Abstract

Pembrolizumab is an immune checkpoint inhibitor (ICI), currently recommended as the first-line treatment for patients with advanced non-small-cell lung cancer (NSCLC) showing ≥50% expression of programmed death-ligand 1 (PD-L1). Previously it was reported that platinum-based chemotherapy may change PD-L1 expression in solid cancers. However, no reports addressing alteration of PD-L1 expression after ICI therapy in NSCLC are available so far. The patients were Japanese males 83 and 87 years old, who were diagnosed with NSCLC based on the transbronchial lung biopsies showing sarcomatoid feature with high PD-L1 expression. They received Pembrolizumab, however, passed away with disease progression on day 27 and day 9, respectively. PD-L1, PD1, and CD8 antibodies were applied to pretreatment tumor biopsies and autopsy specimens. Immunoexpression of all the markers was evaluated using Aperio ImageScope. We found that PD-L1 expression decreased significantly from 75.6% to 13.2% and from 100% to 58.8%, in patients 1 and 2, respectively. This alteration was less prominent in the perinecrotic tumor area. A considerable decrease of PD-L1 score was linked with a little effect of Pembrolizumab in our patients. This association might be one of the contributing mechanisms of resistance to ICI and needs further investigation in large-scale studies.

Highlights

  • IntroductionNon-small-cell lung cancer (NSCLC) accounts for approximately 80% of all lung cancer cases [1]

  • Lung cancer is the leading cause of cancer-related death worldwide

  • Immunostaining with anti-programmed death-ligand 1 (PD-L1) revealed high PD-L1 expression; a tumor proportion score (TPS) after the manual evaluation was reported as 65%

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Summary

Introduction

Non-small-cell lung cancer (NSCLC) accounts for approximately 80% of all lung cancer cases [1]. Introduction of immune checkpoint inhibitor (ICI) therapy significantly improved progression-free and overall survival of patients with NSCLC compared with conventional platinum-based chemotherapy. ICIs, such as Pembrolizumab, are currently recommended as frontline treatment in patients with advanced epidermal growth factor receptor (EGFR) mutations/anaplastic lymphoma kinase (ALK) gene fusions, ROS proto-oncogene 1 (ROS1) gene fusions, and B-Raf proto-oncogene (BRAF) gene mutations wild-type NSCLC and programmed death-ligand 1 (PD-L1) tumor proportion score ≥50% [2,3]. Programmed cell death protein 1 (PD-1) is one of the coinhibitory receptors expressed on the surface of antigen-stimulated T cells. PD-L1 and PD-L2 are its ligands on the surface of tumor cells [4]

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