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Obinutuzumab plus lenalidomide in advanced, previously untreated follicular lymphoma in need of systemic therapy: a LYSA study.
Bachy, Emmanuel; Houot, Roch; Feugier, Pierre; Bouabdallah, Krimo; Bouabdallah, Reda; Virelizier, Emmanuelle Nicolas; Maerevoet, Marie; Fruchart, Christophe; Snauwaert, Sylvia; Le Gouill, Steven; Marolleau, Jean-Pierre; Molina, Lysiane; Moluçon-Chabrot, Cécile; Thieblemont, Catherine; Tilly, Hervé; Bijou, Fontanet; Haioun, Corinne; Van den Neste, Eric; Fabiani, Bettina; Meignan, Michel; Cartron, Guillaume; Salles, Gilles; Casasnovas, Olivier; Morschhauser, Franck.
Afiliación
  • Bachy E; Hematology Department, Hospices Civils de Lyon, Lyon 1 Claude Bernard University, Lyon, France.
  • Houot R; Hematology Department, CHU Rennes, Rennes, France.
  • Feugier P; Hematology Department, CHU Nancy, France and Lorraine University, Nancy, France.
  • Bouabdallah K; Hematology Department, CHU Bordeaux, Pessac, France.
  • Bouabdallah R; Hematology Department, Institut Paoli Calmette, Marseille, France.
  • Virelizier EN; Hematology Department, Centre Léon Bérard, Lyon, France.
  • Maerevoet M; Hematology Department, Institut Bordet, Brussels, Belgium.
  • Fruchart C; Hematology Department, CH Dunkerque, Dunkirk, France.
  • Snauwaert S; Hematology Department, AZ Sint-Jan Brugge, Bruges, Belgium.
  • Le Gouill S; Hematology Department, CHU Nantes, Nantes, France.
  • Marolleau JP; Hematology Department, CHU Amiens, Amiens, France.
  • Molina L; Hematology Department, CHU Grenoble, Grenoble, France.
  • Moluçon-Chabrot C; Hematology Department, CHU Estaing, Clermont-Ferrand, France.
  • Thieblemont C; Hematology Department, Hôpital Saint Louis, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
  • Tilly H; Department of Hematology and U1245, Centre Henri Becquerel, Université de Rouen, Rouen, France.
  • Bijou F; Hematology Department, Institut Bergonnié, Bordeaux, France.
  • Haioun C; Lymphoid Malignancy Unit, Hôpital Henri Mondor, AP-HP, Créteil, France.
  • Van den Neste E; Cliniques Universitaires UCL Saint-Luc, Louvain, Belgium.
  • Fabiani B; Pathology Department, CHU Saint-Antoine, AP-HP, Paris, France.
  • Meignan M; Nuclear Medicine Department, CHU Henri Mondor, Cretéil, France.
  • Cartron G; Hematology Department, CHU Montpellier, Montpellier, France.
  • Salles G; Hematology Department, Hospices Civils de Lyon, Lyon 1 Claude Bernard University, Lyon, France.
  • Casasnovas O; Hematology Department, CHU Dijon, Dijon, France; and.
  • Morschhauser F; Hematology Department, CHU Lille, Lille, France.
Blood ; 139(15): 2338-2346, 2022 04 14.
Article en En | MEDLINE | ID: mdl-34936697
Obinutuzumab and lenalidomide (referred to as the GALEN combination) is an active immunomodulatory combination with a manageable safety profile in multiple types of lymphoma. We report efficacy and safety results for the phase 2 GALEN study in previously untreated patients with advanced follicular lymphoma (FL). Eligible patients aged ≥18 years had an Eastern Cooperative Oncology Group performance status ≤2 and high-tumor burden, grade 1 to 3a FL. Induction treatment was obinutuzumab (1000 mg IV, days 8, 15, and 22, cycle 1; day 1, cycles 2-6) plus lenalidomide (20 mg/d, days 1-21, cycle 1; days 2-22, cycles 2-6) for six 28-day cycles. Maintenance included obinutuzumab (1000 mg every 2 cycles) plus lenalidomide (10 mg, days 2-22) for ≤12 cycles (year 1) followed by obinutuzumab (1000 mg every 56 days) for 6 cycles (year 2). The primary end point was complete response rate (CRR) after induction per the 1999 International Working Group criteria. From October 2015 to February 2017, a total of 100 patients were enrolled. CRR after induction was 47%, and the overall response rate (ORR) was 92%. Post hoc analyses per the 2014 Lugano classification, including patients with missing bone marrow assessments, identified an additional 13 patients fulfilling CRR criteria, resulting in a complete metabolic response of 80% and an ORR of 94%. At a median follow-up of 3.7 years, 3-year progression-free survival and overall survival were 82% and 94%, respectively. The most common adverse event was neutropenia (48% any grade; 47% grade ≥3). Only 2% of patients presented with febrile neutropenia; others were mainly grade ≤2. No other specific grade ≥3 toxicity occurred at a frequency >3%. Overall, these results showed promising clinical efficacy for the chemotherapy-free GALEN backbone in previously untreated patients with high tumor burden FL. Except for neutropenia, the safety profile of the combination is remarkable. The study was registered at clinicaltrials.gov as #NCT01582776.
Asunto(s)

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Linfoma Folicular / Neutropenia Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Humans Idioma: En Revista: Blood Año: 2022 Tipo del documento: Article País de afiliación: Francia

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Linfoma Folicular / Neutropenia Tipo de estudio: Prognostic_studies Límite: Adolescent / Adult / Humans Idioma: En Revista: Blood Año: 2022 Tipo del documento: Article País de afiliación: Francia