Evaluation of lung cancer biomarkers profile for the decision of targeted therapy in EBUS-TBNA cytological samples.


Journal

Scottish medical journal
ISSN: 0036-9330
Titre abrégé: Scott Med J
Pays: Scotland
ID NLM: 2983335R

Informations de publication

Date de publication:
Feb 2022
Historique:
pubmed: 12 2 2022
medline: 27 4 2022
entrez: 11 2 2022
Statut: ppublish

Résumé

Guidelines recommend performing biomarker tests for epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), BRAF and ROS proto-oncogene-1(ROS1) genes and protein expression of programmed death ligand-1(PD-L1) in patients with non-small lung cell carcinoma (NSCLC). Studies reported that endobronchial ultrasound-transbronchial needle aspiration (EBUS-TBNA) can provide sufficient material for cancer biomarker analyses, but there are still concerns about the subject. The purpose of the study was to assess the adequacy of EBUS-TBNA for testing lung cancer biomarkers. We retrospectively reviewed patients with NSCLC whose EBUS-TBNA was analysed for EGFR, ALK, ROS-1, BRAF and PD-L1 expression between December 2011 and December 2020. A total of 394 patients were enrolled in the study. EGFR mutation and ALK fusion were the most common studied biomarkers. EBUS-TBNA adequacy rate for biomarker tests was found 99.0% for EGFR, 99.1 for ALK, 97.2% for ROS1, 100% for BRAF and 99.3% for PD-L1 testing. Multivariate analysis revealed the histological type, history of treatment for NSCL, size, or 18-fluorodeoxyglucose uptake of sampled lesion did not show any association with TBNA adequacy for biomarker testing. EBUS-TBNA can provide adequate material for biomarker testing for EGFR, ALK, ROS-1, BRAF and PD-L1 expression.

Sections du résumé

BACKGROUND BACKGROUND
Guidelines recommend performing biomarker tests for epidermal growth factor receptor (EGFR), anaplastic lymphoma kinase (ALK), BRAF and ROS proto-oncogene-1(ROS1) genes and protein expression of programmed death ligand-1(PD-L1) in patients with non-small lung cell carcinoma (NSCLC). Studies reported that endobronchial ultrasound-transbronchial needle aspiration (EBUS-TBNA) can provide sufficient material for cancer biomarker analyses, but there are still concerns about the subject.
AIM OBJECTIVE
The purpose of the study was to assess the adequacy of EBUS-TBNA for testing lung cancer biomarkers.
METHODS METHODS
We retrospectively reviewed patients with NSCLC whose EBUS-TBNA was analysed for EGFR, ALK, ROS-1, BRAF and PD-L1 expression between December 2011 and December 2020.
RESULTS RESULTS
A total of 394 patients were enrolled in the study. EGFR mutation and ALK fusion were the most common studied biomarkers. EBUS-TBNA adequacy rate for biomarker tests was found 99.0% for EGFR, 99.1 for ALK, 97.2% for ROS1, 100% for BRAF and 99.3% for PD-L1 testing. Multivariate analysis revealed the histological type, history of treatment for NSCL, size, or 18-fluorodeoxyglucose uptake of sampled lesion did not show any association with TBNA adequacy for biomarker testing.
CONCLUSION CONCLUSIONS
EBUS-TBNA can provide adequate material for biomarker testing for EGFR, ALK, ROS-1, BRAF and PD-L1 expression.

Identifiants

pubmed: 35147461
doi: 10.1177/00369330221078995
doi:

Substances chimiques

B7-H1 Antigen 0
Biomarkers, Tumor 0
Proto-Oncogene Proteins 0
Reactive Oxygen Species 0
ErbB Receptors EC 2.7.10.1
Protein-Tyrosine Kinases EC 2.7.10.1
Proto-Oncogene Proteins B-raf EC 2.7.11.1

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

18-27

Auteurs

Aslıhan Gürün Kaya (A)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Aydın Çiledağ (A)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Serhat Erol (S)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Miraç Öz (M)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Deniz Doğan Mülazımoğlu (D)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Özlem Işık (Ö)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Hilal Özakıncı (H)

Department of Pathology, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Fatma Çiftçi (F)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Elif Şen (E)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Koray Ceyhan (K)

Department of Pathology, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Akın Kaya (A)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Demet Karnak (D)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Gökhan Çelik (G)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

Savaş İsmail (S)

Department of Chest Diseases, 63990Ankara University Faculty of Medicine, Ankara, Turkey.

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Classifications MeSH