https://scholars.lib.ntu.edu.tw/handle/123456789/494963
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Paz-Ares L | en_US |
dc.contributor.author | Tan E.-H | en_US |
dc.contributor.author | O'Byrne K | en_US |
dc.contributor.author | Zhang L | en_US |
dc.contributor.author | Hirsh V | en_US |
dc.contributor.author | Boyer M | en_US |
dc.contributor.author | CHIH-HSIN YANG | en_US |
dc.contributor.author | Mok T | en_US |
dc.contributor.author | Lee K.H | en_US |
dc.contributor.author | Lu S | en_US |
dc.contributor.author | Shi Y | en_US |
dc.contributor.author | Lee D.H | en_US |
dc.contributor.author | Laskin J | en_US |
dc.contributor.author | Kim D.-W | en_US |
dc.contributor.author | Laurie S.A | en_US |
dc.contributor.author | Kölbeck K | en_US |
dc.contributor.author | Fan J | en_US |
dc.contributor.author | Dodd N | en_US |
dc.contributor.author | Märten A | en_US |
dc.contributor.author | Park K. | en_US |
dc.creator | Paz-Ares L;Tan E.-H;O'Byrne K;Zhang L;Hirsh V;Boyer M;Chih-Hsin Yang;Mok T;Lee K.H;Lu S;Shi Y;Lee D.H;Laskin J;Kim D.-W;Laurie S.A;K?lbeck K;Fan J;Dodd N;M?rten A;Park K. | - |
dc.date.accessioned | 2020-05-26T09:26:42Z | - |
dc.date.available | 2020-05-26T09:26:42Z | - |
dc.date.issued | 2017 | - |
dc.identifier.issn | 0923-7534 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85015712569&doi=10.1093%2fannonc%2fmdw611&partnerID=40&md5=2d80cbe7aa1b93d226fa7aa184566d41 | - |
dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/494963 | - |
dc.description.abstract | Background: In LUX-Lung 7, the irreversible ErbB family blocker, afatinib, significantly improved progression-free survival (PFS), time-to-treatment failure (TTF) and objective response rate (ORR) versus gefitinib in patients with epidermal growth factor receptor (EGFR) mutation-positive non-small-cell lung cancer (NSCLC). Here, we present primary analysis of mature overall survival (OS) data. Patients and methods: LUX-Lung 7 assessed afatinib 40 mg/day versus gefitinib 250 mg/day in treatment-na?ve patients with stage IIIb/IV NSCLC and a common EGFR mutation (exon 19 deletion/L858R). Primary OS analysis was planned after ~213 OS events and ? 32-month follow-up. OS was analysed by a Cox proportional hazards model, stratified by EGFR mutation type and baseline brain metastases. Results: Two-hundred and twenty-six OS events had occurred at the data cut-off (8 April 2016). After a median follow-up of 42.6 months, median OS (afatinib versus gefitinib) was 27.9 versus 24.5 months [hazard ratio (HR) = 0.86, 95% confidence interval (CI) 0.66-1.12, P = 0.2580]. Prespecified subgroup analyses showed similar OS trends (afatinib versus gefitinib) in patients with exon 19 deletion (30.7 versus 26.4 months; HR, 0.83, 95% CI 0.58-1.17, P = 0.2841) and L858R (25.0 versus 21.2 months; HR 0.91, 95% CI 0.62-1.36, P = 0.6585) mutations. Most patients (afatinib, 72.6%; gefitinib, 76.8%) had at least one subsequent systemic anti-cancer treatment following discontinuation of afatinib/gefitinib; 20 (13.7%) and 23 (15.2%) patients received a thirdgeneration EGFR tyrosine kinase inhibitor. Updated PFS (independent review), TTF and ORR data were significantly improved with afatinib. Conclusion: In LUX-Lung 7, there was no significant difference in OS with afatinib versus gefitinib. Updated PFS (independent review), TTF and ORR data were significantly improved with afatinib. ? The Author 2016. | - |
dc.publisher | Oxford University Press | - |
dc.relation.ispartof | Annals of Oncology | - |
dc.subject | Afatinib; Gefitinib; NSCLC; Overall survival | - |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | afatinib; epidermal growth factor receptor; erlotinib; gefitinib; olmutinib; osimertinib; poziotinib; afatinib; antineoplastic agent; EGFR protein, human; epidermal growth factor receptor; gefitinib; quinazoline derivative; acne; adult; Article; brain metastasis; cancer staging; diarrhea; drug substitution; drug treatment failure; drug withdrawal; EGFR gene; exon; fatigue; follow up; gene deletion; gene mutation; human; hypertransaminasemia; interstitial lung disease; kidney failure; liver failure; major clinical study; multicenter study (topic); non small cell lung cancer; overall survival; phase 2 clinical trial (topic); priority journal; proportional hazards model; randomized controlled trial (topic); rash; treatment response; aged; clinical trial; comparative study; controlled study; female; genetics; Kaplan Meier method; lung tumor; male; middle aged; mortality; mutation; non small cell lung cancer; phase 2 clinical trial; randomized controlled trial; treatment outcome; Aged; Antineoplastic Agents; Carcinoma, Non-Small-Cell Lung; Female; Humans; Kaplan-Meier Estimate; Lung Neoplasms; Male; Middle Aged; Mutation; Proportional Hazards Models; Quinazolines; Receptor, Epidermal Growth Factor; Treatment Outcome | - |
dc.title | Afatinib versus gefitinib in patients with EGFR mutation-positive advanced non-small-cell lung cancer: Overall survival data from the phase IIb LUX-Lung 7 trial | en_US |
dc.type | journal article | en |
dc.identifier.doi | 10.1093/annonc/mdw611 | - |
dc.identifier.pmid | 28426106 | - |
dc.identifier.scopus | 2-s2.0-85015712569 | - |
dc.relation.pages | 270-277 | - |
dc.relation.journalvolume | 28 | - |
dc.relation.journalissue | 2 | - |
item.fulltext | no fulltext | - |
item.openairetype | journal article | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.grantfulltext | none | - |
item.cerifentitytype | Publications | - |
crisitem.author.dept | Oncology | - |
crisitem.author.dept | Cancer Administration and Coordination Center | - |
crisitem.author.dept | National Taiwan University Cancer Center (NTUCC) | - |
crisitem.author.orcid | 0000-0002-5586-5138 | - |
crisitem.author.parentorg | College of Medicine | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
crisitem.author.parentorg | National Taiwan University Hospital | - |
顯示於: | 腫瘤醫學研究所 |
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