Results 21 to 30 of about 2,201,777 (199)
Combatting acquired resistance to osimertinib in EGFR-mutant lung cancer [PDF]
The discovery of activating mutations in epidermal growth factor receptor (EGFR) in non-small-cell lung cancer transformed the care and prognosis of patients and heralded the era of ‘personalized medicine’ in thoracic oncology.
Sun Min Lim +4 more
core +6 more sources
Son of sevenless 1 and 2 (SOS1 and SOS2) are RAS guanine nucleotide exchange factors (RasGEFs) that mediate physiologic and pathologic receptor tyrosine kinase (RTK)‐dependent RAS activation.
Patricia L. Theard +6 more
doaj +2 more sources
A bispecific antibody targeting EGFR and AXL delays resistance to osimertinib [PDF]
: Activating EGFR (epidermal growth factor receptor) mutations can be inhibited by specific tyrosine kinase inhibitors (TKIs), which have changed the landscape of lung cancer therapy. However, due to secondary mutations and bypass receptors, such as AXL (
Simoni-Nieves, Arturo +16 more
core +7 more sources
AXL confers intrinsic resistance to osimertinib and advances the emergence of tolerant cells [PDF]
Resistance to the new generation EGFR-TKI, Osimertinib, can emerge in patients with EGFR-mutated lung cancer. Here, the authors show that AXL, which is activated by osimertinib, can promote the emergence of tolerant lung cancer cell thus conferring ...
Hirokazu Taniguchi +23 more
doaj +2 more sources
Background Among non-small cell lung cancer (NSCLC) patients with acquired T790 M mutation resistance to first-generation epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI), 71% are likely to benefit from osimertinib.
Lin-Peng Zheng +5 more
doaj +2 more sources
Lipid-associated macrophages for osimertinib resistance and leptomeningeal metastases in NSCLC
Summary: Leptomeningeal metastases (LMs) remain a devastating complication of non-small cell lung cancer (NSCLC), particularly following osimertinib resistance.
Kai Yin +29 more
core +4 more sources
Finding chinks in the osimertinib resistance armor [PDF]
The use of small molecule inhibitors directed at specific oncogene targets, including epidermal growth factor receptor (EGFR) mutations, has improved outcomes and defined precision medicine for non-small cell lung cancers (NSCLC). However, despite the impressive responses and improvements in survival seen with these agents, they are rarely curative ...
Leal, Jose Luis +2 more
openaire +2 more sources
Background Osimertinib is approved as a standard treatment for non‐small cell lung cancer (NSCLC) patients with epidermal growth factor receptor (EGFR) mutation by FDA.
Xin Liao +6 more
doaj +2 more sources
Osimertinib Rechallenge With Bevacizumab vs. Chemotherapy Plus Bevacizumab in EGFR-Mutant NSCLC Patients With Osimertinib Resistance [PDF]
At present, treatment options for osimertinib resistance are very limited. Dual inhibition of the vascular endothelial growth factor (VEGF) and epidermal growth factor receptor (EGFR) significantly improved the progression-free survival (PFS) of advanced EGFR-mutant non–small cell lung cancer (NSCLC).
Qingli Cui +6 more
openaire +3 more sources
Background Osimertinib (AZD9291) is a third‐generation EGFR‐tyrosine kinase inhibitor (TKI) that selectively inhibits the activating EGFR mutation and T790M mutation, and is currently used globally to treat EGFR‐mutant non‐small cell lung cancer (NSCLC).
Daisuke Hayakawa +19 more
doaj +1 more source

