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Updated: Nov 8, 2025

Oncogenic Gene Fusion Detection Using Anchored Multiplex Polymerase Chain Reaction Followed by Next Generation Sequencing
Published on: July 5, 2019
TRK Fusion Cancer: Patient Characteristics and Survival Analysis in the Real-World Setting
Lyudmila Bazhenova1, Andrew Lokker2, Jeremy Snider2
1Moores Cancer Center, University of California San Diego, San Diego, 3855 Health Sciences Drive, La Jolla, CA, 92037, USA. lbazhenova@health.ucsd.edu.
Neurotrophic tyrosine receptor kinase (NTRK) gene fusions drive cancer, but their prognostic impact is unclear. This study found no statistically significant difference in overall survival between patients with NTRK gene fusions and those without, suggesting NTRK fusions are not a negative prognostic factor.
Area of Science:
- Oncology
- Genomics
- Molecular Biology
Background:
- Neurotrophic tyrosine receptor kinase (NTRK) gene fusions are recognized oncogenic drivers across diverse cancer types.
- While NTRK gene fusions predict response to tropomyosin receptor kinase inhibitors, their prognostic significance in a pan-tumor context remains largely undetermined.
Purpose of the Study:
- To investigate the clinical characteristics and prognostic implications of NTRK gene fusions in a real-world cancer patient cohort.
- To evaluate the overall survival in patients with NTRK gene fusions compared to those with wild-type NTRK genes.
Main Methods:
- Retrospective analysis of a de-identified clinico-genomic database from January 2011 to July 2018.
- Patients were categorized into NTRK gene fusion and NTRK wild-type groups, with 1:4 matching based on demographic and clinical factors.
- Overall survival was assessed using Kaplan-Meier and Cox regression analyses.
Main Results:
- Median overall survival was 12.5 months for the NTRK gene fusion cohort (n=27) versus 16.5 months for the NTRK wild-type cohort (n=107).
- The hazard ratio for overall survival was 1.44 (95% CI 0.61-3.37, p=0.648), indicating no statistically significant difference.
- Co-occurrence of NTRK gene fusions with other actionable biomarkers (e.g., ALK, BRAF, EGFR) was less frequent than in the wild-type group.
Conclusions:
- The study did not find a statistically significant difference in overall survival between patients with and without NTRK gene fusions.
- NTRK gene fusions were associated with a lower frequency of co-occurring targetable biomarkers.
- Further research is warranted to fully elucidate the prognostic role of NTRK gene fusions in diverse cancers.
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