Loss of CD20 expression following treatment with rituximab (chimaeric monoclonal anti-CD20): a retrospective cohort analysis

Br J Haematol. 2001 Sep;114(4):881-3. doi: 10.1046/j.1365-2141.2001.03019.x.

Abstract

A retrospective analysis of CD20 expression following rituximab for B-cell non-Hodgkin's lymphoma demonstrated a significant change in immunophenotype in 6/25 (24%) patients with persistent bone marrow (BM) infiltration. In three out of six patients, the B cells were uniformly CD20-/CD79alpha+, consistent with frank loss of CD20 expression. In the remaining three cases, the BM infiltrate was predominantly (> 80%) CD20-/CD79alpha+. Two of the former but none of the latter three cases achieved a clinical response. In three further cases, the post-treatment BM infiltrate was composed entirely of benign or reactive CD3+ T cells. Frank loss of CD20 was not seen in 25 post-treatment lymph node biopsies. Immunophenotyping is therefore an important adjunct in the diagnosis of BM infiltration following rituximab.

MeSH terms

  • Antibodies, Monoclonal / adverse effects*
  • Antibodies, Monoclonal, Murine-Derived
  • Antigens, CD / immunology
  • Antigens, CD20 / immunology*
  • Antineoplastic Agents / adverse effects*
  • B-Lymphocytes / immunology
  • Bone Marrow Cells / immunology
  • CD3 Complex / immunology
  • CD79 Antigens
  • Humans
  • Immunophenotyping
  • Immunotherapy
  • Leukemic Infiltration
  • Lymphoma, B-Cell / immunology*
  • Lymphoma, B-Cell / therapy
  • Receptors, Antigen, B-Cell / immunology
  • Retrospective Studies
  • Rituximab
  • T-Lymphocytes, Cytotoxic / immunology

Substances

  • Antibodies, Monoclonal
  • Antibodies, Monoclonal, Murine-Derived
  • Antigens, CD
  • Antigens, CD20
  • Antineoplastic Agents
  • CD3 Complex
  • CD79 Antigens
  • CD79A protein, human
  • Receptors, Antigen, B-Cell
  • Rituximab