Lenalidomide maintenance for diffuse large B-cell lymphoma patients responding to R-CHOP: quality of life, dosing, and safety results from the randomised controlled REMARC study.


Journal

British journal of haematology
ISSN: 1365-2141
Titre abrégé: Br J Haematol
Pays: England
ID NLM: 0372544

Informations de publication

Date de publication:
04 2020
Historique:
received: 02 04 2019
accepted: 13 09 2019
pubmed: 9 11 2019
medline: 24 11 2020
entrez: 9 11 2019
Statut: ppublish

Résumé

Lenalidomide maintenance therapy prolonged progression-free survival (PFS) versus placebo in elderly patients with diffuse large B-cell lymphoma (DLBCL) responding to induction chemotherapy in the phase 3 REMARC study. This subpopulation analysis assessed the impact of lenalidomide maintenance and treatment-emergent adverse events (TEAEs) on health-related quality of life (HRQOL). Global health status (GHS), and physical functioning and fatigue subscales were evaluated in patients who completed the European Organisation for Research and Treatment of Cancer quality-of-life questionnaire-C30 v3.0. The impact of TEAEs classified post hoc as subjective (patients can feel) or observable (only measurable by physicians) on dose reductions and discontinuations was assessed. Among 457 patients (lenalidomide, n = 229; placebo, n = 228), mean (standard deviation) GHS was similar between treatment arms [68·2 (20·7) Versus 72·0 (17·8)] at randomisation and remained similar during maintenance. Patients receiving lenalidomide experienced no meaningful changes in GHS, physical functioning, or fatigue. Observable TEAEs were more common (81·1% Versus 66·3%) and more likely to lead to dose reductions, than subjective TEAEs in both arms. PFS was superior in the lenalidomide arm regardless of dose reduction. Lenalidomide maintenance prolonged PFS and did not negatively impact HRQOL in patients with DLBCL despite TEAEs being more common, when compared with placebo.

Identifiants

pubmed: 31702836
doi: 10.1111/bjh.16300
pmc: PMC7154674
doi:

Substances chimiques

R-CHOP protocol 0
Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Lenalidomide F0P408N6V4
Prednisone VB0R961HZT

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

84-96

Subventions

Organisme : Celgene Corporation
Pays : International

Informations de copyright

© 2019 The Authors. British Journal of Haematology published by British Society for Haematology and John Wiley & Sons Ltd.

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Auteurs

Catherine Thieblemont (C)

Hemato-Oncology, APHP, Hôpital Saint-Louis, Paris, France.

Susannah Howlett (S)

Celgene Corporation, Summit, NJ, USA.

René-Olivier Casasnovas (RO)

Service d'Hématologie Clinique, Centre Hospitalier Universitaire de Dijon and INSERM UMR1231, Dijon, France.

Nicolas Mounier (N)

Hématologie, Centre Hospitalier Universitaire de Nice - Hôpital de l'Archet, Nice, France.

Aurore Perrot (A)

Service d'Hématologie, Centre Hospitalier Universitaire de Nancy, Nancy, France.

Franck Morschhauser (F)

Institute of Hematology-Transfusion, Centre Hospitalier Universitaire Régional de Lille, Lille, France.

Christophe Fruchart (C)

Service d'Hématologie, Institut d'Hématologie de Basse-Normandie, Centre Hospitalier Universitaire de Caen, Caen, France.

Nicolas Daguindau (N)

Service d'Hématologie Clinique, Centre Hospitalier Annecy Genevois, Annecy, France.

Koen van Eygen (K)

Oncologisch Centrum, AZ Groeninge Hospital, Kortrijk, Belgium.

Lucie Obéric (L)

Hôpital de Purpan, Centre Hospitalier Universitaire de Toulouse, Toulouse, France.

Reda Bouabdallah (R)

Department of Hematology, Institut Paoli Calmettes, Marseille, France.

Gian Matteo Pica (GM)

Centre Hospitalier de Metropole Savoie, Chambery, France.

Emmanuelle Nicolas-Virezelier (E)

Cancer Research Center of Lyon, Lyon, France.

Julie Abraham (J)

Centre Hospitalier Universitaire Dupuytren, Limoges, France.

Olivier Fitoussi (O)

Hematology/Oncology, Polyclinique Bordeaux Nord Aquitaine, Bordeaux, France.

Sylvia Snauwaert (S)

AZ Sint-Jan Brugge-Oostende, Bruges, Belgium.

Jean-Claude Eisenmann (JC)

Centre Hospitalier de Mulhouse, Mulhouse, France.

Pauline Lionne-Huyghe (P)

Centre Hospitalier d'Arras, Arras, France.

Dominique Bron (D)

Institut Jules Bordet, Brussels, Belgium.

Sabine Tricot (S)

Centre Hospitalier de Valenciennes, Valenciennes, France.

Dries Deeren (D)

AZ Delta, Roeselare, Belgium.

Hugo Gonzalez (H)

Centre Hospitalier René-Dubos, Pontoise, France.

Régis Costello (R)

Hôpital de la Conception, Marseille, France.

Katell Le Du (K)

Clinique Victor Hugo, Le Mans, France.

Maria Gomes da Silva (MG)

Instituto Português de Oncologia de Lisboa Francisco Gentil, Lisboa, Portugal.

Sebastian Grosicki (S)

Medical University of Silesia, Katowice, Poland.

Judith Trotman (J)

Concord Repatriation General Hospital, University of Sydney, Concord, NSW, Australia.

John Catalano (J)

Frankston Hospital and Monash University, Frankston, Vic., Australia.

Dolores Caballero (D)

Hospital Universitario de Salamanca, Salamanca, Spain.

Richard Greil (R)

Paracelsus Medical University Salzburg, Salzburg Cancer Research Institute, Salzburg, Austria.

Amos M Cohen (AM)

Rabin Medical Center, Beilinson Hospital, Davidoff Cancer Center, Tel Aviv University, Ramat Aviv, Tel Aviv, Israel.

Philippe Gaulard (P)

University Hospital Henri Mondor APHP, Créteil, France.

Louise Roulin (L)

Lymphoid Malignancies Unit, AP-HP, Groupe Hospitalier Mondor, Créteil, France.

Kenichi Takeshita (K)

Celgene Corporation, Summit, NJ, USA.

Marie-Laure Casadebaig (ML)

Celgene Corporation, Boudry, Switzerland.

Hervé Tilly (H)

Department of Hematology, Centre Henri Becquerel, UNIROUEN, INSERMU1245, Rouen, France.

Bertrand Coiffier (B)

Department of Hematology, INSERM U1052 Hospices Civils de Lyon, Pierre-Bénite, France.

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