Obinutuzumab vs rituximab for advanced DLBCL: a PET-guided and randomized phase 3 study by LYSA.


Journal

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

Informations de publication

Date de publication:
29 04 2021
Historique:
received: 19 08 2020
accepted: 09 11 2020
pubmed: 20 11 2020
medline: 15 12 2021
entrez: 19 11 2020
Statut: ppublish

Résumé

Rituximab plus polychemotherapy is the standard of care in diffuse large B-cell lymphoma (DLBCL). GAINED, a randomized phase 3 trial, compared obinutuzumab to rituximab. Transplant-eligible patients (18-60 years) with an untreated age-adjusted International Prognostic Index (aaIPI) score ≥1 DLBCL were randomized (1:1) between obinutuzumab or rituximab and stratified by aaIPI (1; 2-3) and chemotherapy regimen (doxorubicin, cyclophosphamide, prednisone plus vindesine, bleomycin [ACVBP] or vincristine [CHOP]). Consolidation treatment was determined according to response to interim positron emission tomography (PET). Responders after cycle 2 and 4 (PET2-/PET4-) received immunochemotherapy. Responders after only cycle 4 (PET2+/4-) received transplantation. The primary objective was an 8% improvement (hazard ratio [HR] = 0.73; 80% power; α risk, 2.5%; 1-sided) in 2-year event-free survival (EFS) in the obinutuzumab arm. From September 2012, 670 patients were enrolled (obinutuzumab, n = 336; rituximab, n = 334). A total of 383 (57.2%) were aaIPI 2-3, 339 (50.6%) received CHOP. Median follow-up was 38.7 months. The 2-year EFS was similar in both groups (59.8% vs 56.6%; P = .123; HR = 0.88). The 2-year PFS in the whole cohort was 83.1% (95% confidence interval, 80% to 85.8%). PET2-/4- and PET2+/4- had similar 2-year progression-free survival (PFS) and overall survival (OS): 89.9% vs 83.9% and 94.8% vs 92.8%. The 2-year PFS and OS for PET4+ patients were 62% and 83.1%. Grade 3-5 infections were more frequent in the obinutuzumab arm (21% vs 12%). Obinutuzumab is not superior to rituximab in aaIPI ≥1 DLBCL transplant-eligible patients. This trial was registered at www.clinicaltrials.gov as #NCT01659099.

Identifiants

pubmed: 33211799
pii: S0006-4971(21)00912-5
doi: 10.1182/blood.2020008750
doi:

Substances chimiques

Antibodies, Monoclonal, Humanized 0
Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
obinutuzumab O43472U9X8
Prednisone VB0R961HZT

Banques de données

ClinicalTrials.gov
['NCT01659099']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2307-2320

Commentaires et corrections

Type : CommentIn

Informations de copyright

© 2021 by The American Society of Hematology.

Auteurs

Steven Le Gouill (S)

Service d'Hématologie, Clinique du Centre Hospitalier Universitaire (CHU) de Nantes, Nantes, France.
Center for Research in Cancerology and Immunology Nantes/Angers (CRCINA), Nantes, France.
Nantes Excellence Trajectory (NeXT), Université de Nantes, INSERM, Nantes, France.

Hervé Ghesquières (H)

Department of Hematology, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, Université Claude Bernard Lyon 1, Pierre Bénite, Lyon, France.

Lucie Oberic (L)

Service d'Hématologie, Institut Universitaire du Cancer (IUC) Toulouse Oncopole, Toulouse, France.

Franck Morschhauser (F)

Department of Hematology, CHU Lille, Université de Lille, Lille, France.
Équipe d' Accueil (EA) 7365, Groupe de Recherche sur les Formes Injectables et les Technologies Associées (GRITA), Lille, France.

Hervé Tilly (H)

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

Vincent Ribrag (V)

Department of Hematology, Gustave Roussy, Université Paris-Saclay, Villejuif, France.

Thierry Lamy (T)

Department of Hematology, University Hospital of Rennes, Rennes, France.

Catherine Thieblemont (C)

Department of Hematology, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Université Paris Diderot, Paris, France.

Hervé Maisonneuve (H)

Department of Hematology, Hopital Departemental de Vendée, La Roche sur Yon, France.

Rémy Gressin (R)

Department of Hematology, CHU Grenoble, Grenoble, France.

Krimo Bouhabdallah (K)

Department of Hematology, University Hospital of Bordeaux, Bordeaux, France.

Corinne Haioun (C)

Department of Hematology, Hôpital H. Mondor, Creteil, France.

Gandhi Damaj (G)

Department of Hematology, Institut d'Hématologie de Basse Normandie, Caen, France.

Luc Fornecker (L)

Department of Hematology, University Hospital of Strasbourg, Strasbourg, France.

Réda Bouhabdallah (R)

Department of Hematology, Institut P. Calmette, Marseille, France.

Pierre Feugier (P)

Department of Hematology, University Hospital of Nancy, Vandoeuvre les Nancy, France.

David Sibon (D)

Department of Hematology, Hôpital Necker, Paris, France.

Guillaume Cartron (G)

Department of Hematology, University Hospital of Montpellier, Montpellier, France.

Christophe Bonnet (C)

Department of Hematology, CHU Liege, Liege, Belgium.

Marc André (M)

Department of Hematology, CHU Université Catholique de Louvain (UCL) Namur, Yvoir, Belgium.

Loic Chartier (L)

Department of Biostatistics, The Lymphoma Academic Research Organisation (LYSARC), Lyon, France.

Philippe Ruminy (P)

INSERM U1245, Centre Henri Becquerel, Rouen, France.

Françoise Kraeber-Bodéré (F)

Department of Nuclear Medicine, University Hospital of Nantes, Nantes, France.

Caroline Bodet-Milin (C)

Department of Nuclear Medicine, University Hospital of Nantes, Nantes, France.

Alina Berriolo-Riedinger (A)

Department of Nuclear Medicine, Centre Georges-François Leclerc, Dijon, France.

Josette Brière (J)

Department of Hematology, Hôpital Saint-Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Université Paris Diderot, Paris, France.

Jean-Philippe Jais (JP)

Department of Biostatistics, Hôpital Necker, University of Paris, Paris, France.
Institut Imagine, Unité INSERM 1163, Paris, France.

Thierry Jo Molina (TJ)

Institut Imagine, Unité INSERM 1163, Paris, France.
Department of Pathology, Hôpital Necker, University of Paris 3, Paris, France.

Emmanuel Itti (E)

Department of Nuclear Medicine, Hôpital H. Mondor, Creteil, France.

René-Olivier Casasnovas (RO)

Department of Hematology, University Hospital F. Mitterrand, Dijon, France; and.
Unité Mixte de Recherche (UMR) 1231, INSERM, Dijon, France.

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