Site Editor

Gregory J. Riely, MD, PhD

Advertisement
Advertisement

NTRK Fusions in NSCLC: Improving Detection With Novel Methodology

By: Celeste L. Dixon
Posted: Thursday, February 1, 2024

Results of research conducted by investigators in Brazil indicate that their custom RNA-based nCounter methodology for detecting NTRK fusions in patients with non–small cell lung cancer (NSCLC) suggest it is sensitive and easy to execute as well as efficient in avoiding false-positive identifications of these fusions. It has complete concordance with the RNA-based next-generation sequencing approach, wrote the team in Scientific Reports, yet it appears to be more cost-effective. In fact, it may also prove to be of use in samples with poor quality, such as formalin-fixed paraffin-embedded samples, reported Rui Manuel Reis, MD, PhD, of Barretos Cancer Hospital, São Paulo, and colleagues.

Although the detection of NTRK1, 2, and 3 fusions in small biopsies is challenging, the fusions are important therapeutic targets for all patients with NSCLC. “The [fusions’] prevalence in South American admixed populations [requires] better [exploration],” explained the authors.

They used their nCounter assay to evaluate the frequency and concordance of NTRK fusions in a real-world scenario: 147 consecutive patients with NSCLC at Dr. Reis’ hospital between 2020 and 2022. The concordance rate between immunohistochemistry and nCounter was 40%, and it was 33.4% between immunohistochemistry and RNA-based next-generation sequencing.

Immunohistochemistry revealed that 12 of the 147 patients had pan-NTRK positivity. “Due to the absence of biological material, RNA-based next-generation sequencing and/or nCounter could be performed” in just 6 of those 12, said the team.

“We found one case exhibiting an NTRK1 fusion and another an NTRK3 gene fusion by both RNA-based next-generation sequencing and nCounter techniques. Both NTRK fusions were detected in patients diagnosed with lung adenocarcinoma, with no history of tobacco consumption,” reported Dr. Reis and co-investigators. “Moreover, no concomitant EGFR, KRAS, and ALK gene alterations were detected in NTRK-positive patients.” Additionally, their findings indicated that NTRK fusions in Brazilian patients with NSCLC are relatively rare (1.3%).

Disclosure: The study authors reported no conflicts of interest.


By continuing to browse this site you permit us and our partners to place identification cookies on your browser and agree to our use of cookies to identify you for marketing. Read our Privacy Policy to learn more.