Correlation study of PD-L1, CD4, CD8, and PD-1 in primary diffuse large B-cell lymphoma of the central nervous system

Pathol Res Pract. 2022 Nov:239:154008. doi: 10.1016/j.prp.2022.154008. Epub 2022 Aug 23.

Abstract

We investigated the clinicopathological role of the PD-1/PD-L1 pathway in the primary diffuse large B-cell lymphoma of the central nervous system (PCNS-DLBCL). Standardized staining for PD-L1 was performed by machine staining, and internationally accepted interpretation methods were used. The PD-L1 immunostaining ≥ 20 % of all cells in slices was defined as high expression of PD-L1. CD4, CD8, and PD-1 tumor-infiltrating lymphocytes (TILs) were enumerated, and the median was defined as the cutoff value. Values higher than the median was defined as high expression. Thirty-four cases (64.2 %) showed high expression of PD-L1. PD-L1 expression was associated with a good prognosis when 20 % was considered as cutoff value and had the smallest P value. By contrast, a low number of CD8+ or PD-1+ TILs was associated with poor prognosis. Patients with low expression of PD-L1 had poor overall survival (P = 0.001), and those with increased CD8 or PD-1 TILs tended to have improved overall survival (P = 0.004 and 0.024, respectively). Low number of monocytes, increased number of lymphocytes, IPI score ≥ 2, ECOG PS ≥ 2, LDH ≥ 250, and Ki67 ≥ 70 % were independent prognostic factors for OS. In conclusion, PD-L1 expression, CD8 and PD-1 TILs, monocyte status, and ECOG PS might be prognostic markers and therapeutic targets of PCNS-DLBCL.

Keywords: Cutoff value; PCNS-DLBCL; PD-L1; Prognosis; TILs.

MeSH terms

  • B7-H1 Antigen* / metabolism
  • CD8-Positive T-Lymphocytes / metabolism
  • Central Nervous System / metabolism
  • Central Nervous System / pathology
  • Correlation of Data
  • Humans
  • Lymphocytes, Tumor-Infiltrating / pathology
  • Lymphoma, Large B-Cell, Diffuse* / pathology
  • Prognosis
  • Programmed Cell Death 1 Receptor / metabolism
  • Tumor Microenvironment

Substances

  • B7-H1 Antigen
  • Programmed Cell Death 1 Receptor