Assessing the role of cytarabine-based regimens in mantle cell lymphoma: A real world study.

Y Yanal Mufeed Alnimer (University of Kentucky, Lexington, KY) E Eiraj Khan (4Allegheny General Hospital, Internal Medicine, Pittsburgh, United States) R Rimal Ilyas (Allegheny General Hospital, Pittsburgh, PA) A Abigail Arrigo (Allegheny General Hospital, Pittsburgh, PA) T Tejaswi Gadela (Allegheny General Hospital, Pittsburgh, PA) C Chelsea Peterson (15Division of Hematology and Cellular Therapy, Allegheny Health Network, Pittsburgh, PA) M Mahmoud Amr (University of Kentucky, Lexington, KY) R Reinhold Munker (1University of Kentucky, Markey Cancer Center, Lexington, United States) G Gregory P. Monohan (University of Kentucky Department of Biostatistics, Lexington, KY) A Ayman Qasrawi (1University of Kentucky, Lexington, United States) Z Zena Chahine (1University of Kentucky, Markey Cancer Center, Lexington, United States) F Fevzi Firat Yalniz (31Division of Hematology and Blood and Marrow Transplantation, University of Kentucky, Lexington, KY) C Chait Iragavarapu (Hematology & Cellular Therapy, University of Kentucky College of Medicine, Markey Cancer Center, Lexington, KY) Y Yazan Samhouri (Banner MD Anderson Cancer Center, Gilbert, AZ)

Abstract

7058 Background: Mantle cell lymphoma (MCL) is an aggressive subtype of non-Hodgkin lymphoma. For decades, cytarabine-based regimens have been the cornerstone of MCL treatment, offering substantial efficacy but often at the cost of significant toxicity. More recently, non-cytarabine-based regimens, such as bendamustine combined with rituximab, have emerged as a promising alternative, demonstrating comparable efficacy with more favorable toxicity profile. This study aims to compare the clinical efficacy of cytarabine-based (Ara-C) versus non-cytarabine-based (non-Ara-C) regimens. Methods: We conducted a retrospective cohort study for patients diagnosed with MCL between 2010 and 2023 at Allegheny Health Network and Markey Cancer Center. Data pertaining to demographics, MIPIc, Lugano stage and treatments at induction were collected. Patients were divided into two groups based on whether they received cytarabine based regimen during induction (Ara-c) or not (non-Ara-c). Primary outcomes were overall survival (OS) measured from the time of diagnosis to the time of last follow up or death, and relapse free survival (RFS), calculated from the time of diagnosis to the time of relapse, persistent or progressive disease at the last day of follow up. Sensitivity analysis, with censoring on the time of autologous bone marrow transplant (ASCT) was done. RFS and OS were compared between the two groups after weighted propensity score matching (PSM). Results: We identified 223 patients diagnosed with MCL. The median age was 67.7 (IQ 60-74.5), Majority of patients were males (71%). The median MIPIc score was 8.1(IQR 7-9.5). 72 patients (31%) were in the Ara-c group while 151 patients (69%) were in the non-Ara-c group. The median follow-up of 5.6 years (0.95CI 4.91-6.32). Median OS was 13 years (0.95 CI 7.24-NR) and median RFS was 4.1 years (0.95 CI 3-4.96) for the entire cohort. Baseline comparison between the two groups is shown in table_1. After PSM, Median RFS for Ara-c group was 4.8 (IQR=1.8-16.2) yrs VS 3.6 (IQR=1.52-7) yrs for non-Ara-c group (P value 0.03). However, after censoring on ASCT, median RFS for Ara-c group was 4.7 (IQR 1.5-16.2) yrs VS 3.3 (IQR 1.5-6.9) yrs (P value 0.16). Median OS for Ara-c group was 16.2 yrs (IQR=4.3-16.2) vs 12.95 yrs (IQR=3.7-17.8) for non-Ara-c group (P value 0.5), which was the same after censoring on ASCT. Conclusions: In our cohort, cytarabine use in induction chemotherapy for MCL was associated with longer RFS and OS but it did not reach statistical significance. Larger scale studies are warranted to confirm these results. Of note, older and less fit patients received less cytarabine. Cytarabine Other P value Age 64 (57-69) 69 (63-77) 0.013 Eastern Cooperative group 0,1 96% 84% 0.05 MIPIc 7.56 (6.89-7.92) 8.28 (6.97-9.66) 0.01 Consolidation with ASCT 42% 13% <0.01

Article Details

Volume / Issue Vol. 43, Issue 16_suppl
Published June 01, 2025
Pages 7058-7058
ISSN 0732-183X
Publisher Lippincott Williams & Wilkins

Journal Info

Journal of Clinical Oncology

Lippincott Williams & Wilkins

ISSN: 0732-183X Health Sciences

Authors (14)

Y

Yanal Mufeed Alnimer

University of Kentucky, Lexington, KY

E

Eiraj Khan

4Allegheny General Hospital, Internal Medicine, Pittsburgh, United States

R

Rimal Ilyas

Allegheny General Hospital, Pittsburgh, PA

A

Abigail Arrigo

Allegheny General Hospital, Pittsburgh, PA

T

Tejaswi Gadela

Allegheny General Hospital, Pittsburgh, PA

C

Chelsea Peterson

15Division of Hematology and Cellular Therapy, Allegheny Health Network, Pittsburgh, PA

M

Mahmoud Amr

University of Kentucky, Lexington, KY

R

Reinhold Munker

1University of Kentucky, Markey Cancer Center, Lexington, United States

G

Gregory P. Monohan

University of Kentucky Department of Biostatistics, Lexington, KY

A

Ayman Qasrawi

1University of Kentucky, Lexington, United States

Z

Zena Chahine

1University of Kentucky, Markey Cancer Center, Lexington, United States

F

Fevzi Firat Yalniz

31Division of Hematology and Blood and Marrow Transplantation, University of Kentucky, Lexington, KY

C

Chait Iragavarapu

Hematology & Cellular Therapy, University of Kentucky College of Medicine, Markey Cancer Center, Lexington, KY

Y

Yazan Samhouri

Banner MD Anderson Cancer Center, Gilbert, AZ