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Rituximab and Bendamustine (BR) Compared with Rituximab, Bendamustine, and Cytarabine (R-BAC) in Previously Untreated Elderly Patients with Mantle Cell Lymphoma.

Authors :
Bega G
Olivieri J
Riva M
Scapinello G
Paolini R
Finotto S
Sartori R
Lucchini E
Guandalini G
Facchinelli D
Tisi MC
Basso M
Ballotta L
Piazza F
Ferrarini I
Visco C
Source :
Cancers [Cancers (Basel)] 2021 Dec 03; Vol. 13 (23). Date of Electronic Publication: 2021 Dec 03.
Publication Year :
2021

Abstract

Background: Rituximab plus bendamustine (BR), and rituximab, bendamustine, and cytarabine (R-BAC) are well-known induction therapies in elderly patients with mantle cell lymphoma (MCL), according to clinical guidelines. However, a direct comparison between the two regimens has never been performed.<br />Methods: In this multicentre retrospective study, we compared the outcome of patients with newly diagnosed MCL, treated with BR or R-BAC. Primary endpoint was 2-year progression-free survival (PFS). Inclusion bias was assessed using a propensity score stratified by gender, age, MCL morphology, and MIPI score.<br />Results: After adjusting by propensity score, we identified 156 patients (53 BR, 103 R-BAC) with median age of 72 (53-90). Median follow-up was 46 months (range 12-133). R-BAC was administered in a 2-day schedule or with attenuated dose in 51% of patients. Patients treated with R-BAC achieved CR in 91% of cases, as compared with 60% for BR ( p < 0.0001). The 2-year PFS was 87 ± 3% and 64 ± 7% for R-BAC and BR, respectively ( p = 0.001). In terms of toxicity, R-BAC was associated with significantly more pronounced grade 3-4 thrombocytopenia than BR (50% vs. 17%).<br />Conclusions: This study indicates that R-BAC, even when administered with judiciously attenuated doses, is associated with significantly prolonged 2-year PFS than BR in elderly patients with previously untreated MCL.

Details

Language :
English
ISSN :
2072-6694
Volume :
13
Issue :
23
Database :
MEDLINE
Journal :
Cancers
Publication Type :
Academic Journal
Accession number :
34885198
Full Text :
https://doi.org/10.3390/cancers13236089