Six-Year Results From RELEVANCE: Lenalidomide Plus Rituximab (R2) Versus Rituximab-Chemotherapy Followed by Rituximab Maintenance in Untreated Advanced Follicular Lymphoma

Author:

Morschhauser Franck1ORCID,Nastoupil Loretta2ORCID,Feugier Pierre3,Schiano de Colella Jean-Marc4ORCID,Tilly Hervé5,Palomba Maria Lia6ORCID,Bachy Emmanuel7ORCID,Fruchart Christophe8,Libby Edward N.9,Casasnovas Rene-Olivier10ORCID,Flinn Ian W.11ORCID,Haioun Corinne12,Maisonneuve Hervé13,Ysebaert Loic14ORCID,Bartlett Nancy L.15ORCID,Bouabdallah Kamal16,Brice Pauline17,Ribrag Vincent18,Le Gouill Steven19ORCID,Daguindau Nicolas20,Guidez Stéphanie21,Pica Gian Matteo22,García-Sancho Alejandro Martín23ORCID,López-Guillermo Armondo24ORCID,Larouche Jean-François25,Ando Kiyoshi26,Gomes da Silva Maria27ORCID,André Marc28,Kalung Wu29ORCID,Sehn Laurie H.30ORCID,Izutsu Koji31ORCID,Cartron Guillaume32ORCID,Gkasiamis Argyrios33,Crowe Russell33,Xerri Luc4,Fowler Nathan H.2,Salles Gilles6ORCID

Affiliation:

1. University of Lille, CHU Lille, Lille, France

2. The University of Texas MD Anderson Cancer Center, Houston, TX

3. Nancy University Hospital, Vandoeuvre-lès-Nancy, France

4. Institut Paoli Calmettes, CRCM, AMU, Marseille, France

5. Centre Henri Becquerel, Rouen, France

6. Memorial Sloan Kettering Cancer Center, New York, NY

7. Hospices Civils de Lyon and Claude Bernard Lyon 1 Université, Lyon, France

8. CH de Dunkerque, Dunkerque, France

9. University of Washington, Seattle, WA

10. CHU Dijon-Bourgogne, Dijon, France

11. Sarah Cannon Research Institute and Tennessee Oncology, Nashville, TN

12. Henri Mondor Université Hôpital, UPEC, Créteil, France

13. Centre Hospitalier Départemental Vendée, La Roche-sur-Yon, France

14. Institut Universitaire du Cancer Toulouse-Oncopole, Toulouse, France

15. Washington University School of Medicine, St Louis, MO

16. Bordeaux University Hospital, Bordeaux, France

17. Hôpital Saint-Louis, Paris, France

18. Institut Gustave Roussy, Villejuif, France

19. Institut Curie, Paris, France

20. Annecy Hôpital, Annecy, France

21. CHU de Poitiers, Poitiers, France

22. Centre Hospitalier Métropole Savoie Chambéry, Chambéry, France

23. Hospital Universitario de Salamanca, IBSAL, CIBERONC, Salamanca, Spain

24. Hospital Clínic de Barcelona, Barcelona, Spain

25. CHU de Québec, Québec, Canada

26. Tokai University School of Medicine, Kanagawa, Japan

27. Instituto Português de Oncologia de Lisboa, Lisboa, Portugal

28. CHU UCL Namur, Yvoir, Belgium

29. ZNA Stuivenberg, Antwerp, Belgium

30. BC Cancer Centre for Lymphoid Cancer, Vancouver, Canada

31. National Cancer Center Hospital, Tokyo, Japan

32. CHU Montpellier, Montpellier, France

33. Bristol Myers Squibb, Princeton, NJ

Abstract

Clinical trials frequently include multiple end points that mature at different times. The initial report, typically based on the primary end point, may be published when key planned co-primary or secondary analyses are not yet available. Clinical Trial Updates provide an opportunity to disseminate additional results from studies, published in JCO or elsewhere, for which the primary end point has already been reported. The RELEVANCE trial (ClinicalTrials.gov identifier: NCT01650701 ) showed that lenalidomide plus rituximab (R2) provided similar efficacy to rituximab plus chemotherapy (R-chemo) in patients with advanced-stage, previously untreated follicular lymphoma (FL). We report the second interim analysis of the RELEVANCE trial after 6 years of follow-up. Patients with previously untreated grade 1-3a FL were assigned 1:1 to R2 or R-chemo, followed by rituximab maintenance. Coprimary end points were complete response (confirmed/unconfirmed) at week 120 and progression-free survival (PFS). At median follow-up of 72 months, 6-year PFS was 60% and 59% for R2 and R-chemo, respectively (hazard ratio = 1.03 [95% CI, 0.84 to 1.27]). Six-year overall survival was estimated to be 89% in both groups. Median PFS and overall survival were not reached in either group. Overall response after progression was 61% and 59%, and 5-year estimated survival rate after progression was 69% and 74% in the R2 and R-chemo groups, respectively. The transformation rate per year in the R2 and R-chemo groups was 0.68% and 0.45%, and secondary primary malignancies occurred in 11% and 13% ( P = .34), respectively. No new safety signals were observed. R2 continues to demonstrate comparable, durable efficacy and safety versus R-chemo in previously untreated patients with FL and provides an acceptable chemo-free alternative.

Publisher

American Society of Clinical Oncology (ASCO)

Subject

Cancer Research,Oncology

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