Outcomes after first-line immunochemotherapy for primary mediastinal B-cell lymphoma: a LYSA study

Author:

Camus Vincent1,Rossi Cédric2ORCID,Sesques Pierre3,Lequesne Justine4,Tonnelet David5ORCID,Haioun Corinne6,Durot Eric7ORCID,Willaume Alexandre8,Gauthier Martin9ORCID,Moles-Moreau Marie-Pierre10,Antier Chloé11,Lazarovici Julien12,Monjanel Hélène1314,Bernard Sophie15,Tardy Magalie16,Besson Caroline17ORCID,Lebras Laure18,Choquet Sylvain19,Le Du Katell20ORCID,Bonnet Christophe21,Bailly Sarah22,Damaj Ghandi23ORCID,Laribi Kamel24,Maisonneuve Hervé25,Houot Roch26,Chauchet Adrien27,Jardin Fabrice1,Traverse-Glehen Alexandra28,Decazes Pierre5ORCID,Becker Stéphanie5,Berriolo-Riedinger Alina29ORCID,Tilly Hervé1

Affiliation:

1. Department of Hematology and INSERM U1245, Centre Henri Becquerel, Rouen, France;

2. Department of Hematology, University Hospital, Dijon, France;

3. Department of Hematology, Hospices Civils de Lyon, Pierre-Bénite, France;

4. Clinical Research Unit, Centre Henri Becquerel, Rouen, France;

5. Department of Nuclear Medicine and QUANTIF-LITIS, Centre Henri Becquerel, Rouen, France;

6. Lymphoid Malignancies Unit, Henri Mondor University Hospital, Assistance Publique Hôpitaux de Paris, Créteil, France;

7. Department of Hematology, CHU de Reims, Reims, France;

8. Department of Hematology, Lille University Hospital–Hopital Claude Hurriez, Lille, France;

9. Department of Hematology, IUCT Oncopole, Toulouse, France;

10. Department of Hematology, Angers University Hospital, Angers, France;

11. Department of Hematology, University Hospital, Nantes, France;

12. Department of Hematology, Institut Gustave Roussy, Villejuif, France;

13. Department of Hematology, CH Aurillac, Aurillac, France;

14. Department of Hematology, Clermont-Ferrand University Hospital, Clermont-Ferrand, France;

15. Department of Hematology, CHU Saint Louis, Paris, France;

16. Department of Hematology, Centre Antoine Lacassagne, Nice, France;

17. Service d’Hémato-oncologie, Centre Hospitalier de Versailles, Le Chesnay, France;

18. Department of Hematology, Centre Léon Bérard, Lyon, France;

19. Department of Hematology, CHU La Pitié Salpetriere, Paris, France;

20. Department of Hematology, Clinique Victor Hugo, Le Mans, France;

21. Department of Hematology, Liege University Hospital, Liege, Belgique;

22. Department of Hematology, Cliniques Universitaires Saint Luc, Brussels, Belgium;

23. Department of Hematology, Côte de Nacre University Hospital, Caen, France;

24. Department of Hematology, CH Le Mans, Le Mans, France;

25. Department of Hematology, CH Départemental de Vendée, La-Roche-Sur-Yon, France;

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

27. Department of Hematology, CH Besançon, Besançon, France;

28. Department of Pathology, Hospices Civils de Lyon, Centre Hospitalier Lyon-Sud, UMR CNRS 5239, Pierre-Bénite, France; and

29. Department of Nuclear Medicine, University Hospital, Dijon, France

Abstract

Abstract Primary mediastinal B-cell lymphoma (PMBL) is a rare type of aggressive lymphoma typically affecting young female patients. The first-line standard of care remains debated. We performed a large multicenter retrospective study in 25 centers in France and Belgium to describe PMBL patient outcomes after first-line treatment in real-life settings. A total of 313 patients were enrolled and received rituximab (R) plus ACVBP (doxorubicin, cyclophosphamide, vindesine, bleomycin, and prednisone) (n = 180) or CHOP (cyclophosphamide, doxorubicin, vincristine, and prednisone) delivered every 14 days (R-CHOP14, n = 76) or 21 days (R-CHOP21, n = 57) and consolidation strategies in modalities that varied according to time and institution, mainly guided by positron emission tomography. Consolidation autologous stem cell transplantation was performed for 46 (25.6%), 24 (31.6%), and 1 (1.8%) patient in the R-ACVBP, R-CHOP14, and R-CHOP21 groups, respectively (P < .001); only 17 (5.4%) patients received mediastinal radiotherapy. The end-of-treatment complete metabolic response rates were 86.3%, 86.8%, and 76.6% (P = .23) in the R-ACVBP, R-CHOP14, and R-CHOP21 groups. The median follow-up was 44 months, and the R-ACVBP, R-CHOP14, and R-CHOP21 three-year progression-free survival probabilities were 89.4% (95% confidence interval [CI], 84.8-94.2), 89.4% (95% CI, 82.7-96.6), and 74.7% (95% CI, 64-87.1) (P = .018). A baseline total metabolic tumor volume (TMTV) ≥360 cm3 was associated with a lower progression-free survival (hazard ratio, 2.18; 95% CI, 1.05-4.53). Excess febrile neutropenia (24.4% vs 5.3% vs 5.3%; P < .001) and mucositis (22.8% vs 3.9% vs 1.8%; P < .001) were observed with R-ACVBP compared with the R-CHOP regimens. Patients with PMBL treated with dose-dense immunochemotherapy without radiotherapy have excellent outcomes. R-ACVBP acute toxicity was higher than that of R-CHOP14. Our data confirmed the prognostic importance of baseline TMTV.

Publisher

American Society of Hematology

Subject

Hematology

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