Diffuse large B-cell lymphoma (DLBCL) is a heterogeneous group of diseases with variable outcomes. Although several prognostic markers have been developed, specific biomarkers for stratifying treatment strategies have not been fully investigated. This study aimed to analyze the clinical impact of the expression of cluster of differentiation (CD) 38, which is associated with cellular proliferation and disease progression, in patients with de-novo DLBCL. Using flow cytometry analysis, 137 cases with DLBCL were investigated for surface expression of CD38. Based on the cut-off value by the survival classification and regression tree analysis, the patients were categorized into a CD38 HIGH group (n = 37) and CD38 LOW group (n = 100).The 4-years progression-free survival (PFS) was 31.6% in the CD38 HIGH group and 60.7% in the CD38 LOW group (p < 0.001). Multivariate analysis showed the CD38 HIGH group to be associated with significantly worse PFS (adjusted hazard ratio [aHR], 2.15, 95% CI: 1.26-3.68, p = 0.005) and poor overall survival (OS) (aHR, 2.54, 95% CI: 1.25-5.19, p = 0.010) than the CD38 LOW group. In conclusion, we demonstrated that high CD38 expression is an independent adverse prognostic factor associated with poor clinical outcomes compared to low CD38 expression. CD38 expression in DLBCL cells might be useful for predicting outcomes and designing risk-adapted therapies for patients with de-novo DLBCL.
K E Y W O R D Sdiffuse large B-cell lymphoma, CD38, progression free survival
| INTRODUCTIONDiffuse large B-cell lymphoma (DLBCL) is the most common subtype of aggressive non-Hodgkin lymphoma. Chemoimmunotherapy with rituximab, cyclophosphamide, doxorubicin, vincristine, and prednisolone (R-CHOP) leads to cure in approximately 50% to 60% of patients. However, one-third of patients develop relapse or refractory disease, and have particularly poor outcomes. DLBCL represents a heterogeneous group of diseases with variable outcomes that are differentially characterized by clinical manifestations, cell of origin (COO), molecular features, and frequently recurring mutations. 1,2 Owing to the heterogeneity, several prognostic models and/or various prognostic markers have been developed or assessed to predict survival. For example, the clinical prognostic stratification model, international prognostic index (IPI), is a powerful tool for predicting the survival of patients with DLBCL. However, these