Epidermal growth factor receptor mutations: association with favorable local tumor control following Gamma Knife radiosurgery in patients with non-small cell lung cancer and brain metastases.
BM = brain metastasis
EGFR
EGFR = epidermal growth factor receptor
GKRS = Gamma Knife radiosurgery
Gamma Knife
KPS = Karnofsky Performance Scale
NSCLC = non–small cell lung cancer
OS = overall survival
RTOG = Radiation Therapy Oncology Group
SRS = stereotactic radiosurgery
TKI = tyrosine kinase inhibitor
WBRT = whole-brain radiotherapy
brain metastasis
epidermal growth factor receptor
mutation
oncology
stereotactic radiosurgery
survival
tumor control
wild type
Journal
Journal of neurosurgery
ISSN: 1933-0693
Titre abrégé: J Neurosurg
Pays: United States
ID NLM: 0253357
Informations de publication
Date de publication:
21 Jun 2019
21 Jun 2019
Historique:
received:
17
02
2019
accepted:
03
04
2019
pubmed:
22
6
2019
medline:
22
6
2019
entrez:
22
6
2019
Statut:
aheadofprint
Résumé
The presence of epidermal growth factor receptor (EGFR) mutations in non-small cell lung cancer (NSCLC) has been associated with elevated radiosensitivity in vitro. However, results from clinical studies on radiosensitivity in cases of NSCLC with EGFR mutations are inconclusive. This paper presents a retrospective analysis of patients with NSCLC who underwent regular follow-up imaging after radiotherapy for brain metastases (BMs). The authors also investigated the influence of EGFR mutations on the efficacy of Gamma Knife radiosurgery (GKRS). This study included 264 patients (1069 BMs) who underwent GKRS treatment and for whom EGFR mutation status, demographics, performance status, and tumor characteristics were available. Radiological images were obtained at 3 months after GKRS and at 3-month intervals thereafter. Kaplan-Meier plots and Cox regression analysis were used to correlate EGFR mutation status and other clinical features with tumor control and overall survival. The tumor control rates and overall 12-month survival rates were 87.8% and 65.5%, respectively. Tumor control rates in the EGFR mutant group versus the EGFR wild-type group were 90.5% versus 79.4% at 12 months and 75.0% versus 24.5% at 24 months. During the 2-year follow-up period after SRS, the intracranial response rate in the EGFR mutant group was approximately 3-fold higher than that in the wild-type group (p < 0.001). Cox regression multivariate analysis identified EGFR mutation status, extracranial metastasis, primary tumor control, and prescribed margin dose as predictors of tumor control (p = 0.004, p < 0.001, p = 0.004, and p = 0.026, respectively). Treatment with a combination of GKRS and tyrosine kinase inhibitors (TKIs) was the most important predictor of overall survival (p < 0.001). The current study demonstrated that, among patients with NSCLC-BMs, EGFR mutations were independent prognostic factors of tumor control. It was also determined that a combination of GKRS and TKI had the most pronounced effect on prolonging survival after SRS. In select patient groups, treatment with SRS in conjunction with EGFR-TKIs provided effective tumor control for NSCLC-BMs.
Identifiants
pubmed: 31226692
doi: 10.3171/2019.4.JNS19446
pii: 2019.4.JNS19446
doi:
pii:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM