Results 21 to 30 of about 2,201,777 (199)

Combatting acquired resistance to osimertinib in EGFR-mutant lung cancer [PDF]

open access: yesTherapeutic Advances in Medical Oncology, 2022
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

SOS2 modulates the threshold of EGFR signaling to regulate osimertinib efficacy and resistance in lung adenocarcinoma

open access: yesMolecular Oncology
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]

open access: yesCell Reports Medicine
: 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]

open access: yesNature Communications, 2019
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

Case report: primary resistance to osimertinib in erlotinib-pretreated lung adenocarcinoma with EGFR T790 M mutation

open access: yesBMC Cancer, 2018
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

open access: yesCell Reports
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]

open access: yesTranslational Lung Cancer Research, 2020
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

Clinical Management in NSCLC Patients With EGFR Mutation After Osimertinib Progression With Unknown Resistance Mechanisms

open access: yesThe Clinical Respiratory Journal
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]

open access: yesFrontiers in Pharmacology, 2022
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

Activation of insulin‐like growth factor‐1 receptor confers acquired resistance to osimertinib in non‐small cell lung cancer with EGFR T790M mutation

open access: yesThoracic Cancer, 2020
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

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