Cited 60 times in 
Cited 61 times in 
Patient-reported outcomes from FLAURA: Osimertinib versus erlotinib or gefitinib in patients with EGFR-mutated advanced non-small-cell lung cancer
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Leighl, Natasha B. | - |
| dc.contributor.author | Karaseva, Nina | - |
| dc.contributor.author | Nakagawa, Kazuhiko | - |
| dc.contributor.author | Cho, Byoung-Chul | - |
| dc.contributor.author | Gray, Jhanelle E. | - |
| dc.contributor.author | Hovey, Tina | - |
| dc.contributor.author | Walding, Andrew | - |
| dc.contributor.author | Ryden, Anna | - |
| dc.contributor.author | Novello, Silvia | - |
| dc.date.accessioned | 2020-02-11T06:58:19Z | - |
| dc.date.available | 2020-02-11T06:58:19Z | - |
| dc.date.created | 2021-03-17 | - |
| dc.date.issued | 2020-01 | - |
| dc.identifier.issn | 0959-8049 | - |
| dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/174927 | - |
| dc.description.abstract | Background: In the FLAURA trial, osimertinib demonstrated superior progression-free survival and a favorable toxicity profile to erlotinib or gefitinib as initial therapy in patients with EGFR-mutated advanced non-small-cell lung cancer. Patient-reported outcomes from FLAURA are discussed here. Methods: Patients (N = 556) completed the EORTC QLQ-LC13 weekly for 6 weeks, then every 3 weeks, and the QLQ-C30 every 6 weeks. Prespecified key symptoms were cough, dyspnea, chest pain, appetite loss, and fatigue. Score changes from baseline to randomized treatment discontinuation were assessed using a mixed-effects model. A >= 10-point change was considered clinically relevant. Odds of improvement and time to deterioration were investigated. QLQ-C30 functioning scores were assessed post hoc. Results: Questionnaire completion rates were >70% at most time points. Baseline mean scores were similar in the osimertinib and erlotinib/gefitinib arms. Scores improved in both arms, but none reached clinical relevance at 5% significance level. A statistically significant difference favoring osimertinib for chest pain was not clinically relevant (-6.84 vs -3.88; p = 0.021). Odds of improvement and time to deterioration were similar between treatments. In post hoc analyses, improvements favored osimertinib for emotional functioning (8.79 vs 4.91; p = 0.004) and social functioning (7.66 vs 1.74; p < 0.001). Cognitive functioning remained stable with osimertinib but deteriorated with erlotinib/gefitinib (0.03 vs - 3.91; p = 0.005). Conclusions: Key symptoms improved from baseline in both treatment arms in FLAURA. Key symptom improvements that were both statistically significant and clinically relevant were not observed in favor of either treatment arm. (C) 2019 The Authors. Published by Elsevier Ltd. | - |
| dc.description.statementOfResponsibility | open | - |
| dc.language | English | - |
| dc.publisher | Elsevier Science Ltd | - |
| dc.relation.isPartOf | EUROPEAN JOURNAL OF CANCER | - |
| dc.relation.isPartOf | EUROPEAN JOURNAL OF CANCER | - |
| dc.rights | CC BY-NC-ND 2.0 KR | - |
| dc.subject | QUALITY-OF-LIFE | - |
| dc.subject | OPEN-LABEL | - |
| dc.subject | 1ST-LINE TREATMENT | - |
| dc.subject | PHASE-III | - |
| dc.subject | EUROPEAN-ORGANIZATION | - |
| dc.subject | CLINICAL-TRIALS | - |
| dc.subject | SYMPTOM BURDEN | - |
| dc.subject | CHEMOTHERAPY | - |
| dc.subject | AFATINIB | - |
| dc.subject | SURVIVAL | - |
| dc.title | Patient-reported outcomes from FLAURA: Osimertinib versus erlotinib or gefitinib in patients with EGFR-mutated advanced non-small-cell lung cancer | - |
| dc.type | Article | - |
| dc.contributor.college | College of Medicine (의과대학) | - |
| dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
| dc.contributor.googleauthor | Leighl, Natasha B. | - |
| dc.contributor.googleauthor | Karaseva, Nina | - |
| dc.contributor.googleauthor | Nakagawa, Kazuhiko | - |
| dc.contributor.googleauthor | Cho, Byoung-Chul | - |
| dc.contributor.googleauthor | Gray, Jhanelle E. | - |
| dc.contributor.googleauthor | Hovey, Tina | - |
| dc.contributor.googleauthor | Walding, Andrew | - |
| dc.contributor.googleauthor | Ryden, Anna | - |
| dc.contributor.googleauthor | Novello, Silvia | - |
| dc.identifier.doi | 10.1016/j.ejca.2019.11.006 | - |
| dc.relation.journalcode | J00809 | - |
| dc.identifier.eissn | 1879-0852 | - |
| dc.subject.keyword | EORTC QLQ-C30 | - |
| dc.subject.keyword | EORTC QLQ-LC13 | - |
| dc.subject.keyword | Non-small-cell lung cancer | - |
| dc.subject.keyword | Osimertinib | - |
| dc.subject.keyword | Patient-reported outcomes | - |
| dc.contributor.alternativeName | Cho, Byoung Chul | - |
| dc.contributor.affiliatedAuthor | Cho, Byoung-Chul | - |
| dc.identifier.scopusid | 2-s2.0-85076114162 | - |
| dc.identifier.wosid | 000505199600007 | - |
| dc.citation.volume | 125 | - |
| dc.citation.startPage | 49 | - |
| dc.citation.endPage | 57 | - |
| dc.identifier.bibliographicCitation | EUROPEAN JOURNAL OF CANCER, Vol.125 : 49-57, 2020-01 | - |
| dc.identifier.rimsid | 67899 | - |
| dc.type.rims | ART | - |
| dc.description.journalClass | 1 | - |
| dc.description.journalClass | 1 | - |
| dc.subject.keywordAuthor | EORTC QLQ-C30 | - |
| dc.subject.keywordAuthor | EORTC QLQ-LC13 | - |
| dc.subject.keywordAuthor | Non-small-cell lung cancer | - |
| dc.subject.keywordAuthor | Osimertinib | - |
| dc.subject.keywordAuthor | Patient-reported outcomes | - |
| dc.subject.keywordPlus | QUALITY-OF-LIFE | - |
| dc.subject.keywordPlus | OPEN-LABEL | - |
| dc.subject.keywordPlus | 1ST-LINE TREATMENT | - |
| dc.subject.keywordPlus | PHASE-III | - |
| dc.subject.keywordPlus | EUROPEAN-ORGANIZATION | - |
| dc.subject.keywordPlus | CLINICAL-TRIALS | - |
| dc.subject.keywordPlus | SYMPTOM BURDEN | - |
| dc.subject.keywordPlus | CHEMOTHERAPY | - |
| dc.subject.keywordPlus | AFATINIB | - |
| dc.subject.keywordPlus | SURVIVAL | - |
| dc.type.docType | Article | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalWebOfScienceCategory | Oncology | - |
| dc.relation.journalResearchArea | Oncology | - |
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