Patient-Reported Symptoms and Impact of Treatment With Osimertinib Versus Chemotherapy in Advanced Non-Small-Cell Lung Cancer: The AURA3 Trial

被引:31
作者
Lee, Chee Khoon [1 ]
Novello, Silvia [2 ]
Ryden, Anna [3 ]
Mann, Helen [4 ]
Mok, Tony [5 ]
机构
[1] St George Hosp, Kogarah, NSW, Australia
[2] Univ Turin, Turin, Italy
[3] AstraZeneca Gothenburg, Molndal, Sweden
[4] AstraZeneca R&D, Cambridge, England
[5] Chinese Univ Hong Kong, Prince Wales Hosp, Hong Kong, Hong Kong, Peoples R China
关键词
QUALITY-OF-LIFE; MINIMAL IMPORTANT DIFFERENCES; EORTC QLQ-C30; EUROPEAN-ORGANIZATION; 1ST-LINE TREATMENT; OPEN-LABEL; PHASE-III; EGFR-TKI; T790M MUTATION; CLINICAL-TRIAL;
D O I
10.1200/JCO.2017.77.2293
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
PurposeCapturing patient-reported outcome data is important for evaluating the overall clinical benefits of new cancer therapeutics. We assessed self-reported symptoms of advanced non-small-cell lung cancer in patients treated with osimertinib or chemotherapy in the AURA3 phase III trial.Patients and MethodsPatients completed the European Organisation for Research and Treatment of Cancer 13-item Quality of Life Questionnaire-Lung Cancer Module (EORTC QLQ-LC13) questionnaire on disease-specific symptoms and the EORTC 30-item Core Quality of Life Questionnaire (EORTC QLC-C30) on general cancer symptoms, functioning, global health status/quality of life. We assessed differences between treatments in time to deterioration of individual symptoms and odds of improvement (a deterioration or improvement was defined as a change in score from baseline of 10). Hazard ratios (HRs) were calculated using a log-rank test stratified by ethnicity; odds ratios (ORs) were assessed using logistic regression adjusted for ethnicity.ResultsAt baseline, the questionnaires were completed by 82% to 88% of patients, and 30% to 70% had individual key symptoms. Time to deterioration was longer with osimertinib than with chemotherapy for cough (HR, 0.74; 95% CI, 0.53 to 1.05), chest pain (HR, 0.52; 95% CI, 0.37 to 0.73), and dyspnea (HR, 0.42; 95% CI, 0.31 to 0.58). The proportion of symptomatic patients with improvement in global health status/quality of life was higher with osimertinib (80 [37%] of 215) than with chemotherapy (23 [22%] of 105; OR, 2.11; 95% CI, 1.24 to 3.67; P = .007). Proportions were also higher for appetite loss (OR, 2.50; 95% CI, 1.31 to 4.84) and fatigue (OR, 1.96; 95% CI, 1.20 to 3.22).ConclusionTime to deterioration of key symptoms was longer with osimertinib than with chemotherapy, and a higher proportion of patients had improvement in global health status/quality of life, demonstrating improved patient outcomes with osimertinib.
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收藏
页码:1853 / +
页数:14
相关论文
共 50 条
[1]   THE EUROPEAN-ORGANIZATION-FOR-RESEARCH-AND-TREATMENT-OF-CANCER QLQ-C30 - A QUALITY-OF-LIFE INSTRUMENT FOR USE IN INTERNATIONAL CLINICAL-TRIALS IN ONCOLOGY [J].
AARONSON, NK ;
AHMEDZAI, S ;
BERGMAN, B ;
BULLINGER, M ;
CULL, A ;
DUEZ, NJ ;
FILIBERTI, A ;
FLECHTNER, H ;
FLEISHMAN, SB ;
DEHAES, JCJM ;
KAASA, S ;
KLEE, M ;
OSOBA, D ;
RAZAVI, D ;
ROFE, PB ;
SCHRAUB, S ;
SNEEUW, K ;
SULLIVAN, M ;
TAKEDA, F .
JOURNAL OF THE NATIONAL CANCER INSTITUTE, 1993, 85 (05) :365-376
[2]  
[Anonymous], CHMPEWP20595 EUR MED
[3]  
[Anonymous], 2009, GUID IND PAT OUTC ME
[4]  
[Anonymous], J CLIN ONCOL S
[5]   Preclinical Comparison of Osimertinib with Other EGFR-TKIs in EGFR-Mutant NSCLC Brain Metastases Models, and Early Evidence of Clinical Brain Metastases Activity [J].
Ballard, Peter ;
Yates, James W. T. ;
Yang, Zhenfan ;
Kim, Dong-Wan ;
Yang, James Chih-Hsin ;
Cantarini, Mireille ;
Pickup, Kathryn ;
Jordan, Angela ;
Hickey, Mike ;
Grist, Matthew ;
Box, Matthew ;
Johnstrom, Peter ;
Varnas, Katarina ;
Malmquist, Jonas ;
Thress, Kenneth S. ;
Janne, Pasi A. ;
Cross, Darren .
CLINICAL CANCER RESEARCH, 2016, 22 (20) :5130-5140
[6]   Recommendations for Incorporating Patient-Reported Outcomes Into Clinical Comparative Effectiveness Research in Adult Oncology [J].
Basch, Ethan ;
Abernethy, Amy P. ;
Mullins, C. Daniel ;
Reeve, Bryce B. ;
Smith, Mary Lou ;
Coons, Stephen Joel ;
Sloan, Jeff ;
Wenzel, Keith ;
Chauhan, Cynthia ;
Eppard, Wayland ;
Frank, Elizabeth S. ;
Lipscomb, Joseph ;
Raymond, Stephen A. ;
Spencer, Merianne ;
Tunis, Sean .
JOURNAL OF CLINICAL ONCOLOGY, 2012, 30 (34) :4249-4255
[7]   Minimal important differences in the EORTC QLQ-C30 in patients with advanced cancer [J].
Bedard, Gillian ;
Zeng, Liang ;
Zhang, Liying ;
Lauzon, Natalie ;
Holden, Lori ;
Tsao, May ;
Danjoux, Cyril ;
Barnes, Elizabeth ;
Sahgal, Arjun ;
Poon, Michael ;
Chow, Edward .
ASIA-PACIFIC JOURNAL OF CLINICAL ONCOLOGY, 2014, 10 (02) :109-117
[8]   THE EORTC QLQ-LC13 - A MODULAR SUPPLEMENT TO THE EORTC CORE QUALITY-OF-LIFE QUESTIONNAIRE (QLQ-C30) FOR USE IN LUNG-CANCER CLINICAL-TRIALS [J].
BERGMAN, B ;
AARONSON, NK ;
AHMEDZAI, S ;
KAASA, S ;
SULLIVAN, M .
EUROPEAN JOURNAL OF CANCER, 1994, 30A (05) :635-642
[9]   Factors affecting baseline quality of life in two international adjuvant breast cancer trials [J].
Bernhard, J ;
Hürny, C ;
Coates, AS ;
Peterson, HF ;
Castiglione-Gertsch, M ;
Gelber, RD ;
Galligioni, E ;
Marini, G ;
Thürlimann, B ;
Forbes, JF ;
Goldhirsch, A ;
Senn, HJ ;
Rudenstam, CM .
BRITISH JOURNAL OF CANCER, 1998, 78 (05) :686-693
[10]   Health related quality of life outcomes in cancer clinical trials [J].
Bottomley, A ;
Flechtner, H ;
Efficace, F ;
Vanvoorden, V ;
Coens, C ;
Therasse, P ;
Velikova, G ;
Blazeby, J ;
Greimel , E .
EUROPEAN JOURNAL OF CANCER, 2005, 41 (12) :1697-1709