Clinical course of patients with non–small cell lung cancer and epidermal growth factor receptor exon 19 and exon 21 mutations treated with gefitinib or erlotinib

GJ Riely, W Pao, DK Pham, AR Li, N Rizvi… - Clinical cancer …, 2006 - AACR
… 85% to 90% of EGFR mutations, are the EGFR exon 19 deletion that eliminates a … mutations
associated with response to erlotinib or gefitinib, we developed an assay for EGFR exon 19 …

The different efficacy of gefitinib or erlotinib according to epidermal growth factor receptor exon 19 and exon 21 mutations in Korean non-small cell lung cancer …

JM Sun, YW Won, ST Kim, JH Kim, YL Choi… - Journal of cancer …, 2011 - Springer
… EGFR TKI between patients with exon 19 deletions and L858R mutations have not been …
gefitinib or erlotinib with EGFR tumor genotype (exon 19 deletion vs. L858R mutation in exon 21

[HTML][HTML] … gefitinib and erlotinib treatment in non–small-cell lung cancer patients harboring an epidermal growth factor receptor mutation in either exon 19 or 21

SH Lim, JY Lee, JM Sun, JS Ahn, K Park… - Journal of Thoracic …, 2014 - Elsevier
… either exon 19 deletion or the L858R mutation in exon 21, and had received either gefitinib
(n = 228) or erlotinib (… , where 121 pairs of gefitinib-treated and erlotinib-treated patients were …

Lung cancer with epidermal growth factor receptor exon 20 mutations is associated with poor gefitinib treatment response

JY Wu, SG Wu, CH Yang, CH Gow, YL Chang… - Clinical Cancer …, 2008 - AACR
… had a coexisting mutation, L858R in exon 21, in addition to exon 20 mutations (Table 2). …
from “never smokers” and are associated with sensitivity of tumors to gefitinib and erlotinib. …

Comparison of the effectiveness of erlotinib, gefitinib, and afatinib for treatment of non-small cell lung cancer in patients with common and rare EGFR gene mutations

P Krawczyk, DM Kowalski, R Ramlau… - Oncology …, 2017 - spandidos-publications.com
… with common (exon 19 deletions and exon 21 p.Leu858Arg) and rare EGFR mutations. A …
) and rare (n=13) EGFR mutations treated with erlotinib (n=98), gefitinib (n=66) and afatinib (…

A phase III randomised controlled trial of erlotinib vs gefitinib in advanced non-small cell lung cancer with EGFR mutations

JJ Yang, Q Zhou, HH Yan, XC Zhang, HJ Chen… - British journal of …, 2017 - nature.com
… , P=0.022) than those with exon 21 mutations treated with erlotinib or gefitinib, similar to
the … patients with EGFR exon 19 deletions than in those with exon 21 L858R mutations (Jackman …

Comparison of gefitinib and erlotinib in advanced NSCLC and the effect of EGFR mutations

JY Wu, SG Wu, CH Yang, YL Chang, YC Chang… - Lung cancer, 2011 - Elsevier
… /or insertion in exon 20, and substitutions for L858 or L861 in the activation loop in exon 21.
As … , can detect major mutations such as L858R and deletions in exon 19, and less common …

Better survival with EGFR exon 19 than exon 21 mutations in gefitinib-treated non-small cell lung cancer patients is due to differential inhibition of downstream signals

J Zhu, W Zhong, G Zhang, R Li, X Zhang, A Guo… - Cancer letters, 2008 - Elsevier
… NSCLC shows a promising response to epidermal growth factor receptor (EGFR) tyrosine
kinase inhibitors (TKIs) such as gefitinib and erlotinib, which target the molecular pathways of …

… effects of afatinib with gefitinib or Erlotinib in patients with advanced-stage lung adenocarcinoma harboring non-classical epidermal growth factor receptor mutations

YC Shen, GC Tseng, CY Tu, WC Chen, WC Liao… - Lung Cancer, 2017 - Elsevier
Mutations occur within EGFR exons 18–21. Nearly 85%–90% of lung adenocarcinoma
patients with EGFR mutations will have in-frame deletions in exon 19 (Del19) or exon 21

… for the first-line treatment of metastatic non-small cell lung cancer with epidermal growth factor receptor exon 19 deletions or exon 21 (L858R) substitution mutations

S Khozin, GM Blumenthal, X Jiang, K He, K Boyd… - The …, 2014 - academic.oup.com
… , suggesting that the presence of these mutations may be a predictor of response to gefitinib
… tumor mutations with an exon 19 deletion or an exon 21 (L858R) substitution mutation. …