Abstract

The treatment of patients with diffuse large B cell lymphoma (DLBCL) would be greatly facilitated with a rapid method for determining prognosis that can be performed more easily and earlier than cytological or specific pathological examinations. It has been suggested that newly diagnosed patients with DLBCL who have low maximum standard uptake value (SUVmax) on 18F-fluorodeoxyglucose positron emission tomography (FDG-PET) are more likely to be successfully treated and remain in remission compared with patients with high SUVmax, but this concept has been poorly studied. We retrospectively analyzed 50 patients with de novo DLBCL to evaluate the relationship between the SUVmax and disease progression. For patients with low SUVmax (n = 10) and high SUVmax (n = 40) (P = 0.255), respectively, the 3-year overall survival rates were 90 and 72 %, and the progression-free survival (PFS) rates were 90 and 39 % (P = 0.012). By multivariate analysis, the revised International Prognostics Index (R-IPI) and SUVmax at diagnosis were shown to predict longer PFS. The 3-year PFS for patients with low SUVmax classified into the good prognosis group by R-IPI was 100 vs. 62 % for those with high SUVmax (P = 0.161), and patients with low SUVmax classified into the poor prognosis group by R-IPI was 80 vs. 18 % for those with high SUVmax (P = 0.050). We conclude that the SUVmax on FDG-PET for newly diagnosed patients with DLBCL is an important predictor of disease progression, especially for patients with poor prognosis by R-IPI.

Highlights

  • Diffuse large B cell lymphoma (DLBCL) is the most common aggressive form of non-Hodgkin’s lymphoma

  • If the patients relapse after the initial chemotherapy, their lymphoma can be poorly managed because most DLBCL cases become chemotherapy-resistant unless treated with high-dose chemotherapy with autologous stem cell transplantation (ASCT) [5, 6]

  • Treatment strategies other than R-CHOP are either initially more intensive chemotherapy or high-dose chemotherapy followed by up-front ASCT or newly developed drug

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Summary

Introduction

Diffuse large B cell lymphoma (DLBCL) is the most common aggressive form of non-Hodgkin’s lymphoma. Combination chemotherapy with rituximab is initially administered to most newly diagnosed patients with DLBCL [1,2,3,4]. If the patients relapse after the initial chemotherapy, their lymphoma can be poorly managed because most DLBCL cases become chemotherapy-resistant unless treated with high-dose chemotherapy with autologous stem cell transplantation (ASCT) [5, 6]. Instead of combination chemotherapy with rituximab, other treatments including more intensive chemotherapy, up-front ASCT after the first remission, or other newly developed drugs are required to improve survival of the patients who are at high risk of relapse [7, 8].

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