Integrative analysis of a phase 2 trial combining lenalidomide with CHOP in angioimmunoblastic T-cell lymphoma.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
26 01 2021
Historique:
received: 29 07 2020
accepted: 02 12 2020
entrez: 26 1 2021
pubmed: 27 1 2021
medline: 15 5 2021
Statut: ppublish

Résumé

Angioimmunoblastic T-cell lymphoma (AITL) is a frequent T-cell lymphoma in the elderly population that has a poor prognosis when treated with cyclophosphamide, doxorubicin, vincristine, and prednisone  (CHOP) therapy. Lenalidomide, which has been safely combined with CHOP to treat B-cell lymphoma, has shown efficacy as a single agent in AITL treatment. We performed a multicentric phase 2 trial combining 25 mg lenalidomide daily for 14 days per cycle with 8 cycles of CHOP21 in previously untreated AITL patients aged 60 to 80 years. The primary objective was the complete metabolic response (CMR) rate at the end of treatment. Seventy-eight of the 80 patients enrolled were included in the efficacy and safety analysis. CMR was achieved in 32 (41%; 95% confidence interval [CI], 30%-52.7%) patients, which was below the prespecified CMR rate of 55% defined as success in the study. The 2-year progression-free survival (PFS) was 42.1% (95% CI, 30.9%-52.8%), and the 2-year overall survival was 59.2% (95% CI, 47.3%-69.3%). The most common toxicities were hematologic and led to treatment discontinuation in 15% of patients. This large prospective and uniform series of AITL treatment data was used to perform an integrative analysis of clinical, pathologic, biologic, and molecular data. TET2, RHOA, DNMT3A, and IDH2 mutations were present in 78%, 54%, 32%, and 22% of patients, respectively. IDH2 mutations were associated with distinct pathologic and clinical features and DNMT3A was associated with shorter PFS. In conclusion, the combination of lenalidomide and CHOP did not improve the CMR in AITL patients. This trial clarified the clinical impact of recurrent mutations in AITL. This trial was registered at www.clincialtrials.gov as #NCT01553786.

Identifiants

pubmed: 33496747
pii: S2473-9529(21)00068-9
doi: 10.1182/bloodadvances.2020003081
pmc: PMC7839364
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
Lenalidomide F0P408N6V4

Banques de données

ClinicalTrials.gov
['NCT01553786']

Types de publication

Clinical Trial, Phase II Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

539-548

Informations de copyright

© 2021 by The American Society of Hematology.

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Auteurs

François Lemonnier (F)

Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpitaux Universitaires Henri Mondor, Unité Hémopathies Lymphoïdes, Créteil, France.
Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.

Violaine Safar (V)

Service d'Hématologie Clinique, Hospices Civils de Lyon, Pierre-Bénite, and Université Lyon 1, Lyon, France.

Asma Beldi-Ferchiou (A)

Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.
Département d'Hématologie et d'Immunologie Biologique, Hôpitaux Universitaires Henri Mondor, AP-HP, Créteil, France.

Anne-Ségolène Cottereau (AS)

Département de Médecine Nucléaire, Hôpital Cochin, AP-HP, Université Paris Descartes, Paris, France.

Emmanuel Bachy (E)

Service d'Hématologie Clinique, Hospices Civils de Lyon, Pierre-Bénite, and Université Lyon 1, Lyon, France.

Guillaume Cartron (G)

Département d'Hématologie Clinique, Centre Hospitalo-Universitaire de Montpellier, Unité Mixte de Recherche-Centre National de Recherche Scientifique 5535, Université de Montpellier, Montpellier, France.

Virginie Fataccioli (V)

Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.
Département de Pathologie, Hôpitaux Universitaires Henri Mondor, Créteil, France.

Laura Pelletier (L)

Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.

Cyrielle Robe (C)

Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.
Département de Pathologie, Hôpitaux Universitaires Henri Mondor, Créteil, France.

Audrey Letourneau (A)

Institut de Pathologie, Centre Hospitalier Universitaire Vaudois et Université de Lausanne, Lausanne, Switzerland.

Edoardo Missiaglia (E)

Institut de Pathologie, Centre Hospitalier Universitaire Vaudois et Université de Lausanne, Lausanne, Switzerland.

Slim Fourati (S)

Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.
Service de Virologie, Département Prévention, Diagnostic et Traitement des Infections, Hôpitaux Universitaires Henri Mondor, AP-HP, Créteil, France.

Marie-Pierre Moles-Moreau (MP)

Service d'Hématologie, Centre Hospitalier Universitaire, Angers, France.

Alain Delmer (A)

Service d'Hématologie, Centre Hospitalier Universitaire, Reims, France.

Reda Bouabdallah (R)

Service d'Hématologie, Institut Paoli-Calmette, Marseille, France.

Laurent Voillat (L)

Service d'Hématologie, Centre Hospitalier, Chalon, France.

Stéphanie Becker (S)

Service de Médecine Nucléaire, Centre de Lutte Contre le Cancer Becquerel, Rouen, France.

Céline Bossard (C)

Université de Nantes, Center Hospitalier Universitaire Nantes, Département de Pathologie, INSERM Centre de Recherche en Cancérologie et Immunologie Nantes Angers, Nantes, France.

Marie Parrens (M)

Département de Pathologie, Hôpital Haut-Lévêque, Pessac, INSERM U1053, Université de Bordeaux, Bordeaux, France.

Olivier Casasnovas (O)

Service d'Hématologie, Centre Hospitalier Universitaire, Dijon, France.

Victoria Cacheux (V)

Service d'Hématologie, Centre Hospitalier Universitaire, Clermont Ferrand, France.

Caroline Régny (C)

Service d'Hématologie, Centre Hospitalier Universitaire, Grenoble, France.

Vincent Camus (V)

Département d'Hématologie, Centre Henri Becquerel, Rouen, France; and.

Marie-Hélène Delfau-Larue (MH)

Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.
Département d'Hématologie et d'Immunologie Biologique, Hôpitaux Universitaires Henri Mondor, AP-HP, Créteil, France.

Michel Meignan (M)

LYSA Image, Hôpitaux Universitaires Henri Mondor, Créteil, France.

Laurence de Leval (L)

Institut de Pathologie, Centre Hospitalier Universitaire Vaudois et Université de Lausanne, Lausanne, Switzerland.

Philippe Gaulard (P)

Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.
Département de Pathologie, Hôpitaux Universitaires Henri Mondor, Créteil, France.

Corinne Haioun (C)

Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpitaux Universitaires Henri Mondor, Unité Hémopathies Lymphoïdes, Créteil, France.
Université Paris Est Créteil, INSERM, Institut Médical de Recherche Biomédicale, Créteil, France.

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