Abstract

PurposeThe aim of the study was to delineate the disease characteristics, the initial treatment patterns, and survival in patients with mantle cell lymphoma (MCL) managed in the real world.MethodsData of 518 MCL patients from 5 major Chinese Hematology Centers in the period from 2007 to 2017 were retrospectively analyzed.ResultsThe median age was 58 years. Of the patients, 88.6% had Eastern Cooperative Oncology Group Performance Status (ECOG PS) 0–1 and 80.7% had advanced-stage disease. Ki67 expression was <30% in 39.6% of the patients, and 43.2% of patients were categorized into a low-risk group based on the Mantle Cell Lymphoma International Prognostic Index (MIPI) scoring system. Overall, 73.4% of the patients received rituximab as their first-line therapy. The most commonly used chemotherapy was the CHOP-like (cyclophosphamide, hydroxydaunomycin, oncovin, and prednisone) regimen (45.2%), followed by high-dose cytarabine-containing chemotherapy (31.3%) and bendamustine (3.3%). Of the patients, 13.7% (n = 71) underwent consolidative autologous stem cell transplantation (ASCT), and 19.3% (n = 100) received novel agents containing first-line regimens. With a median follow-up time of 52 months, the 3- and 5-year overall survival (OS) rates were 73.7% and 61.4%, respectively. Age ≤60 years, ECOG PS 0–1, stages I–II, normal lactate dehydrogenase (LDH), absence of bone marrow involvement, Ki67 <30%, and lower-risk IPI/MIPI scores were significantly associated with improved OS (p < 0.05). The inclusion of rituximab improved the 5-year OS, with borderline significance (62.5% vs. 55.2%, p = 0.076). High-dose cytarabine-containing chemotherapy showed significant clinical benefit in 5-year OS (72.1% vs. 55.9%, p = 0.010). Patients with ASCT had better 5-year OS in the younger (≤60 years) age group (87.2% vs. 64.8%, p = 0.002).ConclusionThis large retrospective dataset unequivocally confirmed the survival advantage afforded by cytarabine-containing regimen and ASCT in a first-line setting under real-world management in the rituximab era.

Highlights

  • Mantle cell lymphoma (MCL) is an incurable and heterogeneous disease characterized by chromosomal t(11:14)(q13;32) translocation and cyclin D1 overexpression [1]

  • About 27.6% of the patients presented with International Prognostic Index (IPI) of 3–5, and 37.8% had intermediate- and high-risk Mantle Cell Lymphoma International Prognostic Index (MIPI) scores (Table 1)

  • We investigated the association between the clinical features, initial treatment strategies, and outcomes of MCL patients seeking initial treatment at major academic hematology centers within China

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Summary

Introduction

Mantle cell lymphoma (MCL) is an incurable and heterogeneous disease characterized by chromosomal t(11:14)(q13;32) translocation and cyclin D1 overexpression [1]. It represents about 6%–9% of all newly diagnosed cases of non-Hodgkin’s lymphomas (NHLs) in Western countries [1, 2]. There is a paucity of reported data on the initial treatment patterns and clinical outcomes in Chinese patient populations managed in the rituximab era. The aim of the study was to delineate the disease characteristics, treatment strategies, and survival in real-world Chinese MCL patients

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