Clinicopathologic correlates of MYD88 L265P mutation and programmed cell death (PD-1) pathway in primary central nervous system lymphoma

Leuk Lymphoma. 2019 Dec;60(12):2880-2889. doi: 10.1080/10428194.2019.1620942. Epub 2019 Jun 11.

Abstract

Primary central nervous system lymphoma (PCNSL) patients have a poorer prognosis than systemic lymphoma. Gain-of-function MYD88 c.794T > C (p. L265P) mutation and programed cell death-1 (PD-1) pathway alterations are potential targetable pathways. Our study objective was to determine the clinicopathologic correlates of MYD88 mutation and PD-1 alterations in PCNSL and the impact of Epstein-Barr virus (EBV) infection. We studied 53 cases including 13 EBV-associated (EBVpos) PCNSL, 49% harbored MYD88 mutation, none seen in EBVpos PCNSL. MYD88 protein expression did not correlate with MYD88 mutation. T-cell and macrophage infiltration was common. All PD-L1-positive tumors were EBVpos. Two PD-L1 positive tumors showed 9p24.1/PD-L1 locus alterations by Fluorescence In Situ Hybridization. T cells and macrophages expressed PD-1 and/or PD-L1 in 98% and 83% cases, respectively. MYD88 mutation or protein expression and PD-1 or PD-L1 expression did not predict outcome. We hypothesize that EBVpos PCNSL has a distinct activation mechanism, independent of genetic alterations.

Keywords: Epstein–Barr virus; MYD88; PCNSL; PD-1; checkpoint blockade.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Alleles
  • Amino Acid Substitution
  • Biomarkers, Tumor
  • Central Nervous System Neoplasms / diagnosis
  • Central Nervous System Neoplasms / genetics*
  • Central Nervous System Neoplasms / metabolism*
  • Central Nervous System Neoplasms / therapy
  • Combined Modality Therapy
  • Genetic Association Studies
  • Genetic Predisposition to Disease
  • Humans
  • Immunohistochemistry
  • In Situ Hybridization, Fluorescence
  • Lymphocytes, Tumor-Infiltrating / immunology
  • Lymphocytes, Tumor-Infiltrating / metabolism
  • Lymphocytes, Tumor-Infiltrating / pathology
  • Macrophages / immunology
  • Macrophages / metabolism
  • Mutation*
  • Myeloid Differentiation Factor 88 / genetics*
  • Myeloid Differentiation Factor 88 / metabolism
  • Neoplasm Staging
  • Prognosis
  • Programmed Cell Death 1 Receptor / metabolism*
  • Signal Transduction*
  • Survival Analysis
  • T-Lymphocytes / immunology
  • T-Lymphocytes / metabolism

Substances

  • Biomarkers, Tumor
  • MYD88 protein, human
  • Myeloid Differentiation Factor 88
  • Programmed Cell Death 1 Receptor