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dc.contributor.authorSumitra Thongpraserten_US
dc.contributor.authorEmma Duffielden_US
dc.contributor.authorNagahiro Saijoen_US
dc.contributor.authorYi Long Wuen_US
dc.contributor.authorJames Chih Hsin Yangen_US
dc.contributor.authorDa Tong Chuen_US
dc.contributor.authorMeilin Liaoen_US
dc.contributor.authorYuh Min Chenen_US
dc.contributor.authorHan Pin Kuoen_US
dc.contributor.authorShunichi Negoroen_US
dc.contributor.authorKwok Chi Lamen_US
dc.contributor.authorAlison Armouren_US
dc.contributor.authorPatrick Magillen_US
dc.contributor.authorMasahiro Fukuokaen_US
dc.date.accessioned2018-09-04T04:28:17Z-
dc.date.available2018-09-04T04:28:17Z-
dc.date.issued2011-01-01en_US
dc.identifier.issn15561380en_US
dc.identifier.issn15560864en_US
dc.identifier.other2-s2.0-80054882063en_US
dc.identifier.other10.1097/JTO.0b013e31822adaf7en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=80054882063&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/50311-
dc.description.abstractIntroduction: Evaluation of health-related quality-of-life (HRQoL) and symptom improvement were preplanned secondary objectives for the overall population and posthoc analyses for epidermal growth factor receptor (EGFR) mutation-positive/negative subgroups in IPASS. Methods: HRQoL was assessed using the Functional Assessment of Cancer Therapy-Lung (FACT-L) and Trial Outcome Index (TOI); symptom improvement by the Lung Cancer Subscale (LCS). Improvements defined as: 6 or more (FACT-L; TOI), 2 or more (LCS) points increase maintained for 21 or more days. Results: Overall (n = 1151/1217 evaluable), HRQoL improvement rates were significantly greater with gefitinib versus carboplatin/paclitaxel; symptom improvement rates were similar for both treatments. Significantly more patients recorded improvements in HRQoL and symptoms with gefitinib in the EGFR mutation-positive subgroup (n = 259; FACT-L 70.2% versus 44.5%; odds ratio, 3.01 [95% confidence interval, 1.79-5.07]; p < 0.001; TOI 70.2% versus 38.3%; 3.96 [2.33-6.71]; p < 0.001; LCS 75.6% versus 53.9%; 2.70 [1.58-4.62]; p < 0.001), and with carboplatin/paclitaxel in the EGFR mutation-negative subgroup (n = 169; FACT-L 14.6% versus 36.3%; odds ratio, 0.31 [0.15-0.65]; p = 0.002; TOI 12.4% versus 28.8%; 0.35 [0.16-0.79]; p = 0.011; LCS 20.2% versus 47.5%; 0.28 [0.14-0.55]; p < 0.001). Median time-to-worsening (months) FACT-L score was longer with gefitinib versus carboplatin/paclitaxel for the overall population (8.3 versus 2.5) and EGFR mutation-positive subgroup (15.6 versus 3.0), and similar for both treatments in the EGFR mutation-negative subgroup (1.4 versus 1.4). Median time-to-improvement with gefitinib was 8 days in patients with EGFR mutation-positive tumors who improved. Conclusions: HRQoL and symptom endpoints were consistent with efficacy outcomes in IPASS and favored gefitinib in patients with EGFR mutation-positive tumors and carboplatin/paclitaxel in patients with EGFR mutation-negative tumors. Copyright © 2011 by the International Association for the Study of Lung Cancer.en_US
dc.subjectMedicineen_US
dc.titleHealth-related quality-of-life in a randomized phase III first-line study of gefitinib versus carboplatin/paclitaxel in clinically selected patients from Asia with advanced NSCLC (IPASS)en_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Thoracic Oncologyen_US
article.volume6en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsAstraZenecaen_US
article.stream.affiliationsKindai University School of Medicineen_US
article.stream.affiliationsGuangdong General Hospitalen_US
article.stream.affiliationsNational Taiwan University Hospitalen_US
article.stream.affiliationsBeijing Cancer Hospitalen_US
article.stream.affiliationsShanghai Chest Hospitalen_US
article.stream.affiliationsNational Yang-Ming University Taiwanen_US
article.stream.affiliationsChang Gung Memorial Hospitalen_US
article.stream.affiliationsHyogo Cancer Centeren_US
article.stream.affiliationsPrince of Wales Hospital Hong Kongen_US
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