AI Article Synopsis

  • The study focused on 72 patients with non-small cell lung cancer (NSCLC) who had mutations in the epidermal growth factor receptor (EGFR) and were treated with the tyrosine kinase inhibitor, erlotinib, between 2009 and 2015.
  • Findings revealed that the median overall survival for these patients was 9.3 months, with significant factors affecting survival including age and hemoglobin levels.
  • The majority of the study population were non-smokers and had adenocarcinoma histology, with a high comorbidity rate, particularly hypertension; 90% of the patients ultimately did not survive by the end of the study.

Article Abstract

The identification of the epidermal growth factor mutation (EGFR) is a positive prognostic factor for survival and therapeutic response to tyrosine kinase inhibitors (TKIs) in patients with non-small cell lung cancer (NSCLC). TKIs are considered first line treatment in Patients with stages IIIB and IV NSCLC. We investigated the survival and prognostic factors in NSCLC patients with the mutation of the EGFR in routine clinical practice. We conducted a retrospective cohort observational study of 72 patients with non-small cell lung cancer (NSCLC) with EGFR gene mutations that received treatment with erlotinib from January 2009 to December 2015. Kaplan-Meier curves were presented. The association between independent variables and survival was analyzed using the Long-Rank test in bivariate analysis and for multivariate analysis, Cox proportional hazards method was used to calculate hazard ratios (HRs) and corresponding 95% confidence intervals (CIs). We included data from 72 patients, which were followed for a total of 1144 patient-months. The majority of patients were female (61.11%), non-smokers (62.50%), and with histological type corresponding to adenocarcinoma (76.38%). The most frequent EGFR gene mutation was the deletion of exon 19 (65.27%). The majority of patients presented with comorbidities (77.78%), most commonly hypertension. Almost all patients had stage IV NSCLC. Out of the 72 cases, 65 (90.28%) died. The median survival was 9.3 months (95% CI, 7.01-16.93). When comparing the survival curves when using the Log Rank Test, histological type (P = 0.01), place of mutation (P = 0.06), hemoglobin (P = 0.01) and age (P = 0.01) were significant associated to overall survival (OS). In multivariate analysis, only age (HR, 1.02; 95% CI, 1-1.04, P = 0.009) and hemoglobin (HR, 0.70; 95% CI, 0.55-0.89, P = 0.003) remained significant. In conclusion, the median OS of NSCLC patients with positive EGFR gene mutation treated with TKI was 9.3 months. Bivariate and multivariate analysis showed that younger age and a higher hemoglobin level were the most important factors associated with survival.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6556612PMC

Publication Analysis

Top Keywords

egfr gene
16
non-small cell
12
cell lung
12
lung cancer
12
mutation egfr
12
multivariate analysis
12
patients
10
survival
8
survival prognostic
8
prognostic factors
8

Similar Publications

Public Health.

Alzheimers Dement

December 2024

Laboratory of Epidemiology and Population Sciences, National Institute on Aging, Baltimore, MD, USA.

Background: Blood-based biomarkers, glial fibrillary acidic protein (GFAP) and neurofilament light chain (NfL), show potential for dementia risk stratification. Yet, their predictive performance for incident dementia in heterogeneous older population with multi-morbidities, is not well tested. This study evaluates their predictive ability for incident dementia accounting for differences in factors affecting health.

View Article and Find Full Text PDF

The underlying mechanisms between cancer stem cells (CSC) and epithelial-mesenchymal transition (EMT) in pancreatic cancer (PC) remain unclear. In this study, we identified TGIF2 as a target gene of CSC using sncRNA and machine learning. TGIF2 is closely related to the expression of SOX2, EGFR, and E-cadherin, indicating poor prognosis.

View Article and Find Full Text PDF

As a putative lung specific oncogene, the transducin-like enhancer of split 1 (TLE1) corepressor drives an anti-apoptotic and pro-epithelial-mesenchymal transition (EMT) gene transcriptional programs in human lung adenocarcinoma (LUAD) cells, thereby promoting anoikis resistance and tumor aggressiveness. Through its survival- and EMT-promoting gene regulatory programs, TLE1 may impact drug sensitivity and resistance in lung cancer cells. In the present study, a novel function of TLE1 was uncovered as an inhibitor of the antitumor effects of the epidermal growth factor receptor tyrosine kinase inhibitor (EGFR-TKI) gefitinib in the human LUAD cell line A549, which exhibits moderate sensitivity to EGFR-TKI.

View Article and Find Full Text PDF

Background: Endothelial cells are integral components of the tumor microenvironment and play a multifaceted role in tumor immunotherapy. Targeting endothelial cells and related signaling pathways can improve the effectiveness of immunotherapy by normalizing tumor blood vessels and promoting immune cell infiltration. However, to date, there have been no comprehensive studies analyzing the role of endothelial cells in the diagnosis and treatment of prostate adenocarcinoma (PRAD).

View Article and Find Full Text PDF

Background: Artificial sweeteners (AS) have been widely utilized in the food, beverage, and pharmaceutical industries for decades. While numerous publications have suggested a potential link between AS and diseases, particularly cancer, controversy still surrounds this issue. This study aims to investigate the association between AS consumption and cancer risk.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!