1189P - Prognostic impact of VEGFA in resectable non-small-cell lung cancer

Date 29 September 2014
Event ESMO 2014
Session Poster Display session
Topics Non-Small-Cell Lung Cancer, Early Stage
Translational Research
Presenter Silvia Calabuig Fariñas
Citation Annals of Oncology (2014) 25 (suppl_4): iv409-iv416. 10.1093/annonc/mdu347
Authors S. Calabuig Fariñas1, E. Jantus-Lewintre1, M. Usó1, S. Gallach Garcia1, R. Sirera Perez2, A. Blasco3, C. Camps4
  • 1Molecular Oncology Laboratory, FIHGUV, 46014 - Valencia/ES
  • 2., Universidad Politecnica, 46014 - Valencia/ES
  • 3Medical Oncology, Hospital General Universitario de Valencia, 46014 - Valencia/ES
  • 4Medicine, Universitat de València, 46010 - Valencia/ES

Abstract

Aim

Angiogenesis is a main process which happens in tumors and that promotes its growth, invasive capacity and metastasis. Host genetic variability within VEGF pathway may affect angiogenic signaling and alter patient's sensitivity to anti-angiogenic therapies and therefore the prognostic. The goal in the present study is to analyze the prognostic value of several SNPs in angiogenic genes and the relative expression of those genes, using a cohort of patients diagnosed with resectable non-small cell lung cancer.

Methods

This study included 127 resectable (I-IIIA) NSCLC patients. RNA and DNA extractions from tissues were performed using Trizol®. 20 ng of DNA were used for studies of SNPs allelic discrimination using TaqMan probe [VEGFA gene: + 936C > T (rs3025039), -460T > C (rs833061) and -405C > G (rs2010963)]. Analysis of VEGFA expression was performed by RTqPCR using hydrolysis probes (TaqMan, Applied Biosystems); expression levels were normalized using GUSB as endogenous gene. All statistical analyses were considered significant at p< 0.05.

Results

Baseline characteristics of the patients were: 85% males, median age 65 years [26-82] and 85% were former or current smokers. The most common histological subtype was squamous (46.5%), followed by adenocarcinoma (41.7%). In survival analysis, patients with the CC genotype of SNP rs833061 showed a better prognosis in TTP (NR vs. 35.36 months, p = 0.026), PFS (NR vs. 31.50 months, p = 0.020) or OS (NR vs. 53.30 months, p = 0.026) compared with other genotypes (TC + TT). Patients with higher levels of expression of VEGFA have a worse outcome in TTP (NR vs. 23,67 months, p = 0.043) and OS (82.60 vs. 46.63 months, p= 0.071).

Conclusions

In conclusion, our results show that expression levels and polymorphisms in VEGFA have potential value as prognostic biomarkers in early-stage NSCLC. This work was supported in part, by a grant [RD12/0036/0025] from RTICC, and PI12-02838 from ISCIII.

Disclosure

All authors have declared no conflicts of interest.