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BIOMARKER:

EGFR wild-type

i
Other names: EGFR, ERBB, ERBB1, Epidermal growth factor receptor
Entrez ID:
19h
Novel benzoxazole-based hybrids as multi-target inhibitors of aromatase, EGFR, and PI3K with potential anti-breast cancer activity. (PubMed, Bioorg Med Chem)
MTT assay showed that 6 and 9b were 4.5 and 2 times more potent than doxorubicin against MCF-7 cells, while 9a and 13b were 10 and 7.5 times more effective against MDA-MB-231 cells, respectively...Compound 13b exhibited comparable EGFRL858R inhibition to lapatinib and outperformed pictilisib against PI3Kα, PI3Kβ, and PI3Kδ. Compound 6 showed greater ARO inhibition than letrozole, while being slightly less potent than pictilisib against PI3Kα and PI3Kβ...Docking studies supported the in vitro enzymatic inhibition assays results. Thus, 9b and 13d are potent anti-breast cancer benzoxazoles with selective ARO and PI3kα inhibition activity, respectively, while 6, 9a, and 13b are multi-target inhibitors exhibiting other anticancer synergistic mechanisms.
Journal
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EGFR (Epidermal growth factor receptor) • PIK3CA (Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha) • PIK3CD (Phosphatidylinositol-4 5-Bisphosphate 3-Kinase Catalytic Subunit Delta) • PIK3CB (Phosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit beta) • CASP9 (Caspase 9) • ANXA5 (Annexin A5) • BECN1 (Beclin 1)
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EGFR L858R • EGFR wild-type
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lapatinib • doxorubicin hydrochloride • letrozole • pictilisib (GDC-0941)
1d
Genomic pathogenic alterations in the SWI/SNF complex compromise the outcomes of immunotherapy in Chinese patients with KRAS-mutant NSCLC by downregulating STING expression. (PubMed, BMC Med)
In KRAS-mut NSCLCs with or without STK11/KEAP1 mutations, the GPAs in the DNA-binding genes ARID1A/ARID2 affected the outcomes of immunotherapy, possibly through the downregulation of STING expression.
Journal • IO biomarker
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KRAS (KRAS proto-oncogene GTPase) • STK11 (Serine/threonine kinase 11) • ARID1A (AT-rich interaction domain 1A) • KEAP1 (Kelch Like ECH Associated Protein 1) • PBRM1 (Polybromo 1) • SMARCA4 (SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily A, member 4) • SMARCB1 (SWI/SNF Related, Matrix Associated, Actin Dependent Regulator Of Chromatin, Subfamily B, Member 1) • ARID1B (AT-Rich Interaction Domain 1B) • STING (stimulator of interferon response cGAMP interactor 1) • ARID2 (AT-Rich Interaction Domain 2)
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KRAS mutation • EGFR wild-type • ARID1A mutation • STK11 mutation • KEAP1 mutation
5d
Genomic profiles of primary and acquired MET mutations in NSCLC and the impact of co-mutations on treatment outcomes (PubMed, Zhonghua Yi Xue Za Zhi)
Primary and acquired MET mutations in NSCLC exhibit distinct genomic characteristics. Patients harboring concurrent EGFR mutations in NSCLC may derive less benefit from MET-TKI and ICI, whereas those harboring TP53 co-mutations tend to experience more favorable outcomes compared with TP53 wild-type NSCLC patients when treated with MET-TKI.
Retrospective data • Journal • IO biomarker
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EGFR (Epidermal growth factor receptor) • KRAS (KRAS proto-oncogene GTPase) • TP53 (Tumor protein P53) • MET (MET proto-oncogene, receptor tyrosine kinase) • CDK4 (Cyclin-dependent kinase 4)
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TP53 mutation • KRAS mutation • EGFR mutation • TP53 wild-type • EGFR wild-type • MET mutation
6d
New 2-benzylideneamino-4,5-diphenylfuran-3‑carbonitrile derivatives and their benzylamino analogues: Synthesis, in vitro cytotoxicity, protein kinase inhibitory activity and in silico insights. (PubMed, Bioorg Chem)
Furthermore, evaluation of 7c in HCC827 (exon 19 deletion) mutation, which is a cell model highly sensitive to tyrosine kinase inhibitors, showed that the tested compound exhibited lower inhibition than erlotinib...Furthermore, 7c caused an increase in the levels of caspase 3 (4.68 folds) and caspase 9 (4.54 folds) in HCT-116 cells. Additionally, in silico studies of 7c showed a plausible binding mode that correlates with its potent inhibitory activity against the two enzymes, whereas ADME prediction revealed a favorable oral absorption.
Preclinical • Journal • IO biomarker
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EGFR (Epidermal growth factor receptor) • BCL2 (B-cell CLL/lymphoma 2) • CASP3 (Caspase 3) • CASP9 (Caspase 9)
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EGFR exon 19 deletion • EGFR wild-type
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erlotinib
9d
Exploratory Analyses of Patient Preferences for Atezolizumab Subcutaneous Versus Intravenous from the IMscin002 Study in Patients with Non-Small Cell Lung Cancer. (PubMed, Oncol Ther)
Most patients preferred atezolizumab SC regardless of baseline characteristics, mean injection duration, and cumulative number of SC injections. The trend for a stronger preference was higher among patients who preferred SC than those who preferred IV. Our findings suggest that the proportion of preference for atezolizumab SC over IV is highest in patients aged > 74 years, and that administrator's experience could be an important factor influencing patient preference.
Journal
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EGFR (Epidermal growth factor receptor) • PD-L1 (Programmed death ligand 1)
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EGFR wild-type • ALK wild-type
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Tecentriq (atezolizumab) • Tecentriq Hybreza (atezolizumab and hyaluronidase-tqjs)
15d
Small cell lung cancer transdifferentiation: not a negligible phenomenon. (PubMed, Curr Opin Oncol)
Several molecular mechanisms that can drive SCLC transdifferentiation have been identified. The treatment of transdifferentiated SCLC remains a significant challenge, although promising new strategies are currently under investigation. This review summarizes the current understanding of SCLC transdifferentiation.
Journal • IO biomarker
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EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase) • RET (Ret Proto-Oncogene)
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EGFR mutation • RET fusion • ALK rearrangement • EGFR wild-type
16d
Trial completion date
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EGFR (Epidermal growth factor receptor) • ALK (Anaplastic lymphoma kinase)
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EGFR wild-type • ALK wild-type
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Imfinzi (durvalumab) • docetaxel • ceralasertib (AZD6738)
18d
Trial completion
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HER-2 (Human epidermal growth factor receptor 2) • KRAS (KRAS proto-oncogene GTPase) • ALK (Anaplastic lymphoma kinase) • PTEN (Phosphatase and tensin homolog) • PI3K (Phosphoinositide 3-kinases)
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ALK rearrangement • EGFR wild-type • KRAS wild-type • RAS wild-type • ALK negative
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docetaxel • Tyvyt (sintilimab) • albumin-bound paclitaxel • afuresertib (LAE002)
23d
Application of pleural effusion cell blocks for immunohistochemistry and EGFR gene mutation testing for advanced lung cancer. (PubMed, Exp Ther Med)
Furthermore, patients with EGFR-mutant lung adenocarcinoma undergoing treatment with EGFR tyrosine kinase inhibitors exhibited a significantly extended survival rate compared with those with wild-type EGFR receiving chemotherapy. In conclusion, the present study demonstrated that immunohistochemistry with pleural effusion cell blocks can aid in clarifying the histological subtype of lung cancer, and enable EGFR mutation detection, which can effectively guide molecular targeted therapy.
Journal • Pleural effusion
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EGFR (Epidermal growth factor receptor)
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EGFR mutation • EGFR L858R • EGFR wild-type • EGFR L861Q • EGFR G719X • EGFR S768I
25d
Targeted degradation of EGFR 19Del by PROTACs suppresses tumor growth in non-small-cell lung cancer. (PubMed, Front Pharmacol)
We designed and synthesized a series of highly potent degraders based on the first-generation EGFR-TKI gefitinib and a cereblon (CRBN) ligand...In the HCC827 cell-derived xenograft model, compound 14 demonstrates substantial anti-tumor activity and effectively reduces EGFRDel19 protein levels in vivo. With its low molecular weight and excellent in vitro and in vivo efficacy, compound 14 could serve as a promising lead for developing degrader-based therapies targeting mutated EGFR.
Journal
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EGFR (Epidermal growth factor receptor) • CRBN (Cereblon) • ANXA5 (Annexin A5)
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EGFR mutation • EGFR L858R • EGFR exon 19 deletion • EGFR wild-type
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gefitinib
30d
Trial primary completion date
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EGFR (Epidermal growth factor receptor) • MET (MET proto-oncogene, receptor tyrosine kinase)
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EGFR mutation • EGFR wild-type • MET overexpression • MET expression
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Emrelis (telisotuzumab vedotin-tllv)
1m
Association of human papillomavirus infection and epidermal growth factor receptor mutations in inverted sinonasal papilloma: a systematic review and meta-analysis. (PubMed, Eur Arch Otorhinolaryngol)
We found that HPV infection and EGFR mutations seem to play opposite roles in ISP malignant transformation. HPV infection is a possible etiology of ISP and is also associated with its malignant transformation. EGFR mutations in ISP demonstrate prognostic significance with EGFR wild-type ISP being associated with earlier progression to SNSCC. Our meta-analysis demonstrates that there is not mutually exclusive between HPV infection and EGFR mutations in ISP. The result suggests that both HPV infection and EGFR mutations should be considered in the management of ISP.
Retrospective data • Review • Journal
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EGFR (Epidermal growth factor receptor)
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EGFR mutation • EGFR wild-type