Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma.


Journal

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

Informations de publication

Date de publication:
27 09 2022
Historique:
received: 22 02 2022
accepted: 01 04 2022
pubmed: 20 4 2022
medline: 23 9 2022
entrez: 19 4 2022
Statut: ppublish

Résumé

The objective of this study was to explore differences in outcomes between first-line rituximab plus bendamustine (R-B) and R-CHOP/R-DHAP (rituximab, cyclophosphamide, doxorubicin, vincristine, prednisone, dexamethasone, cytarabine, cisplatin) in transplant-eligible patients with mantle cell lymphoma (MCL). A population-based cohort of 97 patients aged 18 to 65 years with stage II-IV MCL, consecutively treated with R-B was retrospectively identified at BC Cancer. Baseline characteristics, response rates, and outcomes were compared with the cohort of 232 patients with MCL randomized to the R-CHOP/R-DHAP arm of the MCL Younger trial. The primary endpoint was the hazard ratio (HR) of the progression-free survival (PFS) comparison between both groups, adjusted for MCL International Prognostic Index (MIPI), Ki67 index, and blastoid/ pleomorphic morphology. Ann Arbor stage, lactate dehydrogenase, MIPI, blastoid morphology, and MCL35 assignments were similar between both groups. The overall response rate (ORR) to R-B was 90% (54% complete response [CR]); 77% of patients proceeded to autologous stem cell transplantation (ASCT) and 78% received maintenance rituximab (MR). The ORR to R-CHOP/R-DHAP was 94% (54% CR); 78% proceeded to ASCT and 2% received MR. There were no differences in PFS in unadjusted (HR, 0.87; 95% confidence interval [CI], 0.53-1.41; P = .56) or adjusted (HR, 0.79; 95% CI, 0.45-1.37; P = .40) comparisons. There were no clear differences in secondary endpoints in unadjusted or adjusted analyses. This retrospective adjusted comparison of 2 independent cohorts of younger patients with MCL suggests that R-B with ASCT and maintenance rituximab is a feasible and effective first-line treatment, with outcomes comparable to R-CHOP/R-DHAP with ASCT.

Identifiants

pubmed: 35439293
pii: 484992
doi: 10.1182/bloodadvances.2022007371
pmc: PMC9631687
doi:

Substances chimiques

Ki-67 Antigen 0
Cytarabine 04079A1RDZ
Rituximab 4F4X42SYQ6
Vincristine 5J49Q6B70F
Dexamethasone 7S5I7G3JQL
Doxorubicin 80168379AG
Cyclophosphamide 8N3DW7272P
Bendamustine Hydrochloride 981Y8SX18M
Lactate Dehydrogenases EC 1.1.-
Cisplatin Q20Q21Q62J
Prednisone VB0R961HZT

Types de publication

Journal Article Randomized Controlled Trial Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

5285-5294

Subventions

Organisme : NCI NIH HHS
ID : UH2 CA217847
Pays : United States
Organisme : NCI NIH HHS
ID : UH3 CA217847
Pays : United States

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

Diego Villa (D)

BC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.

Eva Hoster (E)

Institute for Medical Information Processing, Biometry, and Epidemiology, Ludwig-Maximilians-Universität München, Munich, Germany.

Olivier Hermine (O)

Hôpital Necker, Assistance Publique Hôpitaux de Paris, University of Paris Descartes, Paris, France.

Wolfram Klapper (W)

Department of Pathology, Hematopathology Section, University-Hospital Schleswig-Holstein, University of Kiel, Kiel, Germany.

Michal Szymczyk (M)

Department of Lymphoid Malignancies, Maria Sklodowska-Curie National Research Institute of Oncology, Warsaw, Poland.

André Bosly (A)

Centre Hospitalier Universitaire - Université Catholique de Louvain Mont-Godinne-Dinant, Yvoir, Belgium.

Michael Unterhalt (M)

Medizinische Klinik III, Ludwig-Maximilians-Universität München, Munich, Germany.

Lisa M Rimsza (LM)

Department of Laboratory Medicine and Pathology, Mayo Clinic, Scottsdale, AZ; and.

Colleen A Ramsower (CA)

Department of Laboratory Medicine and Pathology, Mayo Clinic, Scottsdale, AZ; and.

Ciara L Freeman (CL)

H. Lee Moffitt Cancer Centre & Research Institute and Morsani College of Medicine, University of South Florida, Tampa, FL.

David W Scott (DW)

BC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.

Alina S Gerrie (AS)

BC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.

Kerry J Savage (KJ)

BC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.

Laurie H Sehn (LH)

BC Cancer Centre for Lymphoid Cancer and University of British Columbia, Vancouver, BC, Canada.

Martin Dreyling (M)

Medizinische Klinik III, Ludwig-Maximilians-Universität München, Munich, Germany.

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Classifications MeSH