Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/30298
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dc.contributor.authorMajem, Margarita-
dc.contributor.authorGoldman, Jonathan W-
dc.contributor.authorJohn, Thomas-
dc.contributor.authorGrohe, Christian-
dc.contributor.authorLaktionov, Konstantin-
dc.contributor.authorKim, Sang-We-
dc.contributor.authorKato, Terufumi-
dc.contributor.authorVu, Huu Vinh-
dc.contributor.authorLu, Shun-
dc.contributor.authorLi, Shanqing-
dc.contributor.authorLee, Kye Young-
dc.contributor.authorAkewanlop, Charuwan-
dc.contributor.authorYu, Chong-Jen-
dc.contributor.authorde Marinis, Filippo-
dc.contributor.authorBonanno, Laura-
dc.contributor.authorDomine, Manuel-
dc.contributor.authorShepherd, Frances A-
dc.contributor.authorAtagi, Shinji-
dc.contributor.authorZeng, Lingmin-
dc.contributor.authorKulkarni, Dakshayini-
dc.contributor.authorMedic, Nenad-
dc.contributor.authorTsuboi, Masahiro-
dc.contributor.authorHerbst, Roy S-
dc.contributor.authorWu, Yi-Long-
dc.date.accessioned2022-06-23T00:35:09Z-
dc.date.available2022-06-23T00:35:09Z-
dc.date.issued2022-06-01-
dc.identifier.citationClinical cancer research : an official journal of the American Association for Cancer Research 2022; 28(11): 2286-2296en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/30298-
dc.description.abstractIn the phase III ADAURA trial, adjuvant treatment with osimertinib versus placebo, with/without prior adjuvant chemotherapy, resulted in a statistically significant and clinically meaningful disease-free survival benefit in completely resected stage IB-IIIA EGFR-mutated (EGFRm) non-small cell lung cancer (NSCLC). We report health-related quality of life (HRQoL) outcomes from ADAURA. Patients randomized 1:1 received oral osimertinib 80 mg or placebo for 3 years or until recurrence/discontinuation. HRQoL (secondary endpoint) was measured using the Short Form-36 (SF-36) health survey at baseline, 12, and 24 weeks, then every 24 weeks until recurrence or treatment completion/discontinuation. Exploratory analyses of SF-36 score changes from baseline until week 96 and time to deterioration (TTD) were performed in the overall population (stage IB-IIIA; N = 682). Clinically meaningful changes were defined using the SF-36 manual. Baseline physical/mental component summary (PCS/MCS) scores were comparable between osimertinib and placebo (range, 46-47) and maintained to Week 96, with no clinically meaningful differences between arms; difference in adjusted least squares (LS) mean [95% confidence intervals (CI), -1.18 (-2.02 to -0.34) and -1.34 (-2.40 to -0.28), for PCS and MCS, respectively. There were no differences between arms for TTD of PCS and MCS; HR, 1.17 (95% CI, 0.82-1.67) and HR, 0.98 (95% CI, 0.70-1.39), respectively. HRQoL was maintained with adjuvant osimertinib in patients with stage IB-IIIA EGFRm NSCLC, who were disease-free after complete resection, with no clinically meaningful differences versus placebo, further supporting adjuvant osimertinib as a new treatment in this setting. See related commentary by Patil and Bunn, p. 2204.en
dc.language.isoeng
dc.titleHealth-Related Quality of Life Outcomes in Patients with Resected Epidermal Growth Factor Receptor-Mutated Non-Small Cell Lung Cancer Who Received Adjuvant Osimertinib in the Phase III ADAURA Trial.en
dc.typeJournal Articleen
dc.identifier.journaltitleClinical cancer research : an official journal of the American Association for Cancer Researchen
dc.identifier.affiliationMedical Oncologyen
dc.identifier.affiliationDepartment of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain..en
dc.identifier.affiliationDavid Geffen School of Medicine at University of California Los Angeles, Los Angeles, California..en
dc.identifier.affiliationKlinik für Pneumologie-Evangelische Lungenklinik Berlin Buch, Berlin, Germany..en
dc.identifier.affiliationFederal State Budgetary Institution "N.N.Blokhin National Medical Research Center of Oncology" of the Ministry of Health of the Russian Federation (N.N. Blokhin NMRCO), Moscow, Russia..en
dc.identifier.affiliationDepartment of Oncology, Asan Medical Center, Seoul, South Korea..en
dc.identifier.affiliationDepartment of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japan..en
dc.identifier.affiliationDepartment of Thoracic Surgery, Choray Hospital, Ho Chi Minh City, Vietnam..en
dc.identifier.affiliationLung Cancer Center, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, China..en
dc.identifier.affiliationDepartment of Thoracic Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, Beijing, China..en
dc.identifier.affiliationPrecision Medicine Lung Cancer Center, Konkuk University Medical Center, Seoul, Republic of Korea..en
dc.identifier.affiliationDivision of Medical Oncology, Faculty of Medicine, Siriraj Hospital, Bangkok, Thailand..en
dc.identifier.affiliationDepartment of Internal Medicine, National Taiwan University Hospital Hsinchu Branch and National Taiwan University College of Medicine, Taipei, Taiwan..en
dc.identifier.affiliationThoracic Oncology Division, European Institute of Oncology (IEO), IRCCS, Milan, Italy..en
dc.identifier.affiliationMedical Oncology 2, Istituto Oncologico Veneto (IOV), IRCCS, Padua, Italy..en
dc.identifier.affiliationDepartment of Oncology, Hospital Universitario Fundación Jiménez Díaz (IIS-FJD), Madrid, Spain..en
dc.identifier.affiliationDepartment of Medical Oncology and Hematology, University Health Network, Princess Margaret Cancer Center and the University of Toronto, Toronto, Ontario, Canada..en
dc.identifier.affiliationDepartment of Thoracic Oncology, National Hospital Organization Kinki-Chuo Chest Medical Center, Osaka, Japan..en
dc.identifier.affiliationLate Oncology Statistics, AstraZeneca, Gaithersburg, Maryland..en
dc.identifier.affiliationLate Oncology R&D, AstraZeneca, Cambridge, United Kingdom..en
dc.identifier.affiliationAstraZeneca Oncology Business Unit, Academy House, Cambridge, United Kingdom..en
dc.identifier.affiliationDepartment of Thoracic Surgery and Oncology, National Cancer Center Hospital East, Kashiwa, Japan..en
dc.identifier.affiliationMedical Oncology, Yale School of Medicine and Yale Cancer Center, New Haven, Connecticut..en
dc.identifier.affiliationGuangdong Lung Cancer Institute, Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences, Guangzhou, China..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35012927/en
dc.identifier.doi10.1158/1078-0432.CCR-21-3530en
dc.type.contentTexten
dc.identifier.orcid0000-0002-9919-7485en
dc.identifier.orcid0000-0002-4925-8243en
dc.identifier.orcid0000-0003-3399-5342en
dc.identifier.orcid0000-0003-1065-8095en
dc.identifier.orcid0000-0002-5853-1424en
dc.identifier.orcid0000-0001-6872-2403en
dc.identifier.orcid0000-0003-4687-5593en
dc.identifier.orcid0000-0003-1022-3745en
dc.identifier.orcid0000-0001-5218-4970en
dc.identifier.orcid0000-0002-1128-434Xen
dc.identifier.orcid0000-0003-1876-7069en
dc.identifier.orcid0000-0002-3611-0258en
dc.identifier.pubmedid35012927
local.name.researcherJohn, Thomas
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.openairetypeJournal Article-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.fulltextNo Fulltext-
item.languageiso639-1en-
crisitem.author.deptOlivia Newton-John Cancer Research Institute-
crisitem.author.deptMedical Oncology-
crisitem.author.deptOlivia Newton-John Cancer Wellness and Research Centre-
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