Subcutaneous Rituximab-MiniCHOP Compared With Subcutaneous Rituximab-MiniCHOP Plus Lenalidomide in Diffuse Large B-Cell Lymphoma for Patients Age 80 Years or Older

Author:

Oberic Lucie1,Peyrade Frederic2,Puyade Mathieu3,Bonnet Christophe4,Dartigues-Cuillères Peggy5,Fabiani Bettina6,Ruminy Philippe7,Maisonneuve Hervé8,Abraham Julie9,Thieblemont Catherine10ORCID,Feugier Pierre11,Salles Gilles12ORCID,Bijou Fontanet13ORCID,Pica Gian-Matteo14,Damaj Gandhi15ORCID,Haioun Corinne16,Casasnovas René-Olivier17ORCID,Farhat Hassan18,Le Calloch Ronan19ORCID,Waultier-Rascalou Agathe20,Malak Sandra21,Paget Jerome22ORCID,Gat Elodie22,Tilly Hervé23,Jardin Fabrice23ORCID

Affiliation:

1. Department of Hematology, Institut Universitaire du Cancer, Toulouse-Oncopole, Toulouse, France

2. Department of Medical Oncology, Centre Antoine Lacassagne, Nice, France

3. Department of Oncology-Haematology and Cell Therapy, CHU, Poitiers, INSERM, Inserm CIC 1402, Poitiers, France

4. Clinical Hematology Unit, CHU Liège, Liège Université, Campus Universitaire de Sart Tilman, Liège, Belgique

5. Anapath Research Unit (EA) EA4340 and Pathology Laboratory, Versailles University and APHP, Ambroise Paré Hospital, Boulogne, France

6. Department of Pathology, Hopital Saint-Antoine, APHP, Paris, France

7. INSERM U1245, Centre Henri Becquerel, Rouen, France

8. Department of Clinical Hematology, Centre Hospitalier Départemental Vendée, La Roche-sur-Yon, France

9. Department of Hematology, CHU Dupuytren, Limoges, France

10. APHP, Hopital Saint-Louis, Hemato-oncologie; Université de Paris, Paris Diderot, Paris, France

11. Department of Haematology, Centre Hospitalier Régional Universitaire de Nancy, Vandoeuvre Les Nancy, France

12. Department of Hematology, Centre Hospitalier Lyon Sud, Hospices Civils de Lyon, Pierre Benite, France

13. Department of Hematology, Hospital Bergonié, Bordeaux, France

14. Department of Hematology, Centre Hospitalier Métropole Savoie, Chambery, France

15. Department of Hematology, CHU Caen, Caen, France

16. Department of Hematology, Henri Mondor University Hospital, UPEC, Creteil, France

17. Department of Hematology and INSERM1231, CHU Dijon Bourgogne, Dijon, France

18. Department of Hematology, Centre Hospitalier de Versailles André Mignot, Versailles, France

19. Centre hospitalier de Quimper Cornouaille/Université de Bretagne Occidentale, France

20. Department of Hematology, Centre Hospitalier Universitaire Nimes Caremeau, Nîmes, France

21. Department of Hematology, CLCC Rene Huguenin Institut Curie, Saint-Cloud, France

22. LYSARC, The Lymphoma Academic Research Organisation, Centre Hospitalier Lyon-Sud, Pierre-Bénite, France

23. Department of Hematology, Centre Henri Becquerel, UNIROUEN, University of Normandy, INSERM U1245, Rouen, France

Abstract

PURPOSE: The prognosis of elderly patients with diffuse large B-cell lymphoma (DLBCL) is worse than that of young patients. An attenuated dose of chemotherapy—cyclophosphamide, doxorubicin, vincristine, and prednisone plus rituximab (R-miniCHOP)—is a good compromise between efficacy and safety in very elderly patients. In combination with R-CHOP (R2-CHOP), lenalidomide has an acceptable level of toxicity and may mitigate the negative prognosis of the non–germinal center B-cell–like phenotype. The Lymphoma Study association conducted a multicentric, phase III, open-label, randomized trial to compare R-miniCHOP and R2-miniCHOP. PATIENTS AND METHODS: Patients of age 80 years or older with untreated DLBCL were randomly assigned into the R-miniCHOP21 group or the R2-miniCHOP21 group for six cycles and stratified according to CD10 expression and age. The first cycle of rituximab was delivered by IV on D1 after a prephase and then delivered subcutaneously on D1 of cycles 2-6. Lenalidomide was delivered at a dose of 10 mg once daily on D1-D14 of each cycle. The primary end point was overall survival (OS). RESULTS: A total of 249 patients with new DLBCL were randomly assigned (127 R-miniCHOP and 122 R2-miniCHOP). The median age was 83 years (range, 80-96), and 55% of the patients were classified as non-GCB. The delivered dose for each R-miniCHOP compound was similar in both arms. Over a median follow-up of 25.1 months, the intention-to-treat analysis revealed that R2-miniCHOP did not improve OS (2-year OS 66% in R-miniCHOP and 65.7% in R2-miniCHOP arm, P = .98) in the overall population or in the non-GCB population. Grade 3-4 adverse events occurred in 53% of patients with R-miniCHOP and in 81% of patients with R2-miniCHOP. CONCLUSION: The addition of lenalidomide to R-miniCHOP does not improve OS. Rituximab delivered subcutaneously was safe in this population.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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