Search Results - "Janne, P A"
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CNS response to osimertinib in patients with T790M-positive advanced NSCLC: pooled data from two phase II trials
Published in Annals of oncology (01-03-2018)“…Central nervous system (CNS) metastases are common in patients with non-small-cell lung cancer (NSCLC). Osimertinib has shown systemic efficacy in patients…”
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ESMO expert consensus statements on the management of EGFR mutant non-small-cell lung cancer
Published in Annals of oncology (01-05-2022)“…The European Society for Medical Oncology (ESMO) held a virtual consensus-building process on epidermal growth factor receptor (EGFR)-mutant non-small-cell…”
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3
MET increased gene copy number and primary resistance to gefitinib therapy in non-small-cell lung cancer patients
Published in Annals of oncology (01-02-2009)“…Background: MET amplification has been detected in ∼20% of non-small-cell lung cancer patients (NSCLC) with epidermal growth factor receptor (EGFR) mutations…”
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Ligand-associated ERBB2/3 activation confers acquired resistance to FGFR inhibition in FGFR3-dependent cancer cells
Published in Oncogene (23-04-2015)“…Somatic alterations of fibroblast growth factor receptors (FGFRs) have been described in a wide range of malignancies. A number of anti-FGFR therapies are…”
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Osimertinib plus platinum–pemetrexed in newly diagnosed epidermal growth factor receptor mutation-positive advanced/metastatic non-small-cell lung cancer: safety run-in results from the FLAURA2 study
Published in ESMO open (01-10-2021)“…The phase III FLAURA2 (NCT04035486) study will evaluate efficacy and safety of first-line osimertinib with platinum–pemetrexed chemotherapy versus osimertinib…”
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Combined effect of ALK and MEK inhibitors in EML4–ALK-positive non-small-cell lung cancer cells
Published in British journal of cancer (14-02-2012)“…Background: Although most non-small-cell lung cancer (NSCLC) patients with the echinoderm microtubule-associated protein-like 4 ( EML4 ) – anaplastic lymphoma…”
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Ultra-deep next-generation sequencing of plasma cell-free DNA in patients with advanced lung cancers: results from the Actionable Genome Consortium
Published in Annals of oncology (01-04-2019)“…Noninvasive genotyping using plasma cell-free DNA (cfDNA) has the potential to obviate the need for some invasive biopsies in cancer patients while also…”
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Clinical benefit of continuing ALK inhibition with crizotinib beyond initial disease progression in patients with advanced ALK-positive NSCLC
Published in Annals of oncology (01-02-2014)“…Crizotinib is approved to treat advanced ALK-positive non-small-cell lung cancer (NSCLC), but most patients ultimately develop progressive disease (PD). We…”
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Antibody-drug conjugates in lung and breast cancer: current evidence and future directions-a position statement from the ETOP IBCSG Partners Foundation
Published in Annals of oncology (01-07-2024)“…Following the approval of the first antibody-drug conjugates (ADCs) in the early 2000s, development has increased dramatically, with 14 ADCs now approved and…”
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Molecular markers of metastatic disease in KRAS-mutant lung adenocarcinoma
Published in Annals of oncology (01-07-2023)“…Prior studies characterized the association of molecular alterations with treatment-specific outcomes in KRAS-mutant (KRASMUT) lung adenocarcinoma (LUAD). Less…”
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Amplification of EGFR T790M causes resistance to an irreversible EGFR inhibitor
Published in Oncogene (22-04-2010)“…Epidermal growth factor receptor (EGFR) tyrosine kinase inhibitors, gefitinib and erlotinib are effective therapies against mutant non-small cell lung cancers…”
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Anti-HER3 monoclonal antibody patritumab sensitizes refractory non-small cell lung cancer to the epidermal growth factor receptor inhibitor erlotinib
Published in Oncogene (18-02-2016)“…Human epidermal growth factor receptor (HER) 3 is aberrantly overexpressed and correlates with poor prognosis in non-small cell lung cancer (NSCLC). Patritumab…”
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Primary resistance to cetuximab therapy in EGFR FISH-positive colorectal cancer patients
Published in British journal of cancer (08-07-2008)“…The impact of KRAS mutations on cetuximab sensitivity in epidermal growth factor receptor fluorescence in situ hybridisation-positive ( EGFR FISH+) metastatic…”
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Allelic dilution obscures detection of a biologically significant resistance mutation in EGFR-amplified lung cancer
Published in The Journal of clinical investigation (01-10-2006)“…EGFR is frequently mutated and amplified in lung adenocarcinomas sensitive to EGFR inhibitors gefitinib and erlotinib. A secondary mutation, T790M, has been…”
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Improving the yield of circulating tumour cells facilitates molecular characterisation and recognition of discordant HER2 amplification in breast cancer
Published in British journal of cancer (11-05-2010)“…Background: Circulating tumour cells (CTCs) offer a non-invasive approach to obtain and characterise metastatic tumour cells, but their usefulness has been…”
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EGFR FISH assay predicts for response to cetuximab in chemotherapy refractory colorectal cancer patients
Published in Annals of oncology (01-04-2008)“…Background: Standardized conditions to distinguish subpopulations of colorectal cancer (CRC) patients more and less sensitive to cetuximab therapy remain…”
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Phase I study of the AXL inhibitor DS-1205c in combination with osimertinib in subjects with metastatic or unresectable EGFR-mutant NSCLC
Published in Annals of oncology (01-10-2018)Get full text
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A randomized phase II trial of erlotinib or erlotinib and bevacizumab in patients with advanced EGFR mutant non-small cell lung cancer (NSCLC)
Published in Annals of oncology (01-10-2018)Get full text
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Evolution and future perspectives in the treatment of locally advanced non-small cell lung cancer
Published in Annals of oncology (01-07-2007)Get full text
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Targeting HER2 aberrations as actionable drivers in lung cancers: phase II trial of the pan-HER tyrosine kinase inhibitor dacomitinib in patients with HER2-mutant or amplified tumors
Published in Annals of oncology (01-07-2015)“…HER2 mutations and amplifications have been identified as oncogenic drivers in lung cancers. Dacomitinib, an irreversible inhibitor of HER2, EGFR (HER1), and…”
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