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

Author:

Abdo Mustafa1ORCID,Belloum Yassine2ORCID,Heigener David3,Welker Lutz4,von Weihe Sönke1,Schmidt Milena1,Heuer‐Olewinski Nadine1,Watermann Iris1,Szewczyk Marlen1,Kropidlowski Jolanthe2,Pereira‐Veiga Thais2,Elmas Hatice4,Perner Sven567,Steurer Stefan4,Wikman Harriet2,Pantel Klaus2,Reck Martin1

Affiliation:

1. LungenClinic Grosshansdorf, Airway Research Center North German Center for Lung Research Grosshansdorf Germany

2. Department of Tumor Biology University Medical Center Hamburg‐Eppendorf Germany

3. Department of Respiratory Medicine Agaplesion Diakonieklinikum Rotenburg Germany

4. Department of Pathology University Medical Center Hamburg‐Eppendorf Germany

5. Institute of Pathology University Hospital Schleswig‐Holstein Lübeck Germany

6. Pathology, Research Center Borstel Leibniz Lung Center Borstel Germany

7. German Center for Lung Research Luebeck and Borstel Germany

Abstract

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.

Funder

H2020 Marie Skłodowska-Curie Actions

Publisher

Wiley

Subject

Cancer Research,Genetics,Molecular Medicine,General Medicine,Oncology

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