Bendamustine or high-dose cytarabine-based induction with rituximab in transplant-eligible mantle cell lymphoma.
Adolescent
Adult
Aged
Antineoplastic Combined Chemotherapy Protocols
/ therapeutic use
Bendamustine Hydrochloride
/ therapeutic use
Cisplatin
/ therapeutic use
Cyclophosphamide
/ therapeutic use
Cytarabine
/ therapeutic use
Dexamethasone
/ therapeutic use
Doxorubicin
/ therapeutic use
Hematopoietic Stem Cell Transplantation
Humans
Ki-67 Antigen
Lactate Dehydrogenases
Lymphoma, Mantle-Cell
/ pathology
Middle Aged
Prednisone
/ therapeutic use
Retrospective Studies
Rituximab
/ therapeutic use
Transplantation, Autologous
Vincristine
/ therapeutic use
Young Adult
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
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
5285-5294Subventions
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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