CSF-1R expression in tumor-associated macrophages is associated with worse prognosis in classical Hodgkin lymphoma

Am J Clin Pathol. 2014 Apr;141(4):573-83. doi: 10.1309/AJCPR92TDDFARISU.

Abstract

Objectives: The aim of this study was to determine the prognostic relevance of colony-stimulating 1 receptor (CSF-1R) expression in both Hodgkin/Reed-Sternberg (HRS) cells and the surrounding cells (non-HRS cells) in patients with classical Hodgkin lymphoma (CHL) .

Methods: Diagnostic tissues from 112 patients with CHL treated with doxorubicin, bleomycin, vinblastine, and dacarbazine were evaluated retrospectively by immunohistochemical analysis for CSF-1R and CD68 and CD163 for tissue-associated macrophages.

Results: High numbers (≥30%) of non-HRS cells expressing CSF-1R conferred inferior event-free survival and overall survival in univariate and multivariate analysis. High numbers of non-HRS cells expressing CSF-1R were significantly associated with a high number of tumor-associated macrophages as detected by CD163 expression (P < .001). In particular, coexpression of CSF-1R and CD163 was associated with a worse survival outcome than either CSF-1R or CD163 expression alone or no expression.

Conclusions: Our data demonstrate that a high number of non-HRS cells expressing CSF-1R are correlated with an increased tumor macrophage content and worse survival.

Keywords: CD163; CD68; Colony-stimulating factor 1 receptor; Hodgkin lymphoma; Prognosis.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Aged
  • Antigens, CD / genetics*
  • Antigens, Differentiation, Myelomonocytic / genetics*
  • Female
  • Hodgkin Disease / genetics*
  • Hodgkin Disease / mortality*
  • Hodgkin Disease / pathology
  • Humans
  • Macrophages / metabolism*
  • Male
  • Middle Aged
  • Prognosis
  • Receptor, Macrophage Colony-Stimulating Factor / genetics*
  • Receptors, Cell Surface / genetics*
  • Retrospective Studies
  • Treatment Outcome

Substances

  • Antigens, CD
  • Antigens, Differentiation, Myelomonocytic
  • CD163 antigen
  • CD68 antigen, human
  • Receptors, Cell Surface
  • Receptor, Macrophage Colony-Stimulating Factor