoma Academic Research Organisation, Lyon, France.

Victoria Cacheux (V)

Clermont-Ferrand Univeristy Hospital, Clermont-Ferrand, France.

Vincent Delwail (V)

chu, 86021, France.

Violaine Safar (V)

Hospices Civils de Lyon, Pierre-Bénite, France.

Remy Gressin (R)

chu michallon, GRENOBLE, France.

Morgane Cheminant (M)

Hôpital Necker, APHP, paris, France.

Marie-Helene Delfau-Larue (MH)

APHP, GH MONDOR, UPEC university, INSERM U955, CRETEIL, France.

Olivier Hermine (O)

INSERM U1163 CNRS ERL8254 Imagine Institute, Paris, France.

Elizabeth A Macintyre (EA)

Hopital Necker, Université de Paris, Paris, France.

Steven Le Gouill (S)

Institut Curie, Paris, France.

Classifications MeSH