Four versus six cycles of CHOP chemotherapy in combination with six applications of rituximab in patients with aggressive B-cell lymphoma with favourable prognosis (FLYER): a randomised, phase 3, non-inferiority trial.


Journal

Lancet (London, England)
ISSN: 1474-547X
Titre abrégé: Lancet
Pays: England
ID NLM: 2985213R

Informations de publication

Date de publication:
21 12 2019
Historique:
received: 19 06 2019
revised: 26 10 2019
accepted: 20 11 2019
entrez: 24 12 2019
pubmed: 24 12 2019
medline: 30 1 2020
Statut: ppublish

Résumé

Six cycles of R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone) are the standard treatment for aggressive B-cell non-Hodgkin lymphoma. In the FLYER trial, we assessed whether four cycles of CHOP plus six applications of rituximab are non-inferior to six cycles of R-CHOP in a population of patients with B-cell non-Hodgkin lymphoma with favourable prognosis. This two-arm, open-label, international, multicentre, prospective, randomised phase 3 non-inferiority trial was done at 138 clinical sites in Denmark, Israel, Italy, Norway, and Germany. We enrolled patients aged 18-60 years, with stage I-II disease, normal serum lactate dehydrogenase concentration, ECOG performance status 0-1, and without bulky disease (maximal tumour diameter <7·5 cm). Randomisation was computer-based and done centrally in a 1:1 ratio using the Pocock minimisation algorithm after stratification for centres, stage (I vs II), and extralymphatic sites (no vs yes). Patients were assigned to receive either six cycles of R-CHOP or four cycles of R-CHOP plus two doses of rituximab. CHOP comprised cyclophosphamide (750 mg/m Between Dec 2, 2005, and Oct 7, 2016, 592 patients were enrolled, of whom 295 patients were randomly assigned to receive six cycles of R-CHOP and 297 were assigned to receive four cycles of R-CHOP plus two doses of rituximab. Four patients in the four-cycles group withdrew informed consent before the start of treatment, so 588 patients were included in the intention-to-treat analysis. After a median follow-up of 66 months (IQR 42-100), 3-year progression-free survival of patients who had four cycles of R-CHOP plus two doses of rituximab was 96% (95% CI 94-99), which was 3% better (lower limit of the one-sided 95% CI for the difference was 0%) than six cycles of R-CHOP, demonstrating the non-inferiority of the four-cycles regimen. 294 haematological and 1036 non-haematological adverse events were documented in the four-cycles group compared with 426 haematological and 1280 non-haematological adverse events in the six-cycles group. Two patients, both in the six-cycles group, died during study therapy. In young patients with aggressive B-cell non-Hodgkin lymphoma and favourable prognosis, four cycles of R-CHOP is non-inferior to six cycles of R-CHOP, with relevant reduction of toxic effects. Thus, chemotherapy can be reduced without compromising outcomes in this population. Deutsche Krebshilfe.

Sections du résumé

BACKGROUND
Six cycles of R-CHOP (rituximab plus cyclophosphamide, doxorubicin, vincristine, and prednisone) are the standard treatment for aggressive B-cell non-Hodgkin lymphoma. In the FLYER trial, we assessed whether four cycles of CHOP plus six applications of rituximab are non-inferior to six cycles of R-CHOP in a population of patients with B-cell non-Hodgkin lymphoma with favourable prognosis.
METHODS
This two-arm, open-label, international, multicentre, prospective, randomised phase 3 non-inferiority trial was done at 138 clinical sites in Denmark, Israel, Italy, Norway, and Germany. We enrolled patients aged 18-60 years, with stage I-II disease, normal serum lactate dehydrogenase concentration, ECOG performance status 0-1, and without bulky disease (maximal tumour diameter <7·5 cm). Randomisation was computer-based and done centrally in a 1:1 ratio using the Pocock minimisation algorithm after stratification for centres, stage (I vs II), and extralymphatic sites (no vs yes). Patients were assigned to receive either six cycles of R-CHOP or four cycles of R-CHOP plus two doses of rituximab. CHOP comprised cyclophosphamide (750 mg/m
FINDINGS
Between Dec 2, 2005, and Oct 7, 2016, 592 patients were enrolled, of whom 295 patients were randomly assigned to receive six cycles of R-CHOP and 297 were assigned to receive four cycles of R-CHOP plus two doses of rituximab. Four patients in the four-cycles group withdrew informed consent before the start of treatment, so 588 patients were included in the intention-to-treat analysis. After a median follow-up of 66 months (IQR 42-100), 3-year progression-free survival of patients who had four cycles of R-CHOP plus two doses of rituximab was 96% (95% CI 94-99), which was 3% better (lower limit of the one-sided 95% CI for the difference was 0%) than six cycles of R-CHOP, demonstrating the non-inferiority of the four-cycles regimen. 294 haematological and 1036 non-haematological adverse events were documented in the four-cycles group compared with 426 haematological and 1280 non-haematological adverse events in the six-cycles group. Two patients, both in the six-cycles group, died during study therapy.
INTERPRETATION
In young patients with aggressive B-cell non-Hodgkin lymphoma and favourable prognosis, four cycles of R-CHOP is non-inferior to six cycles of R-CHOP, with relevant reduction of toxic effects. Thus, chemotherapy can be reduced without compromising outcomes in this population.
FUNDING
Deutsche Krebshilfe.

Identifiants

pubmed: 31868632
pii: S0140-6736(19)33008-9
doi: 10.1016/S0140-6736(19)33008-9
pii:
doi:

Substances chimiques

Antineoplastic Agents, Immunological 0
R-CHOP protocol 0
Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Prednisone VB0R961HZT

Banques de données

ClinicalTrials.gov
['NCT00278421']

Types de publication

Clinical Trial, Phase III Comparative Study Equivalence Trial Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2271-2281

Commentaires et corrections

Type : CommentIn
Type : CommentIn

Informations de copyright

Copyright © 2019 Elsevier Ltd. All rights reserved.

Auteurs

Viola Poeschel (V)

Department of Internal Medicine 1 (Oncology, Hematology, Clinical Immunology, and Rheumatology), Saarland University Medical School, Homburg/Saar, Germany. Electronic address: viola.poeschel@uks.eu.

Gerhard Held (G)

Department of Internal Medicine 1, Westpfalz-Klinikum, Kaiserslautern, Germany. Electronic address: gheld@westpfalz-klinikum.de.

Marita Ziepert (M)

Institute for Medical Informatics, Statistics and Epidemiology, University Leipzig, Leipzig, Germany.

Mathias Witzens-Harig (M)

Department of Internal Medicine V, University of Heidelberg, Heidelberg, Germany.

Harald Holte (H)

Department of Oncology, Oslo University Hospital, Oslo, Norway.

Lorenz Thurner (L)

Department of Internal Medicine 1 (Oncology, Hematology, Clinical Immunology, and Rheumatology), Saarland University Medical School, Homburg/Saar, Germany.

Peter Borchmann (P)

Department of Hematology and Oncology, University Hospital of Cologne, Cologne, Germany.

Andreas Viardot (A)

Department of Internal Medicine III, University Hospital Ulm, Ulm, Germany.

Martin Soekler (M)

Department of Internal Medicine II, University Hospital Tuebingen, Tuebingen, Germany.

Ulrich Keller (U)

Department of Internal Medicine III, Klinikum Rechts der Isar der TU München, Munich, Germany.

Christian Schmidt (C)

Department of Medicine III, University Hospital, Munich, Germany.

Lorenz Truemper (L)

Department of Hematology and Oncology, Georg August University of Goettingen, Goettingen, Germany.

Rolf Mahlberg (R)

Department of Internal Medicine I, Klinikum Mutterhaus der Borromaerinnen, Trier, Germany.

Reinhard Marks (R)

Department of Hematology and Oncology, University Medical Center, Freiburg, Germany.

Heinz-Gert Hoeffkes (HG)

Klinikum Fulda Tumorklinik, Fulda, Germany.

Bernd Metzner (B)

Department of Hematology and Oncology, Klinikum Oldenburg, Oldenburg, Germany.

Judith Dierlamm (J)

Department of Internal Medicine II, University Hospital Eppendorf, Hamburg, Germany.

Norbert Frickhofen (N)

Department of Internal Medicine III, Dr Horst-Schmidt-Kliniken Wiesbaden, Wiesbaden, Germany.

Mathias Haenel (M)

Department of Internal Medicine III, Küchwald Hospital Chemnitz, Chemnitz, Germany.

Andreas Neubauer (A)

Department of Hematology, Oncology and Immunology, University Hospital Marburg, Marburg, Germany.

Michael Kneba (M)

Department of Internal Medicine II, City Hospital Kiel, Kiel, Germany.

Francesco Merli (F)

Hematology Azienda Unità Sanitarie Locali-Istituto di Ricovero e Cura a Carattere Scientifico di Reggio Emilia, Reggio Emilia, Italy.

Alessandra Tucci (A)

Hematology Azienda Socio Sanitaria Territoriale Spedali Civili Brescia, Brescia, Italy.

Peter de Nully Brown (P)

Department of Hematology, Rigshospitalet, Copenhagen, Denmark.

Massimo Federico (M)

Dipartimento Chirurgico, Medico, Odontoiatrico e di Scienze Morfologiche con Interesse Trapiantologico, Oncologico e di Medicina Rigenerativa, University of Modena and Reggio Emilia, Modena, Italy.

Eva Lengfelder (E)

Department of Internal Medicine III, University Hospital Mannheim, Mannheim, Germany.

Alice di Rocco (A)

Department of Translational and Precision Medicine, Sapienza University of Rome, Rome, Italy.

Ralf Trappe (R)

Department of Internal Medicine II, Evangelisches Diakonie-Krankenhaus, Bremen, Germany.

Andreas Rosenwald (A)

Institute of Pathology, University of Wuerzburg, and Comprehensive Cancer Center Mainfranken, Wuerzburg, Germany.

Christian Berdel (C)

Department of Radiooncology, Saarland University Medical School, Homburg/Saar, Germany.

Martin Maisenhoelder (M)

Department of Oncology, University Hospital of North Norway, Tromsø, Norway.

Ofer Shpilberg (O)

Department of Hematology, Rabin Medical Center, Beilinson Hospital, Petah-Tiqwa, Israel.

Josif Amam (J)

Department of Internal Medicine 1 (Oncology, Hematology, Clinical Immunology, and Rheumatology), Saarland University Medical School, Homburg/Saar, Germany.

Konstantinos Christofyllakis (K)

Department of Internal Medicine 1 (Oncology, Hematology, Clinical Immunology, and Rheumatology), Saarland University Medical School, Homburg/Saar, Germany.

Frank Hartmann (F)

Department of Internal Medicine 1 (Oncology, Hematology, Clinical Immunology, and Rheumatology), Saarland University Medical School, Homburg/Saar, Germany.

Niels Murawski (N)

Department of Internal Medicine 1 (Oncology, Hematology, Clinical Immunology, and Rheumatology), Saarland University Medical School, Homburg/Saar, Germany.

Stephan Stilgenbauer (S)

Department of Internal Medicine 1 (Oncology, Hematology, Clinical Immunology, and Rheumatology), Saarland University Medical School, Homburg/Saar, Germany.

Maike Nickelsen (M)

Department of Hematology, Oncology and Stem Cell Transplantation, Asklepios Klinik St Georg, Hamburg, Germany.

Gerald Wulf (G)

Department of Hematology and Oncology, Georg August University of Goettingen, Goettingen, Germany.

Bertram Glass (B)

Department of Hematology, Oncology and Stem Cell Transplantation, Asklepios Klinik St Georg, Hamburg, Germany.

Norbert Schmitz (N)

Department of Hematology, Oncology and Stem Cell Transplantation, Asklepios Klinik St Georg, Hamburg, Germany.

Bettina Altmann (B)

Institute for Medical Informatics, Statistics and Epidemiology, University Leipzig, Leipzig, Germany.

Markus Loeffler (M)

Institute for Medical Informatics, Statistics and Epidemiology, University Leipzig, Leipzig, Germany.

Michael Pfreundschuh (M)

Department of Internal Medicine 1 (Oncology, Hematology, Clinical Immunology, and Rheumatology), Saarland University Medical School, Homburg/Saar, Germany.

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