Skip to search form
Skip to main content
Skip to account menu
Semantic Scholar
Semantic Scholar's Logo
Search 225,190,210 papers from all fields of science
Search
Sign In
Create Free Account
AZD9291
Known as:
2-Propenamide, N-(2-((2-(dimethylamino)ethyl)methylamino)-4-methoxy-5-((4-(1-methyl-1H-indol-3-yl)-2-pyrimidinyl)amino)phenyl)-
, AZD-9291
National Institutes of Health
Create Alert
Alert
Related topics
Related topics
3 relations
Broader (3)
Acrylamides
Aniline Compounds
osimertinib
Papers overview
Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Acquired resistance to AZD9291 as an upfront treatment is dependent on ERK signaling in a preclinical model
B. Ku
,
Moon Ki Choi
,
+4 authors
M. Ahn
PLoS ONE
2018
Corpus ID: 4789007
AZD9291 (osimertinib) is approved for standard care in patients with EGFR T790M-positive non-small cell lung cancer (NSCLC) after…
Expand
2018
2018
Loss of EGFR confers acquired resistance to AZD9291 in an EGFR-mutant non-small cell lung cancer cell line with an epithelial–mesenchymal transition phenotype
Jing Xu
,
Xiaoting Zhao
,
+12 authors
Shucai Zhang
Journal of Cancer Research and Clinical Oncology
2018
Corpus ID: 44151514
PurposeAZD9291 is an irreversible, small-molecule inhibitor which has potency against mutant EGFR- and T790M-resistant mutation…
Expand
Review
2018
Review
2018
Osimertinib for the treatment of patients with EGFR mutation-positive non-small cell lung cancer.
M. Alsharedi
,
H. Bukamur
,
A. Elhamdani
Drugs of Today
2018
Corpus ID: 51617345
Epidermal growth factor receptor (EGFR) mutations, mostly seen in exon 19 or exon 21, are present in roughly 50% of patients with…
Expand
Review
2017
Review
2017
Osimertinib for EGFR T790M mutation-positive non-small cell lung cancer
K. Soejima
,
H. Yasuda
,
Toshiyuki Hirano
Expert Review of Clinical Pharmacology
2017
Corpus ID: 6381299
ABSTRACT Introduction: Significant advances have been made since the development of epidermal growth factor receptor tyrosine…
Expand
2016
2016
Follow up analysis by exosomal miRNAs in EGFR mutated non-small cell lung cancer (NSCLC) patients during osimertinib (AZD9291) treatment: A potential prognostic biomarker tool.
M. Giallombardo
,
J. Chacartegui
,
+5 authors
C. Rolfo
2016
Corpus ID: 81344895
e23035Background: NSCLC patients harboring EGFR mutations are able to receive approved tyrosine kinase inhibitors (TKIs) but to…
Expand
2015
2015
The Allelic Context of the C 797 S Mutation Acquired upon Treatment with Third-Generation EGFR Inhibitors Impacts Sensitivity toSubsequent Treatment Strategies
M. Niederst
,
Haichuan Hu
,
+6 authors
J. Engelman
2015
Corpus ID: 39582677
Purpose: A secondary EGFR mutation, T790M, is the most common resistance mechanism in EGFR-mutant adenocarcinomas that have…
Expand
2015
2015
Liquid biopsies reveal the dynamic nature of resistance mechanisms in solid tumors
C. Meador
,
C. Lovly
Nature Network Boston
2015
Corpus ID: 1656130
Two new studies demonstrate that so-called 'liquid biopsies' may reveal important genomic information needed to monitor treatment…
Expand
2015
2015
A randomized, phase III study (FLAURA) of AZD9291, a novel EGFR-TKI, versus gefitinib or erlotinib in treatment-naïve patients with advanced non-small cell lung cancer and an EGFR-TKI-sensitizing…
S. Ramalingam
,
Y. Rukazenkov
,
K. Thomas
,
J. Soria
2015
Corpus ID: 79991167
TPS8102 Background: EGFR-TKI is the recommended treatment for patients with advanced NSCLC who have an EGFR-TKI-sensitizing…
Expand
2015
2015
AZD9291, a mutant-selective EGFR inhibitor, as first-line treatment for EGFR mutation-positive advanced non-small cell lung cancer (NSCLC): Results from a phase 1 expansion cohort.
S. Ramalingam
,
J. Yang
,
+10 authors
P. Jänne
2015
Corpus ID: 57525748
8000 Background: AZD9291 is an orally administered EGFR TK inhibitor with activity against the sensitizing EGFR mutations (EGFRm…
Expand
2014
2014
EGFR mutation detection in ctDNA from NSCLC patient plasma: A cross-platform comparison of technologies to support the clinical development of AZD9291.
K. Thress
,
R. Brant
,
+7 authors
J. Barrett
2014
Corpus ID: 78292482
8092 Background: EGFR tyrosine kinase inhibitors are highly effective in treating EGFR mutant+ NSCLC. Patients invariably relapse…
Expand
By clicking accept or continuing to use the site, you agree to the terms outlined in our
Privacy Policy
(opens in a new tab)
,
Terms of Service
(opens in a new tab)
, and
Dataset License
(opens in a new tab)
ACCEPT & CONTINUE