CD5+ diffuse large B-cell lymphoma has heterogeneous clinical features and poor prognosis: a single-center retrospective study in China

J Int Med Res. 2022 Sep;50(9):3000605221110075. doi: 10.1177/03000605221110075.

Abstract

Objective: De novo CD5-positive (CD5+) diffuse large B-cell lymphoma (DLBCL) has different clinical characteristics compared with CD5-negative (CD5-) DLBCL. However, few studies have been reported in Chinese cohorts. We investigated the clinical features and prognosis of patients with CD5+ DLBCL and summarized the related literature.

Methods: Data from 245 patients with newly diagnosed DLBCL were retrospectively assessed.

Results: Thirty-one and 214 patients were diagnosed with CD5+ DLBCL or CD5- DLBCL, respectively. In the CD5+ DLBCL group, there were significantly higher proportions of patients with older age (≥60 years), International Prognostic Index (IPI) ≥3, Eastern Cooperative Oncology Group (ECOG) scores ≥ 2, bone marrow involvement, positive B-cell lymphoma 2 expression, and positive MYC expression. Survival analysis showed that CD5+ DLBCL had a markedly poorer 2-year progression-free survival than CD5- DLBCL (18.2% vs. 56.2%). Univariate analysis indicated that age ≥60 years, ECOG score ≥ 2, IPI ≥ 3, B symptoms, and no rituximab-based treatment were poor predictive factors for overall survival (OS). Multivariate analysis revealed that B symptoms and no rituximab-based treatment, but not positive CD5 expression, were independent factors for OS.

Conclusions: Patients with CD5+ DLBCL had heterogeneous clinical characteristics and poor survival. The development of more targeted and effective therapies is needed.

Keywords: CD5; diffuse large B-cell lymphoma; heterogeneous; predictive factor; prognosis; survival.

MeSH terms

  • CD5 Antigens / analysis
  • CD5 Antigens / metabolism
  • China
  • Humans
  • Lymphoma, Large B-Cell, Diffuse* / diagnosis
  • Lymphoma, Large B-Cell, Diffuse* / drug therapy
  • Middle Aged
  • Prognosis
  • Proto-Oncogene Proteins c-bcl-2
  • Retrospective Studies
  • Rituximab / therapeutic use
  • Treatment Outcome

Substances

  • CD5 Antigens
  • Proto-Oncogene Proteins c-bcl-2
  • Rituximab