Abstract

The role of autologous stem cell transplantation (ASCT) as a frontline treatment in patients with diffuse large B cell lymphoma (DLBCL) who are in their first remission has not been fully elucidated in the rituximab era. We analyzed 272 DLBCL patients who received 4–6 cycles of R-CHOP (rituximab, cyclophosphamide, doxorubicin, vincristine and prednisone) or R-CHOP followed by ASCT, from January 2005 to June 2013 in our institution. Multivariate analysis showed the none germinal center B cell (non-GCB) subtype (P=0.014, P=0.012) and International Prognostic Index (IPI) (3–5) (P=0.004, P=0.016) were independent unfavorable predictors of overall survival (OS) and progression-free survival (PFS), respectively. To investigate the treatment effect of upfront ASCT, we selected 94 high-intermediate and high-risk DLBCL patients who achieved complete remission after R-CHOP, with 41 in the ASCT and 53 in the non-ASCT groups. Survival analysis revealed patients who received upfront ASCT compared with those who did not had better OS (3-year OS: 74.5% vs. 50.4%, P=0.029) or PFS (3-year PFS: 59.6% vs. 32.1%, P=0.004), suggesting up-front ASCT following R-CHOP could improve the outcome of high-intermediate and high-risk DLBCL patients.

Highlights

  • Diffuse large B-cell lymphoma (DLBCL) is the most common form of aggressive lymphomas, accounting for 30–40% of newly diagnosed nonHodgkin’s lymphoma (NHL) [1], and is characterized by heterogeneous clinical and biological features [2]

  • Prognostic factors were investigated in patients with diffuse large B cell lymphoma (DLBCL) treated at a single center who received 4–6 cycles of R-CHOP; we evaluated the role of upfront autologous stem cell transplantation (ASCT) in higher risk but chemotherapy-sensitive patients

  • Multivariate analysis showed that patients with higher International Prognostic Index (IPI) scores or none germinal center B cell (non-germinal center B cell (GCB)) subtype had both worse overall survival (OS) and progression-free survival (PFS)

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Summary

Introduction

Diffuse large B-cell lymphoma (DLBCL) is the most common form of aggressive lymphomas, accounting for 30–40% of newly diagnosed nonHodgkin’s lymphoma (NHL) [1], and is characterized by heterogeneous clinical and biological features [2]. One phase III randomized study of rituximab/carmustine, etoposide, cytarabine and melphalan (R-BEAM) compared with iodine-131 tositumomab BEAM with ASCT for relapsed DLBCL, and the result showed that the R-BEAM and B-BEAM regimens produced similar 2-year progression-free survival (PFS) and overall survival (OS) rates [10]. Another two single-center studies did not observe the significant difference in survival between patients receiving first-line rituximab-containing regimens [11, 12]. Using the Center for International Blood and Transplantation (CIBMTR) database, Fenske et al [6]

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