Abstract

Non-small-cell lung carcinoma (NSCLC) is a disease characterized by the upregulation of programmed death ligand 1 (PD-L1) along with alterations in epidermal growth factor receptor (EGFR) and HER2-neu (HER2) amplification in addition to EGFR mutation. In the present study, the expression of PD-L1 and EGFR and HER2-neu in NSCLC was studied and their expression in relation to various clinicopathological parameters was analysed. We studied 49 core biopsy specimens of NSCLC for PD-L1, EGFR and HER2-neu expressions using immunohistochemistry. Scoring was based on the intensity and percentage of tumour cells expressing the immunomarkers. PD-L1, EGFR and HER2-neu expression was seen in 20.4%, 32.7% and 14.2% of NSCLC, respectively. The analysis showed no significant difference in PD-L1 expression in relation to any clinicopathological parameters. Low or negative EGFR expression was significantly associated with positive lymph node status (P=0.04). HER2-neu expression showed a significant difference in relation to tumour histology (adenocarcinoma; P=0.01). Also, there was no difference noted with PD-L1 expression in relation to EGFR and HER2-neu expression. As our study has a small number of cases, the validation of the predictive and prognostic value of these markers in lung cancer patients requires further studies.

Highlights

  • Lung cancer is the most commonly diagnosed cancer accounting for 11.6% of the total cases and being the main cause of cancer death constituting 18.4% of the total cancer deaths [1]

  • Non-small-cell lung carcinoma (NSCLC) is a disease characterized by the upregulation of programmed death ligand 1 (PD-L1) along with alterations in epidermal growth factor receptor (EGFR) and HER2-neu (HER2) amplification in addition to EGFR mutation

  • According to the American Joint Committee on Cancer (AJCC) tumour staging classification, only 2 cases were of cT1, 9 cases were of cT2, 13 cases of cT3 and 25 were cases of cT4 stage

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Summary

Introduction

Lung cancer is the most commonly diagnosed cancer accounting for 11.6% of the total cases and being the main cause of cancer death constituting 18.4% of the total cancer deaths [1]. A distinguishing feature of NSCLC is the molecular mutation subsets in the epidermal growth factor receptor (EGFR), which is a major oncogenic driver in this cancer [5]. Another notable oncogene addiction in NSCLC is the human epidermal growth factor receptor 2 (HER2-neu) [5]. Some studies have suggested that HER2-neu overexpression in NSCLC is a weak prognostic factor [9]

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