Association of CD204+ macrophages with poor outcomes of malignant lymphomas not in remission treated by allogeneic HCT

Eur J Haematol. 2019 Dec;103(6):578-587. doi: 10.1111/ejh.13324. Epub 2019 Oct 8.

Abstract

Objective: CD204+ tumor-associated macrophages are associated with adverse outcomes of various malignancies. We performed a study to elucidate the role of CD204+ macrophages in allogeneic hematopoietic cell transplantation (allogeneic HCT).

Methods: In a total of 81 patients who received allogeneic HCT for non-remission malignant lymphoma, immunohistochemical staining of CD204 using specimens preserved before allogeneic HCT was performed. According to the average number of CD204+ macrophages in a high-power field, patients were categorized into three groups: low (<25th percentile), intermediate (≥25th percentile and <50th percentile), and high (≥50th percentile).

Results: The B-cell lymphoma proportion was higher in the low group, while T-cell lymphoma and adult T-cell leukemia proportions were higher in the high group. The 3-year overall survival (OS) was poorest in the high group; low vs intermediate vs high = 83.3% vs 43.7% vs 20.2% (P < .01). The 3-year cumulative incidences of relapse were significantly higher in the high group than the intermediate and low groups: 67.0% vs 38.1% vs 18.2% (P < .01). In multivariate analyses, the numbers of CD204+ macrophages were independent risk factors of poorer OS and cumulative incidences of relapse.

Conclusions: CD204+ macrophages might be associated with poorer prognosis in allogeneic HCT for malignant lymphomas.

Keywords: CD204; allogeneic stem cell transplantation; malignant lymphoma; tumor-associated macrophage.

Publication types

  • Clinical Trial

MeSH terms

  • Adult
  • Allografts
  • Female
  • Hematopoietic Stem Cell Transplantation*
  • Humans
  • Lymphoma, B-Cell* / metabolism
  • Lymphoma, B-Cell* / mortality
  • Lymphoma, B-Cell* / pathology
  • Lymphoma, B-Cell* / therapy
  • Lymphoma, T-Cell* / metabolism
  • Lymphoma, T-Cell* / mortality
  • Lymphoma, T-Cell* / pathology
  • Lymphoma, T-Cell* / therapy
  • Macrophages / metabolism*
  • Macrophages / pathology
  • Male
  • Middle Aged
  • Retrospective Studies
  • Scavenger Receptors, Class A / metabolism*

Substances

  • MSR1 protein, human
  • Scavenger Receptors, Class A