Identification of Potential Prognostic and Predictive Immunological Biomarkers in Patients with Stage I and Stage III Non-Small Cell Lung Cancer (NSCLC): A Prospective Exploratory Study.
Rianne D W VaesKobe ReyndersJenny SprootenKathleen T NevolaKasper M A RouschopMarc VooijsAbhishek Dinkarnath GargMaarten LambrechtLizza E L HendriksMarijana RucevicDirk De RuysscherPublished in: Cancers (2021)
Radiotherapy (RT) and chemotherapy can induce immune responses, but not much is known regarding treatment-induced immune changes in patients. This exploratory study aimed to identify potential prognostic and predictive immune-related proteins associated with progression-free survival (PFS) in patients with non-small cell lung cancer (NSCLC). In this prospective study, patients with stage I NSCLC treated with stereotactic body radiation therapy ( n = 26) and patients with stage III NSCLC treated with concurrent chemoradiotherapy ( n = 18) were included. Blood samples were collected before (v1), during (v2), and after RT (v3). In patients with stage I NSCLC, CD244 (HR: 10.2, 95% CI: 1.8-57.4) was identified as a negative prognostic biomarker. In patients with stage III NSCLC, CR2 and IFNGR2 were identified as positive prognostic biomarkers (CR2, HR: 0.00, 95% CI: 0.00-0.12; IFNGR2, HR: 0.04, 95% CI: 0.00-0.46). In addition, analysis of the treatment-induced changes of circulating protein levels over time (Δv2/v3-v1) also identified CXCL10 and IL-10 as negative predictive biomarkers (CXCL10, HR: 3.86, 95% CI: 1.0-14.7; IL-10, HR: 16.92 (2.74-104.36)), although serum-induced interferon (IFN) response was a positive prognostic. In conclusion, we identified several circulating immunogenic proteins that are correlated with PFS in patients with stage I and stage III NSCLC before and during treatment.
Keyphrases
- small cell lung cancer
- advanced non small cell lung cancer
- locally advanced
- radiation therapy
- immune response
- high glucose
- brain metastases
- diabetic rats
- free survival
- drug induced
- dendritic cells
- rectal cancer
- squamous cell carcinoma
- ejection fraction
- end stage renal disease
- endothelial cells
- radiation induced
- toll like receptor
- risk assessment
- inflammatory response
- patient reported outcomes
- combination therapy
- bioinformatics analysis