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J Thorac Oncol. 2014 Jan;9(1):26-32. doi: 10.1097/JTO.0000000000000024.

Transbronchial biopsy needle rinse solution used for comprehensive biomarker testing in patients with lung cancer.

Author information

1
Departments of *General Thoracic Surgery, §Medical Oncology, Chiba University Graduate School of Medicine, Chiba, Japan; and †Division of Laboratory Medicine and Clinical Genetics and ‡Department of Endoscopic Diagnostics and Therapeutics, Chiba University Hospital, Chiba, Japan.

Abstract

INTRODUCTION:

Although genetic information is essential for molecular targeted therapy for personalized medicine, tissue sampling for genetic analysis remains challenging. We investigated the utility of bronchoscopic sampling in non-small-cell lung cancer (NSCLC) patients compared with conventional histological materials for multiple genetic analyses.

METHODS:

Patients with NSCLC proven by onsite cytological evaluation during bronchoscopic survey were eligible for this study. After conventional needle aspiration biopsy by flexible bronchofiberscopy of primary lesions or convex-probe endobronchial ultrasound of lymph nodes, the used needle was rinsed with saline, and the ultra-microsample (uMS) was used for cytological diagnosis and genetic analysis. Gene mutations and fusion genes were examined by high-resolution melting analysis and direct sequencing. The results from the uMS and those from conventional histological samples were compared.

RESULTS:

A total of 134 lesions (48 primary and 86 metastatic) were analyzed. Adenocarcinoma (n = 80), squamous-cell carcinoma (n = 43), and NSCLC (n = 11) samples were pathologically confirmed in histological cores; however, malignancies were detected in only 45 (34%) of the corresponding uMS. In 62 samples, genetic disorders, including epidermal growth factor receptor (n = 21), K-ras (n = 11), and BRAF mutations (n = 1); anaplastic lymphoma kinase (n = 5), receptor tyrosine kinase (n = 1), and RET fusion genes (n = 1); and silent mutations (n = 22), were identified. In total, 1474 molecular tests were performed, and 1464 tests (99.3%) were identical for both histological samples and uMS.

CONCLUSION:

Bronchoscopic uMS (biopsy needle rinsed fluids) are useful for multiple genetic examinations in NSCLC.

PMID:
24346091
DOI:
10.1097/JTO.0000000000000024
[Indexed for MEDLINE]
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