ERCC1 Is a Predictive Biomarker for Non-small Cell Lung Cancer But Is Antibody-dependent

Anticancer Res. 2021 May;41(5):2653-2660. doi: 10.21873/anticanres.15046.

Abstract

Background/aim: To predict the efficacy of platinum-containing chemotherapy, ERCC1 expression levels were investigated. Studies have shown changes in the performance of anti-ERCC1 antibodies; therefore, predicting chemotherapy efficacy by immunohistochemical assessment of ERCC1 is controversial.

Patients and methods: Twenty-eight patients who received platinum-containing chemotherapy and underwent computed tomography evaluation 6-9 weeks after therapy initiation were retrospectively identified. The tumor samples were evaluated in 2012 and 2018 using the latest anti-ERCC1 antibodies available at those times.

Results: In 2012, the ERCC1 H-score was significantly higher in patients with disease progression than in patients without disease progression (p=0.019). Although the same trend was shown in 2018, there were some inconsistent results between the 2012 and 2018 samples.

Conclusion: Patients with tumors showing low ERCC1 expression had a better disease control rate on platinum-containing chemotherapy. However, since the performance of the antibody changed over time, standardized technology to evaluate ERCC1 expression is needed.

Keywords: ERCC1; Non-small cell lung cancer; chemotherapy; platinum drug.

MeSH terms

  • Aged
  • Aged, 80 and over
  • Antibodies, Anti-Idiotypic / genetics*
  • Antibodies, Anti-Idiotypic / isolation & purification
  • Biomarkers, Tumor / genetics*
  • Carcinoma, Non-Small-Cell Lung / drug therapy*
  • Carcinoma, Non-Small-Cell Lung / genetics
  • Carcinoma, Non-Small-Cell Lung / pathology
  • DNA-Binding Proteins / genetics*
  • Endonucleases / genetics*
  • Female
  • Gene Expression Regulation, Neoplastic / drug effects
  • Humans
  • Male
  • Middle Aged
  • Platinum / administration & dosage

Substances

  • Antibodies, Anti-Idiotypic
  • Biomarkers, Tumor
  • DNA-Binding Proteins
  • Platinum
  • ERCC1 protein, human
  • Endonucleases