https://scholars.lib.ntu.edu.tw/handle/123456789/494954
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Wu Y.-L | en_US |
dc.contributor.author | Saijo N | en_US |
dc.contributor.author | Thongprasert S | en_US |
dc.contributor.author | CHIH-HSIN YANG | en_US |
dc.contributor.author | Han B | en_US |
dc.contributor.author | Margono B | en_US |
dc.contributor.author | Chewaskulyong B | en_US |
dc.contributor.author | Sunpaweravong P | en_US |
dc.contributor.author | Ohe Y | en_US |
dc.contributor.author | Ichinose Y | en_US |
dc.contributor.author | Yang J.-J | en_US |
dc.contributor.author | Mok T.S.K | en_US |
dc.contributor.author | Young H | en_US |
dc.contributor.author | Haddad V | en_US |
dc.contributor.author | Rukazenkov Y | en_US |
dc.contributor.author | Fukuoka M. | en_US |
dc.creator | Wu Y.-L;Saijo N;Thongprasert S;Chih-Hsin Yang;Han B;Margono B;Chewaskulyong B;Sunpaweravong P;Ohe Y;Ichinose Y;Yang J.-J;Mok T.S.K;Young H;Haddad V;Rukazenkov Y;Fukuoka M. | - |
dc.date.accessioned | 2020-05-26T09:26:40Z | - |
dc.date.available | 2020-05-26T09:26:40Z | - |
dc.date.issued | 2017 | - |
dc.identifier.issn | 0169-5002 | - |
dc.identifier.uri | https://www.scopus.com/inward/record.uri?eid=2-s2.0-85009789298&doi=10.1016%2fj.lungcan.2016.11.022&partnerID=40&md5=4251f94508ee6fd7315f0dce47fe1959 | - |
dc.identifier.uri | https://scholars.lib.ntu.edu.tw/handle/123456789/494954 | - |
dc.description.abstract | Objective The Phase III, randomized, open-label IPASS study (NCT00322452) of first-line epidermal growth factor receptor tyrosine kinase inhibitor (EGFR TKI) gefitinib versus carboplatin/paclitaxel for Asian patients with advanced non-small-cell lung cancer (NSCLC) showed that investigator-assessed progression-free survival (PFS) and objective response rate (ORR) were significantly prolonged in patients with EGFR mutation-positive NSCLC who received gefitinib versus patients with EGFR mutation-negative NSCLC. We report post-hoc analyses of IPASS data by blind independent central review (BICR), performed at the request of the US FDA, in a subset of patients with EGFR mutation-positive NSCLC. Patients and methods Eligible patients (aged ?18 years; histologically/cytologically confirmed Stage IIB/IV adenocarcinoma NSCLC; non- or former light-smokers; treatment-na?ve) were randomly assigned 1:1 to gefitinib (250 mg/day) or carboplatin (dose calculated to produce an area under the curve of 5 or 6 mg/mL/minute)/paclitaxel (200 mg/m2). Primary endpoint: PFS. BICR analyses included PFS, ORR, and duration of response (DoR). Results Scans from 186 IPASS patients (gefitinib n = 88, carboplatin/paclitaxel n = 98) with EGFR mutation-positive NSCLC were available for BICR. Consistent with investigator-assessed results, in patients with EGFR mutation-positive NSCLC: PFS (hazard ratio 0.54; 95% confidence interval [CI] 0.38, 0.79; p = 0.0012) and ORR (odds ratio 3.00; 95% CI 1.63, 5.54; p = 0.0004) were significantly longer with gefitinib versus carboplatin/paclitaxel. The median DoR by BICR was 9.6 months with gefitinib and 5.5 months with carboplatin/paclitaxel. Conclusion BICR analysis of IPASS data support the original, investigator-assessed results. EGFR mutation-positive status remains a significant predictor of response to first-line TKI therapy. ? 2016 The Authors | - |
dc.publisher | Elsevier Ireland Ltd | - |
dc.relation.ispartof | Lung Cancer | - |
dc.subject | Epidermal growth factor receptor tyrosine kinase inhibitor; Epidermal growth factor receptor-mutation positive; IPASS study; Non-small-cell lung cancer | - |
dc.subject.classification | [SDGs]SDG3 | - |
dc.subject.other | carboplatin; epidermal growth factor receptor; gefitinib; paclitaxel; antineoplastic agent; carboplatin; epidermal growth factor receptor; gefitinib; paclitaxel; protein kinase inhibitor; quinazoline derivative; adult; advanced cancer; aged; Article; Asian; cancer combination chemotherapy; cancer staging; cancer survival; drug efficacy; female; food and drug administration; gene mutation; histopathology; human; lung adenocarcinoma; major clinical study; male; multicenter study (topic); multiple cycle treatment; open study; phase 3 clinical trial (topic); post hoc analysis; priority journal; progression free survival; randomized controlled trial (topic); smoking; treatment response; adenocarcinoma; Asian continental ancestry group; Carcinoma, Non-Small-Cell Lung; clinical trial; disease free survival; epidemiology; genetics; Lung Neoplasms; middle aged; multicenter study; mutation; pathology; phase 3 clinical trial; very elderly; Adenocarcinoma; Aged; Aged, 80 and over; Antineoplastic Agents; Antineoplastic Combined Chemotherapy Protocols; Asian Continental Ancestry Group; Carboplatin; Carcinoma, Non-Small-Cell Lung; Disease-Free Survival; Female; Humans; Lung Neoplasms; Male; Middle Aged; Mutation; Neoplasm Staging; Paclitaxel; Protein Kinase Inhibitors; Quinazolines; Randomized Controlled Trials as Topic; Receptor, Epidermal Growth Factor; Smoking | - |
dc.title | Efficacy according to blind independent central review: Post-hoc analyses from the phase III, randomized, multicenter, IPASS study of first-line gefitinib versus carboplatin/paclitaxel in Asian patients with EGFR mutation-positive advanced NSCLC | en_US |
dc.type | journal article | en |
dc.identifier.doi | 10.1016/j.lungcan.2016.11.022 | - |
dc.identifier.pmid | 28212993 | - |
dc.identifier.scopus | 2-s2.0-85009789298 | - |
dc.relation.pages | 119-125 | - |
dc.relation.journalvolume | 104 | - |
item.fulltext | no fulltext | - |
item.openairecristype | http://purl.org/coar/resource_type/c_6501 | - |
item.cerifentitytype | Publications | - |
item.openairetype | journal article | - |
item.grantfulltext | none | - |
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 |
在 IR 系統中的文件,除了特別指名其著作權條款之外,均受到著作權保護,並且保留所有的權利。