Clinicopathological characteristics of POLE mutation in patients with non-small-cell lung cancer

Lung Cancer. 2018 Apr:118:57-61. doi: 10.1016/j.lungcan.2018.02.004. Epub 2018 Feb 6.

Abstract

Background: Mutations in polymerase ε (POLE), a DNA polymerase involved in DNA replication and repair, have been investigated in endometrial cancers and response to programmed cell death protein 1 (PD-1)/PD-1 ligand (PD-L1) immunotherapy. However, the frequency of POLE gene mutation in patients with non-small cell lung cancer (NSCLC) has not been reported.

Materials and methods: We assessed POLE mutation in 319 patients with NSCLC by next-generation sequencing (NGS) of 416 cancer-associated genes. Expression of PD-L1, DNA mismatch repair proteins (MMR), and the abundance of CD8-positive tumor infiltrating lymphocytes (TILs) were assayed by immunohistochemistry. Progression-free survival (PFS) was evaluated using the Kaplan-Meier method and compared among groups using log-rank tests.

Results: Nine of the 319 patients (2.8%) harbored POLE mutation. All nine had adenocarcinomas. The median tumor mutational burdens (TMBs) were 12.2/Mb and 7.8/Mb in patients with and without POLE mutation, respectively (P = 0.026). PD-L1, MMR (including MSH2, MSH6, MLH1 and PMS2), and CD8-positive TILs were evaluated in all nine patients. No microsatellite instability was detected, but seven patients had high levels of CD8-positive TILs and five demonstrated PD-L1 staining >25%. One patient receiving the PD-L1 antibody atezolizumab demonstrated a partial response, with a PFS of >8 months.

Conclusion: POLE mutation represents an uncommon phenotype in NSCLC. TMB, PD-L1 expression, and CD8-positive TILs were all higher in patients with mutant compared with wild-type POLE. POLE mutation may thus represent a candidate biomarker for response to immunotherapy in patients with NSCLC.

Keywords: DNA polymerase ε; Immunotherapy; Non-small-cell lung cancer; Tumor mutational burden.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Aged
  • Aged, 80 and over
  • B7-H1 Antigen / metabolism
  • Carcinoma, Non-Small-Cell Lung / genetics*
  • Carcinoma, Non-Small-Cell Lung / mortality
  • Carcinoma, Non-Small-Cell Lung / pathology
  • DNA Polymerase II / genetics*
  • Female
  • High-Throughput Nucleotide Sequencing
  • Humans
  • Immunohistochemistry
  • Lung Neoplasms / genetics*
  • Lung Neoplasms / mortality
  • Lung Neoplasms / pathology
  • Lymphocytes, Tumor-Infiltrating / immunology*
  • Male
  • Middle Aged
  • Mutation / genetics*
  • Poly-ADP-Ribose Binding Proteins / genetics*
  • Survival Analysis

Substances

  • B7-H1 Antigen
  • CD274 protein, human
  • Poly-ADP-Ribose Binding Proteins
  • DNA Polymerase II
  • POLE protein, human