Outcomes of older patients with diffuse large B-cell lymphoma treated with R-CHOP: 10-year follow-up of the LNH03-6B trial.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
27 12 2022
Historique:
accepted: 12 06 2022
received: 17 03 2022
pubmed: 24 6 2022
medline: 22 12 2022
entrez: 23 6 2022
Statut: ppublish

Résumé

The LNH03-6B trial was a phase 3 randomized trial evaluating the efficacy of first-line rituximab, cyclophosphamide, doxorubicine, vincristine and prednisone (R-CHOP) delivered every 2 weeks (R-CHOP14) or 3 weeks (R-CHOP21) in patients with diffuse large B-cell lymphoma (DLBCL) aged 60 to 80 years with an aaIPI (age-adjusted International Prognostic Index) score ≥1 (registered as NCT00144755). We implemented a prospective long-term follow-up program at the end of this trial. The primary endpoints were progression-free survival (PFS) and overall survival (OS). Relapse patterns, PFS and OS after the first progression (PFS2 and OS2) were secondary endpoints. LNH03-6B was registered with ClinicalTrials.gov #NCT00144755. In the LNH03-6B trial, 304 and 296 patients were assigned to receive 8 cycles of R-CHOP14 or R-CHOP21, respectively. Long-term follow-up data were investigated for 256 of 384 (67%) patients still alive at the primary analysis. With a median follow-up of 10.1 years, 213 patients progressed, and 140 patients died without progression. The 10-year PFS was 40.4% (95% confidence interval, 35.9-44.9). Ten-year OS was based on 302 deaths and estimated at 50% (43-56). Of the 213 patients, 105 (49%) progressed after second-line therapy, and 77 patients died without a second progression (36%). The 1-year PFS2 and 1-year OS2 were estimated at 37.9% (95% confidence interval, 31.4-44.5) and 55.8% (95% confidence interval, 48.8-62.2), respectively. Ten years after randomization, the outcomes of patients treated for DLBCL were similar according to PFS and OS between the RCHOP-14 and R-CHOP21 groups. Progression or relapse led to poor prognosis after second-line chemotherapy in the pre CAR-T-cell era. Novel approaches in first-line and alternative treatments in second-line treatments are warranted in this population.

Identifiants

pubmed: 35737565
pii: 485662
doi: 10.1182/bloodadvances.2022007609
pmc: PMC9772793
doi:

Substances chimiques

Rituximab 4F4X42SYQ6
Antibodies, Monoclonal, Murine-Derived 0
Prednisone VB0R961HZT
Vincristine 5J49Q6B70F
Cyclophosphamide 8N3DW7272P
Doxorubicin 80168379AG

Banques de données

ClinicalTrials.gov
['NCT00144755']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

6169-6179

Informations de copyright

© 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.

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Auteurs

Vincent Camus (V)

Department of Hematology, Centre Henri Becquerel, Rouen, France.
Institut national de la santé et de la recherche médicale U1245, Centre Henri Becquerel, University of Rouen, Rouen, France.

Aurélien Belot (A)

Department of Biostatistics, Lymphoma Academic Research Organisation, Hôpital Lyon-Sud, Pierre-Bénite, France.

Lucie Oberic (L)

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

David Sibon (D)

Department of Hematology, Necker University Hospital, Paris, France.

Hervé Ghesquières (H)

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

Catherine Thieblemont (C)

Department of Hematology, Centre Hospitalier Universitaire (CHU) Saint Louis, Paris, France.

Christophe Fruchart (C)

Department of Hematology, Institut d'Hématologie de Basse-Normandie, Caen, France.

Olivier Casasnovas (O)

Department of Hematology, University Hospital, Dijon, France.

Jean-Marie Michot (JM)

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

Thierry Jo Molina (TJ)

Department of Pathology, CHU Necker, Paris, France.

André Bosly (A)

Department of Hematology, Centre hospitalier universitaire Dinant Godinne Saint-Elisabeth - UCL-Namur, Namur, Godinne, Belgium.

Clémentine Joubert (C)

Department of Biostatistics, Lymphoma Academic Research Organisation, Hôpital Lyon-Sud, Pierre-Bénite, France.

Corinne Haioun (C)

Lymphoid Malignancies Unit, Henri Mondor University Hospital, Creteil, France.

Emmanuelle Nicolas-Virelizier (E)

Department of Hematology, Centre Leon Berard, Lyon, France.

Pierre Feugier (P)

Department of Hematology, CHU de Nancy, Hopitaux de Brabois, Vandoeuvre-Lès-Nancy, France.

Olivier Fitoussi (O)

Department of Hematology, Polyclinique Bordeaux Nord Aquitaine, Bordeaux, France.

Richard Delarue (R)

Department of Hematology, Necker University Hospital, Paris, France.

Hervé Tilly (H)

Department of Hematology, Centre Henri Becquerel, Rouen, France.
Institut national de la santé et de la recherche médicale U1245, Centre Henri Becquerel, University of Rouen, Rouen, France.

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Classifications MeSH