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Updated: May 14, 2026

Oncogenic Gene Fusion Detection Using Anchored Multiplex Polymerase Chain Reaction Followed by Next Generation Sequencing
Published on: July 5, 2019
KIF5B-RET fusions in Chinese patients with non-small cell lung cancer
Weijing Cai1, Chunxia Su, Xuefei Li
1Department of Medical Oncology, Shanghai Pulmonary Hospital, Tongji University School of Medicine, Tongji University Medical School Cancer Institute, Shanghai, People's Republic of China.
Background:
It has been established that "ret proto-oncogene" (RET) fusions are oncogenic drivers in non-small cell lung cancer (NSCLC). The prevalence and clinicopathologic characteristics of RET fusions in Chinese patients with NSCLC remain unclear. The objective of the current study was to determine the prevalence and clinicopathologic characteristics of KIF5B-RET fusions (fusions of the RET and kinesin family member 5B [KIF5B] genes) in Chinese patients with NSCLC.
Methods:
The authors screened for KIF5B-RET fusions in 392 patients with NSCLC using multiplex real-time polymerase chain reaction assay and validated all positive samples using direct sequencing. The relations between KIF5B-RET fusions and clinicopathologic characteristics were analyzed.
Results:
In total, 6 patients (1.5%) were identified who harbored KIF5B-RET fusions. Of these, 4 had adenocarcinoma, 1 had a malignant neuroendocrine tumor, and 1 had squamous cell carcinoma. All patients who were positive for a KIF5B-RET fusion were never-smokers. There was no statistically significant difference in age, sex, smoking status, pathologic stage, or histologic type between patients with and without KIF5B-RET fusions. Patients without KIF5B-RET fusions had a better prognosis than those with KIF5B-RET fusions (median survival, 52.6 months vs 21.0 months; P = .06), with a hazard ratio of 2.398 (95% confidence interval, 0.982-5.856; P = .055) on multivariate analysis. Disease stage (hazard ratio, 2.879) and younger age (<65 years; hazard ratio, 1.485) were identified as independent prognostic factors for better survival.
Conclusions:
KIF5B-RET fusions were quite rare, with a prevalence of approximately 1.5% in Chinese patients with NSCLC, and they were a little more common in patients with adenocarcinoma than in those with squamous carcinoma (1.73% vs 0.84%). In addition, KIF5B-RET fusions also existed in patients with low-grade malignant neuroendocrine tumors.
Insights
KIF5B-RET fusions are rare oncogenic drivers in Chinese non-small cell lung cancer (NSCLC) patients, found in 1.5% of cases. These fusions were associated with a poorer prognosis, highlighting their clinical significance.
Area of Science:
- Oncology
- Genetics
- Pulmonology
Background:
- RET proto-oncogene (RET) fusions are established oncogenic drivers in non-small cell lung cancer (NSCLC).
- The prevalence and characteristics of RET fusions in Chinese NSCLC patients are not well understood.
- This study focuses on KIF5B-RET fusions, a specific type of RET fusion.
Purpose of the Study:
- To determine the prevalence of KIF5B-RET fusions in Chinese NSCLC patients.
- To investigate the clinicopathologic characteristics associated with KIF5B-RET fusions.
- To analyze the prognostic impact of KIF5B-RET fusions on patient survival.
Main Methods:
- Screening of 392 NSCLC patients for KIF5B-RET fusions using multiplex real-time polymerase chain reaction.
- Validation of positive samples through direct sequencing.
- Analysis of the relationship between KIF5B-RET fusions and clinicopathologic features.
Main Results:
- KIF5B-RET fusions were identified in 6 patients (1.5% prevalence).
- Fusions were found in adenocarcinoma, malignant neuroendocrine tumors, and squamous cell carcinoma; all positive patients were never-smokers.
- Patients with KIF5B-RET fusions showed a trend towards poorer prognosis (median survival 21.0 months vs 52.6 months).
Conclusions:
- KIF5B-RET fusions are rare in Chinese NSCLC patients, occurring in approximately 1.5% of cases.
- These fusions were more frequent in adenocarcinoma than squamous cell carcinoma and also present in neuroendocrine tumors.
- Disease stage and younger age (<65) were independent prognostic factors for better survival in NSCLC.
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