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Updated: Feb 11, 2026

Detection of a Circulating MicroRNA Custom Panel in Patients with Metastatic Colorectal Cancer
Published on: March 14, 2019
Circulating microRNAs associated with prolonged overall survival in lung cancer patients treated with nivolumab
Ann Rita Halvorsen1, Vandana Sandhu1, Mette Sprauten2
1a Department of Cancer Genetics , Institute for Cancer Research, Oslo University Hospital, The Norwegian Radium Hospital , Oslo , Norway.
Background:
The introduction of immune check-point inhibition in non-small cell lung cancer (NSCLC) therapy represents improved prospects for the patients. The response rates to check-point inhibitors are approximately 20% in unselected NSCLC patients. Increasing levels of tumor PD-L1 expression are associated with higher response rates. However, patients with low PD-L1 levels may also have durable responses, and improved strategies for patient stratification are needed.
Material And Methods:
In this study, we investigated circulating microRNAs aiming to identify circulating predictive biomarkers associated with increased overall survival after immune check-point treatment. Using next generation sequencing, we performed microRNA profiling in serum from NSCLC patients (n = 20) treated with nivolumab. Serum samples from 31 patients were used for validation using qPCR assays. Serum samples were collected prior to immune therapy initiation.
Results:
Based on multivariate regression analysis, we identified a signature of seven microRNAs (miR-215-5p, miR-411-3p, miR-493-5p, miR-494-3p, miR-495-3p, miR-548j-5p and miR-93-3p) significantly associated with overall survival (OS) > 6 months in discovery cohort (p = .0003). We further validated this in another similar set of samples (n = 31) and the model was significantly associated with overall survival (OS) > 6 months (p = .001) with sensitivity and specificity of 71% and 90%, respectively.
Conclusions:
In this study of circulating microRNAs, we have identified a 7-miR signature associated with survival in nivolumab-treated NSCLC patients. This signature may lead to better treatment options for patients with NSCLC, but a validation in an independent cohort is needed to confirm the predicted potential.
Insights
A novel seven microRNA signature in the blood predicts survival in non-small cell lung cancer (NSCLC) patients treated with nivolumab. This biomarker discovery could improve treatment selection for NSCLC patients receiving immune checkpoint inhibitors.
Area of Science:
- Oncology
- Molecular Biology
- Immunotherapy
Background:
- Immune checkpoint inhibitors (ICIs) have improved outcomes for non-small cell lung cancer (NSCLC) patients.
- Response rates to ICIs are limited, and patient stratification is needed beyond PD-L1 expression.
- Alternative biomarkers are crucial for predicting treatment response in NSCLC.
Purpose of the Study:
- To identify circulating microRNAs as predictive biomarkers for overall survival in NSCLC patients undergoing ICI therapy.
- To discover a microRNA signature associated with improved survival after nivolumab treatment.
Main Methods:
- Serum microRNA profiling using next-generation sequencing in 20 NSCLC patients treated with nivolumab.
- Validation of a microRNA signature using qPCR in an independent cohort of 31 NSCLC patients.
- Serum samples were collected pre-treatment to identify predictive markers.
Main Results:
- A signature of seven microRNAs (miR-215-5p, miR-411-3p, miR-493-5p, miR-494-3p, miR-495-3p, miR-548j-5p, miR-93-3p) was identified.
- This 7-microRNA signature significantly predicted overall survival >6 months in both discovery and validation cohorts.
- The signature achieved 71% sensitivity and 90% specificity for predicting survival.
Conclusions:
- A 7-microRNA signature in circulation is associated with survival in NSCLC patients treated with nivolumab.
- This signature holds potential as a predictive biomarker for NSCLC immunotherapy.
- Further validation in an independent cohort is required to confirm the clinical utility of this microRNA signature.
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