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Obinutuzumab vs rituximab for transplant-eligible patients with mantle cell lymphoma.
Sarkozy, Clémentine; Callanan, Mary; Thieblemont, Catherine; Obéric, Lucie; Burroni, Barbara; Bouabdallah, Krimo; Damaj, Gandhi; Tessoulin, Benoit; Ribrag, Vincent; Houot, Roch; Morschhauser, Franck; Griolet, Samuel; Joubert, Clémentine; Cacheux, Victoria; Delwail, Vincent; Safar, Violaine; Gressin, Remy; Cheminant, Morgane; Delfau-Larue, Marie-Hélène; Hermine, Olivier; Macintyre, Elizabeth; Le Gouill, Steven.
Afiliação
  • Sarkozy C; Service d'hématologie, Institut Curie, Saint Cloud, France.
  • Callanan M; Université de Versailles Saint-Quentin, Versailles, France.
  • Thieblemont C; Laboratoire d'Imagerie Translationnelle en Oncologie, U1288 INSERM/Institut Curie Centre de Recherche, Paris, France.
  • Obéric L; University of Burgundy, INSERM U1231, Unit for Innovation in Genetics and Epigenetics in Oncology, University Hospital, Dijon, France.
  • Burroni B; Service d'Hématologie, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Bouabdallah K; Service d'Hématologie, Institut Universitaire du Cancer Toulouse, Oncopole, Toulouse, France.
  • Damaj G; Service d'Anatomopathologie, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, Paris, France.
  • Tessoulin B; Service d'Hématologie, Centre Hospitalier Universitaire de Bordeaux, Bordeaux, France.
  • Ribrag V; Service d'Hématologie, Centre Hospitalier Universitaire de Caen, Caen, France.
  • Houot R; Service d'Hématologie, Centre Hospitalier Universitaire Nantes, Nantes, France.
  • Morschhauser F; Département d'Hématologie, Institut Gustave Roussy, Villejuif, France.
  • Griolet S; Service d'Hématologie, Centre Hospitalier Universitaire Rennes, Rennes, France.
  • Joubert C; Department of Hematology, Claude Huriez Hospital, University of Lille, EA 7365, Research Group on Injectable Forms and Associated Technologies, Lille, France.
  • Cacheux V; LYSARC, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France.
  • Delwail V; LYSARC, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France.
  • Safar V; Service d'Hématologie, Centre Hospitalier Universitaire de Clermont-Ferrand, Clermont-Ferrand, France.
  • Gressin R; Service d'Hématologie, Hôpital Poitiers, Poitiers, France.
  • Cheminant M; Service d'Hématologie, Hôpital Lyon Sud, Pierre Bénite, France.
  • Delfau-Larue MH; Service d'Hématologie, Centre Hospitalier Universitaire Grenoble, Grenoble, France.
  • Hermine O; Department of Clinical Hematology, INSERM U1163, University of Paris, Necker University Hospital, Paris, France.
  • Macintyre E; Department of Immunology, INSERM U955 Équipe 9, Institut Mondor de Recherche Biomédicale, Hospital Henri Mondor, Creteil, France.
  • Le Gouill S; Department of Clinical Hematology, INSERM U1163, University of Paris, Necker University Hospital, Paris, France.
Blood ; 144(3): 262-271, 2024 Jul 18.
Article em En | MEDLINE | ID: mdl-38669626
ABSTRACT
ABSTRACT Obinutuzumab (O) and rituximab (R) are 2 CD antibodies that have never been compared in a prospective randomized trial of mantle cell lymphoma (MCL). Herein, we report the long-term outcome of the LyMa-101 trial, in which newly diagnosed patients with MCL were treated with chemotherapy plus O before transplantation, followed by O maintenance (O group). We then compared these patients with those treated with the same treatment design with R instead of O (R group). A propensity score matching (PSM) was used to compare the 2 populations (O vs R groups) in terms of measurable residual disease (MRD) at the end of induction (EOI), progression-free survival (PFS), and overall survival (OS). In LyMa-101, the estimated 5-year PFS and OS after inclusion (n = 85) were 83.4% (95% confidence interval [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%; χ2, P = .007). PSM resulted in 2 sets of 82 patients with comparable characteristics at inclusion. From treatment initiation, the O group had a longer estimated 5-year PFS (P = .029; 82.8% vs 66.6%; hazard ratio [HR], 1.99; 95% confidence interval (CI), 1.05-3.76) and OS (P = .039; 86.4% vs 71.4%; HR, 2.08; 95% CI, 1.01-4.16) compared with the R group. Causes of death were comparable in the 2 groups, the most common cause being lymphoma. O before transplantation and in maintenance provides better disease control and enhances PFS and OS compared with R in transplant-eligible patients with MCL. These trials were registered at www.clinicaltrials.gov as #NCT00921414 and NCT02896582.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma de Célula do Manto / Anticorpos Monoclonais Humanizados / Rituximab Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França País de publicação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Linfoma de Célula do Manto / Anticorpos Monoclonais Humanizados / Rituximab Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Revista: Blood Ano de publicação: 2024 Tipo de documento: Article País de afiliação: França País de publicação: Estados Unidos