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


Journal

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

Informations de publication

Date de publication:
12 10 2021
Historique:
received: 18 03 2021
accepted: 04 05 2021
pubmed: 31 8 2021
medline: 3 11 2021
entrez: 30 8 2021
Statut: ppublish

Résumé

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.

Identifiants

pubmed: 34461634
pii: S2473-9529(21)00453-5
doi: 10.1182/bloodadvances.2021004778
pmc: PMC8679665
doi:

Substances chimiques

Antibodies, Monoclonal, Murine-Derived 0

Types de publication

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

Langues

eng

Sous-ensembles de citation

IM

Pagination

3862-3872

Informations de copyright

© 2021 by The American Society of Hematology.

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Auteurs

Vincent Camus (V)

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

Cédric Rossi (C)

Department of Hematology, University Hospital, Dijon, France.

Pierre Sesques (P)

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

Justine Lequesne (J)

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

David Tonnelet (D)

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

Corinne Haioun (C)

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

Eric Durot (E)

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

Alexandre Willaume (A)

Department of Hematology, Lille University Hospital-Hopital Claude Hurriez, Lille, France.

Martin Gauthier (M)

Department of Hematology, IUCT Oncopole, Toulouse, France.

Marie-Pierre Moles-Moreau (MP)

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

Chloé Antier (C)

Department of Hematology, University Hospital, Nantes, France.

Julien Lazarovici (J)

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

Hélène Monjanel (H)

Department of Hematology, CH Aurillac, Aurillac, France.
Department of Hematology, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.

Sophie Bernard (S)

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

Magalie Tardy (M)

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

Caroline Besson (C)

Service d'Hémato-oncologie, Centre Hospitalier de Versailles, Le Chesnay, France.

Laure Lebras (L)

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

Sylvain Choquet (S)

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

Katell Le Du (K)

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

Christophe Bonnet (C)

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

Sarah Bailly (S)

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

Ghandi Damaj (G)

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

Kamel Laribi (K)

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

Hervé Maisonneuve (H)

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

Roch Houot (R)

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

Adrien Chauchet (A)

Department of Hematology, CH Besançon, Besançon, France.

Fabrice Jardin (F)

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

Alexandra Traverse-Glehen (A)

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

Pierre Decazes (P)

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

Stéphanie Becker (S)

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

Alina Berriolo-Riedinger (A)

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

Hervé Tilly (H)

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

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