Your browser doesn't support javascript.
loading
Endobronchial Ultrasound Guided Transbronchial Needle Aspiration and Next Generation Sequencing Yields.
Sheehan, Kristin N; Khoury, Lara M; Niehaus, Angela G; Mariencheck, William I; Gershner, Katherine A; Dotson, Travis L; Bellinger, Christina R.
Affiliation
  • Sheehan KN; Department of Pulmonary/Critical Care, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA. Knsheeha@wakehealth.edu.
  • Khoury LM; Department of Internal Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
  • Niehaus AG; Department of Pathology, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
  • Mariencheck WI; Department of Pulmonary/Critical Care, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
  • Gershner KA; Department of Pulmonary/Critical Care, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
  • Dotson TL; Department of Pulmonary/Critical Care, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
  • Bellinger CR; Department of Pulmonary/Critical Care, Wake Forest University School of Medicine, Winston-Salem, NC, 27157, USA.
Lung ; 202(3): 317-324, 2024 Jun.
Article in En | MEDLINE | ID: mdl-38687384
ABSTRACT

PURPOSE:

The use of endobronchial ultrasound (EBUS) is standard practice for lung cancer diagnosis and staging. Next generation sequencing (NGS) for detection of genetic alterations is recommended in advanced, non-squamous, non-small-cell lung cancer (NSCLC). Existing protocols for NGS testing are minimal and reported yields vary. This study aimed to determine the yield of EBUS samples obtained for NGS using a sampling protocol at our institution and assess predictive factors to form collection protocols.

METHODS:

We reviewed EBUS bronchoscopies from 2016 to 2021 with non-squamous NSCLC diagnoses. For target lesions suspected to be malignant, the sampling protocol was (a) two slides for on-site evaluation, (b) three to five fine needle aspirations rinsed into saline for immunohistochemical staining and in-house molecular markers, and (c) additional three to five rinses for NGS. Sufficiency for NGS processing was determined by the pathology department.

RESULTS:

Two hundred and seventy-eight non-squamous NSCLC samples were obtained by EBUS (205 adenocarcinoma; 73 not otherwise specified). EBUS was performed under general anesthesia in 75.5% of cases. The overall sample adequacy for NGS testing was 57.5%. Higher adequacy rates were observed when protocol was adhered to 66.0% versus 37.2% (p < 0.001). There was no statistically significant difference based on the size of the lesion or location of the sample.

CONCLUSION:

When a protocol of three to five dedicated needle rinses for NGS was followed, we nearly doubled our sample adequacy rate for NSG as compared to standard care. Studies are needed to determine the ideal collection and processing modality to preserve tissue samples for genetic sequencing.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bronchoscopy / Carcinoma, Non-Small-Cell Lung / High-Throughput Nucleotide Sequencing / Endoscopic Ultrasound-Guided Fine Needle Aspiration / Lung Neoplasms Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Lung Year: 2024 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Bronchoscopy / Carcinoma, Non-Small-Cell Lung / High-Throughput Nucleotide Sequencing / Endoscopic Ultrasound-Guided Fine Needle Aspiration / Lung Neoplasms Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Lung Year: 2024 Document type: Article Affiliation country: