Abstract 47P
Background
Next-generation sequencing (NGS) analysis is considered standard for lung cancer diagnosis in clinical practice. Little is known about the feasibility of NGS using tumor tissue sampled with a 1.1 mm-diameter cryoprobe. We aimed to investigate the suitability of specimens obtained by transbronchial cryobiopsy (TBC) using a 1.1 mm-diameter cryoprobe for NGS analysis.
Methods
Patients with lung cancer who underwent TBC using a 1.1 mm-diameter cryoprobe for NGS testing between October 2020 and April 2023 were enrolled. A 4.0 mm- or 3.0 mm-diameter bronchoscope with radial probe endobronchial ultrasound and virtual bronchoscopic navigation was used to detect peripheral lung lesions. All procedures were performed under fluoroscopic guidance. Data was analyzed retrospectively.
Results
A total of 56 patients underwent TBC using a 1.1-mm cryoprobe for NGS testing during the study period. Most patients (98%) were in the advanced stage of lung cancer (recurrent or inoperable disease of stages III or IV). The diagnostic yield of NGS for DNA and RNA sequencing was 95% each (53 of 56). Of the 53 patients with positive NGS results, 29 (55%) harbored actionable mutations. Details of the reported mutations are shown in the table. Moderate bleeding was found in three patients (5%), and none of the study patients developed life-threatening complications, including pneumothorax or lung infection. Table: 47P
Actionable mutation | No. (%) |
EGFR mutation | |
Common (19del or L858R) | 12 (21) |
Exon 20 insertion | 1 (2) |
EGFR + other | 5 (9) |
ALK fusion | 3 (5) |
ROS1 fusion | 1 (2) |
KRAS G12C | 2 (4) |
BRAF | 0 (0) |
NTRK | 0 (0) |
MET | |
Exon 14 skipping | 1 (2) |
Amplification | 3 (5) |
RET fusion | 1 (2) |
ERBB | 1 (2) |
Conclusions
TBC using a 1.1 mm-diameter cryoprobe is a useful and safe tool for NGS analysis, for both DNA and RNA sequencing.
Legal entity responsible for the study
The authors.
Funding
Has not received any funding.
Disclosure
All authors have declared no conflicts of interest.