Clinicopathological features and survival in EBV-positive diffuse large B-cell lymphoma not otherwise specified

Author:

Bourbon Estelle12,Maucort-Boulch Delphine234ORCID,Fontaine Juliette5,Mauduit Claire5,Sesques Pierre1,Safar Violaine1,Ferrant Emmanuelle1,Golfier Camille1,Ghergus Dana1,Karlin Lionel1,Lazareth Anne1,Bouafia Fadhela1ORCID,Pica Gian Matteo6,Orsini-Piocelle Frédérique7,Rocher Clément8,Gros François-Xavier9ORCID,Parrens Marie1011,Dony Arthur12,Rossi Cédric1314ORCID,Ghesquières Hervé1215,Bachy Emmanuel1215ORCID,Traverse-Glehen Alexandra2515,Sarkozy Clémentine16

Affiliation:

1. Service d’Hématologie, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, Pierre Bénite Cedex, France;

2. Université de Lyon, Université Claude Bernard Lyon 1, Villeurbanne, France;

3. Service de Biostatistique et Bioinformatique, Pôle Santé Publique, Hospices Civils de Lyon, Lyon, France;

4. Centre national de la recherche scientifique (CNRS), Unité Mixte de Recherche (UMR) 5558, Laboratoire de Biométrie et Biologie Évolutive, Équipe Biostatistique-Santé, Villeurbanne, France;

5. Service d’Anatomie Pathologique, Centre Hospitalier Lyon-Sud, Hospices Civils de Lyon, Pierre Bénite Cedex, France;

6. Service d’Hématologie, Centre hospitalier Métropole Savoie, Chambéry, France;

7. Service d’Hématologie, Hôpital Annecy-Genevois, Annecy, France;

8. Service d’Hématologie, Groupement Hospitalier Nord Dauphiné, Bourgoin Jallieu, France;

9. Service d’Hématologie clinique et de Thérapies cellulaires and

10. Service d’Anatomie et de Pathologie, Centre Hospitalo-Universitaire de Bordeaux, Bordeaux, France;

11. INSERM U1053, BaRITOn, Université de Bordeaux, Bordeaux, France;

12. Service d’Hématologie, Hôpital Nord-Ouest, Villefranche-sur-Saône, France;

13. Service d’Hématologie, Centre Hospitalier Universitaire de Dijon, Dijon, France;

14. INSERM UMR 1231, Dijon, France;

15. EA LIB (Lymphoma ImmunoBiology), Université Claude Bernard Lyon 1, Lyon, France; and

16. Département d’Innovation thérapeutique, Institut Gustave Roussy, Villejuif, France

Abstract

Abstract In this retrospective study, we report 70 cases of Epstein-Barr virus (EBV)+ diffuse large B-cell lymphoma not otherwise specified (DLBCL-NOS) among 1696 DLBCL-NOS cases diagnosed between 2006 and 2019 (prevalence of 4.1%). At diagnosis, median age was 68.5 years; 79% of the cases presented with an advanced-stage disease (III-IV), 48% with extranodal lesions, and 14% with an hemophagocytic lymphohistiocytosis (HLH) (8 at diagnosis and 1 on therapy). A total of 46 cases presented a polymorphic pattern, and 21 were monomorphic. All had a non-germinal center B phenotype, with the majority of tumor cells expressing CD30 and programmed death ligand 1 (98% and 95%, respectively). Type II and III EBV latency was seen in 88% and 12% of the cases, respectively. Patients were treated with immunochemotherapy (59%) or chemotherapy (22%), and 19% received palliative care due to advanced age and altered performance status. After a median follow-up of 48 months, progression-free survival (PFS) and overall survival (OS) at 5 years were 52.7% and 54.8%, respectively. Older age (>50 years) and HLH were associated with shorter PFS and OS in multivariate analysis (PFS: hazard ratio [HR], 14.01; 95% confidence interval [CI], 2.34-83.97; and HR, 5.78; 95% CI, 2.35-14.23; OS: HR, 12.41; 95% CI, 1.65-93.53; and HR, 6.09; 95% CI, 2.42-15.30, respectively). Finally, using a control cohort of 425 EBV− DLBCL-NOS, EBV positivity was associated with a shorter OS outcome within patients >50 years (5-year OS, 53% [95% CI, 38.2-74] vs 60.8% [95% CI, 55.4-69.3], P = .038), but not in younger patients.

Publisher

American Society of Hematology

Subject

Hematology

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