Detecting the spectrum of multigene mutations in non-small cell lung cancer by Snapshot assay
Related Experiment Video
Updated: Apr 29, 2026

Author Spotlight: Advancements in Molecular Biomarker Testing for Non-Squamous Non-Small Cell Lung Cancer
Published on: September 8, 2023
Jian Su1, Xu-Chao Zhang, She-Juan An
1Medical Research Center of Guangdong General Hospital; Guangdong Lung Cancer Institute, Guangdong Academy of Medical Sciences, Guangzhou, Guangdong 510080, P. R. China. syylwu@live.cn.
Abstract:
As molecular targets continue to be identified and more targeted inhibitors are developed for personalized treatment of non-small cell lung cancer (NSCLC), multigene mutation determination will be needed for routine oncology practice and for clinical trials. In this study, we evaluated the sensitivity and specificity of multigene mutation testing by using the Snapshot assay in NSCLC. We retrospectively reviewed a cohort of 110 consecutive NSCLC specimens for which epidermal growth factor receptor (EGFR) mutation testing was performed between November 2011 and December 2011 using Sanger sequencing. Using the Snapshot assay, mutation statuses were detected for EGFR, Kirsten rate sarcoma viral oncogene homolog (KRAS), phosphoinositide-3-kinase catalytic alpha polypeptide (PIK3CA), v-Raf murine sarcoma viral oncogene homolog B1 (BRAF), v-ras neuroblastoma viral oncogene homolog (NRAS), dual specificity mitogen activated protein kinase kinase 1 (MEK1), phosphatase and tensin homolog (PTEN), and human epidermal growth factor receptor 2 (HER2) in patient specimens and cell line DNA. Snapshot data were compared to Sanger sequencing data. Of the 110 samples, 51 (46.4%) harbored at least one mutation. The mutation frequency in adenocarcinoma specimens was 55.6%, and the frequencies of EGFR, KRAS, PIK3CA, PTEN, and MEK1 mutations were 35.5%, 9.1%, 3.6%, 0.9%, and 0.9%, respectively. No mutation was found in the HER2, NRAS, or BRAF genes. Three of the 51 mutant samples harbored double mutations: two PIK3CA mutations coexisted with KRAS or EGFR mutations, and another KRAS mutation coexisted with a PTEN mutation. Among the 110 samples, 47 were surgical specimens, 60 were biopsy specimens, and 3 were cytological specimens; the corresponding mutation frequencies were 51.1%, 41.7%, and 66.7%, respectively (P = 0.532). Compared to Sanger sequencing, Snapshot specificity was 98.4% and sensitivity was 100% (positive predictive value, 97.9%; negative predictive value, 100%). The Snapshot assay is a sensitive and easily customized assay for multigene mutation testing in clinical practice.
Insights
The Snapshot assay accurately detects multiple gene mutations in non-small cell lung cancer (NSCLC) specimens. This sensitive multigene testing is valuable for personalized cancer treatment and clinical trials.
Area of Science:
- Oncology
- Molecular Diagnostics
- Genetics
Background:
- Personalized treatment for non-small cell lung cancer (NSCLC) relies on identifying molecular targets.
- Multigene mutation determination is increasingly essential for routine oncology practice and clinical trials.
Purpose of the Study:
- To evaluate the sensitivity and specificity of the Snapshot assay for multigene mutation testing in NSCLC.
- To compare Snapshot assay results with Sanger sequencing for key cancer-related genes.
Main Methods:
- Retrospective review of 110 NSCLC specimens.
- Multigene mutation analysis using the Snapshot assay for EGFR, KRAS, PIK3CA, BRAF, NRAS, MEK1, PTEN, and HER2.
- Comparison of Snapshot assay data with Sanger sequencing results.
Main Results:
- 51 out of 110 (46.4%) NSCLC specimens harbored at least one mutation.
- Mutation frequencies varied by gene, with EGFR (35.5%) and KRAS (9.1%) being most common in adenocarcinomas.
- The Snapshot assay demonstrated high specificity (98.4%) and perfect sensitivity (100%) compared to Sanger sequencing.
Conclusions:
- The Snapshot assay is a highly sensitive and specific method for multigene mutation testing in NSCLC.
- This assay is a practical and customizable tool for routine clinical oncology and research.
- Multigene testing supports personalized treatment strategies and advancements in NSCLC clinical trials.
More Related Videos
05:17Detection of Targetable Alterations in Non-small Cell Lung Cancer using Next-generation Sequencing
Published on: October 10, 2025
13:24Integration of Wet and Dry Bench Processes Optimizes Targeted Next-generation Sequencing of Low-quality and Low-quantity Tumor Biopsies
Published on: April 11, 2016