Abstract

We retrospectively evaluated consecutive patients diagnosed with Mantle cell lymphoma (MCL) between 01 January 2000 and 31 December 2009. Eighty eight patients with MCL were included in the analysis of whom 46 (52%) received abbreviated Hyper‐CVAD (a total of two cycles; with addition of Rituximab since 2005) with an intention of proceeding to autologous hematopoietic cell transplantation (auto‐HCT), with a median age of 58 years. Response rate to induction at auto‐HCT time was 89% and complete response was 61%. Forty four patients received an auto‐HCT with a 5‐year progression‐free survival (PFS) and overall survival (OS) were 31.2% and 62.5%, respectively. There were 42 nontransplant eligible patients with a median age of 72 years, and 5‐year PFS and OS were 0.0% and 39.9%, respectively. The median survival and PFS in the auto‐HCT eligible group were 68 and 33 months, compared to 32 and 12 months in nontransplant eligible group, without a plateauing of the survival curves in either group. Treatment‐related mortality in the auto‐HCT eligible group was 10.9% (n = 5); two patients died during R‐Hyper‐CVAD and 3 (6.8%) experienced transplant‐related mortality. An abbreviated R‐Hyper‐CVAD‐based induction strategy followed by consolidative auto‐HCT is feasible and provides moderate potential of long‐term survival. Further research to define risk‐adapted strategies; to optimize disease control, is required.

Highlights

  • Mantle cell lymphoma (MCL) has a variable course

  • Eighty-­eight patients were included in the analysis of whom 46 (52%) received Hyper-­CVAD with an intention of proceeding to auto-H­ CT, with a median age of 58 years

  • MCL response rate, response duration, and in some Lenz and colleagues from the German Low Grade instances survival have improved as a result of currently Lymphoma Study Group (GLSG) reported the superiority utilized chemo-i­mmunotherapy strategies that are variably of R-­CHOP compared to CHOP in a prospective randfollowed by consolidative high dose therapy, maintenance omized study in terms of Overall response rate (ORR), Complete response (CR) and time to treatment therapy or observation

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Summary

Introduction

Mantle cell lymphoma (MCL) has a variable course. A minority of patients may survive untreated for many years, for most, the disease will follow an aggressive course [1]. Patients with MCL are typically older with a male predominance and present with stage IV disease [2]. MCL cells are characterized as CD20+ CD5+ CD23− with t (11,14) (q13; q32) translocation and cyclin D1 overexpression on immunohistochemistry [1, 2]. Overexpression of cyclin D1 disrupts cell cycle regulation by increasing retinoblastoma protein phosphorylation, leading to the loss of its inhibitory effect on the G1/S cellular transition phase. The detection of cyclin D1 by immunohistochemistry permits distinction of this disease from other lymphoproliferative disorders that might a­ ppear morphologically similar [3]

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