Molecular Oncology (May 2023)

Comparative evaluation of PD‐L1 expression in cytology imprints, circulating tumour cells and tumour tissue in non‐small cell lung cancer patients

  • Mustafa Abdo,
  • Yassine Belloum,
  • David Heigener,
  • Lutz Welker,
  • Sönke vonWeihe,
  • Milena Schmidt,
  • Nadine Heuer‐Olewinski,
  • Iris Watermann,
  • Marlen Szewczyk,
  • Jolanthe Kropidlowski,
  • Thais Pereira‐Veiga,
  • Hatice Elmas,
  • Sven Perner,
  • Stefan Steurer,
  • Harriet Wikman,
  • Klaus Pantel,
  • Martin Reck

DOI
https://doi.org/10.1002/1878-0261.13415
Journal volume & issue
Vol. 17, no. 5
pp. 737 – 746

Abstract

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Alternative sources of tumour information need to be explored in patients with non‐small cell lung cancer (NSCLC). Here, we compared programmed cell death ligand 1 (PD‐L1) expression on cytology imprints and circulating tumour cells (CTCs) with PD‐L1 tumour proportion score (TPS) from immunohistochemistry staining of tumour tissue from patients with NSCLC. We evaluated PD‐L1 expression using a PD‐L1 antibody (28‐8) in representative cytology imprints, and tissue samples from the same tumour. We report good agreement rates on PD‐L1 positivity (TPS ≥ 1%) and high PD‐L1 expression (TPS ≥ 50%). Considering high PD‐L1 expression, cytology imprints showed a PPV of 64% and a NPV of 85%. CTCs were detected in 40% of the patients and 80% of them were PD‐L1+. Seven patients with PD‐L1 expression of < 1% in tissue samples or cytology imprints had PD‐L1+ CTCs. The addition of PD‐L1 expression in CTCs to cytology imprints markedly improved the prediction capacity for PD‐L1 positivity. A combined analysis of cytological imprints and CTCs provides information on the tumoural PD‐L1 status in NSCLC patients, which might be used when no tumor tissue is available.

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