Correlation of PD-L1 expression on tumour cells between diagnostic biopsies and surgical specimens of lung cancer in real life with respect to biopsy techniques and neoadjuvant treatment.


Journal

Journal of cancer research and clinical oncology
ISSN: 1432-1335
Titre abrégé: J Cancer Res Clin Oncol
Pays: Germany
ID NLM: 7902060

Informations de publication

Date de publication:
May 2023
Historique:
received: 09 02 2022
accepted: 19 05 2022
medline: 14 4 2023
pubmed: 17 6 2022
entrez: 16 6 2022
Statut: ppublish

Résumé

Programmed death-ligand 1 (PD-L1) testing is performed mainly on biopsy specimens in patients with advanced lung cancer. It is questionable whether the small amount of tissue analysed in biopsies may represent the true PD-L1 expression of a tumour. In this retrospective study, PD-L1 expression on tumour cells derived from bronchoscopy brush cytology, endobronchial ultrasound guided transbronchial needle aspiration (EBUS-TBNA), endobronchial biopsy, transbronchial biopsy (TBB) and computed tomography (CT)-guided transthoracic biopsy was compared to the PD-L1 expression of the corresponding surgical resection in lung cancer patients with regard to neoadjuvant treatment in-between. A quantitative comparison between the diagnostic biopsy of the primary tumour with corresponding resected surgical specimens in a total of 113 lung cancer patients (60% male, mean age 65 ± 9 years) revealed a statistically significant correlation of PD-L1 expression on tumour cells (r = 0.58, p< 0.001), for patients without neoadjuvant treatment in-between and for patients who underwent neoadjuvant treatment (both p < 0.001). Using a cut-off value of ≥ 50% PD-L1 TPS for comparing the biopsy samples and resected specimens, the concordance rate was 78% with a Cohen's Kappa of 0.45. A statistically significant concordance for PD-L1 expression on tumour cells between biopsies from primary lung tumour and resected specimen was found, but of uncertain clinical accuracy. The use of a cut-off value of ≥ 50% PD-L1 TPS resulted only in a moderate agreement. Therefore, the interpretation of the PD-L1 determined form biopsy specimens status should only be considered with caution for treatment decisionsQuery.

Identifiants

pubmed: 35708777
doi: 10.1007/s00432-022-04080-4
pii: 10.1007/s00432-022-04080-4
pmc: PMC10097774
doi:

Substances chimiques

CD274 protein, human 0
B7-H1 Antigen 0
Biomarkers, Tumor 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

1747-1754

Informations de copyright

© 2022. The Author(s).

Références

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Auteurs

D Gompelmann (D)

Division of Pulmonology, Department of Internal Medicine II, Medical University Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria. daniela.gompelmann@meduniwien.ac.at.

K Sinn (K)

Department of Thoracic Surgery, Medical University Vienna, Vienna, Austria.

J Brugger (J)

Department for Medical Statistics, Informatics and Intelligent Systems, Medical University of Vienna, Vienna, Austria.

D Bernitzky (D)

Division of Pulmonology, Department of Internal Medicine II, Medical University Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.

B Mosleh (B)

Department of Thoracic Surgery, Medical University Vienna, Vienna, Austria.

H Prosch (H)

Department for Biomedical Imaging and Image-Guided Therapy, Medical University Vienna, Vienna, Austria.

S Geleff (S)

Department of Pathology, Medical University Vienna, Vienna, Austria.

A Blessing (A)

Department of Pathology, Medical University Vienna, Vienna, Austria.

A Tiefenbacher (A)

Department of Pathology, Medical University Vienna, Vienna, Austria.

K Hoetzenecker (K)

Department of Thoracic Surgery, Medical University Vienna, Vienna, Austria.

M Idzko (M)

Division of Pulmonology, Department of Internal Medicine II, Medical University Vienna, Währinger Gürtel 18-20, 1090, Vienna, Austria.

M A Hoda (MA)

Department of Thoracic Surgery, Medical University Vienna, Vienna, Austria.

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Classifications MeSH