Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/27950
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dc.contributor.authorWu, Yi-Long-
dc.contributor.authorTsuboi, Masahiro-
dc.contributor.authorJohn, Thomas-
dc.contributor.authorGrohe, Christian-
dc.contributor.authorMajem, Margarita-
dc.contributor.authorGoldman, Jonathan W-
dc.contributor.authorLaktionov, Konstantin-
dc.contributor.authorKim, Sang-We-
dc.contributor.authorKato, Terufumi-
dc.contributor.authorVu, Huu-Vinh-
dc.contributor.authorLu, Shun-
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.authorZeng, Lingmin-
dc.contributor.authorHodge, Rachel-
dc.contributor.authorAtasoy, Ajlan-
dc.contributor.authorRukazenkov, Yuri-
dc.contributor.authorHerbst, Roy S-
dc.date2021-11-01-
dc.date.accessioned2021-11-08T23:22:52Z-
dc.date.available2021-11-08T23:22:52Z-
dc.date.issued2021-12-01-
dc.identifier.citationFuture Oncology 2021; 17(35): 4827-4835en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/27950-
dc.description.abstractHere, we summarize the initial results from the ADAURA clinical study looking at treatment with osimertinib in patients with a specific type of non-small cell lung cancer (also called NSCLC). Osimertinib (TAGRISSO®) is a medication used to treat a type of NSCLC with a change (mutation) in the EGFR gene, known as EGFR-mutated NSCLC. EGFR stands for 'epidermal growth factor receptor'. It is a protein present on the surface of both healthy and cancer cells that can regulate how cells grow and divide. Sometimes, certain mutations in EGFR can result in the EGFR protein malfunctioning, which can lead to the formation of cancer, like EGFR-mutated NSCLC. Based on previous clinical studies, osimertinib is already approved for use in patients with EGFR-mutated NSCLC that has spread beyond the lung (metastatic disease). This medication works to stop, prevent, or slow the growth of EGFR-mutated NSCLC tumors, by specifically blocking the activity of EGFR. In the ADAURA clinical study, participants had resectable EGFR-mutated NSCLC, which means they had tumors that can be removed by surgery. Participants took either osimertinib or a placebo (a dummy drug with no active ingredient) after having their tumors removed by surgery. Post-surgery chemotherapy was allowed, but not compulsory (this was decided by the participant and their doctor). To date, the study has shown that osimertinib could be beneficial for patients with resectable EGFR-mutated NSCLC. Participants who took osimertinib have stayed cancer-free for longer than those who took the placebo, regardless of whether or not they received chemotherapy after surgery. Osimertinib treatment also reduced the risk of tumors spreading to the brain and spinal cord, otherwise known as the central nervous system (also called CNS). The side effects experienced by the participants taking osimertinib have been consistent with what we already know. Based on the results from ADAURA, osimertinib has been approved for the treatment of resectable EGFR-mutated NSCLC after tumor removal. The ADAURA study is still ongoing and more results are expected to be released in the future. ClinicalTrials.gov NCT number: NCT02511106.en
dc.language.isoeng-
dc.subjectCNS metastasesen
dc.subjectChemotherapyen
dc.subjectEGFR gene mutationen
dc.subjectLay summaryen
dc.subjectNon-small cell lung canceren
dc.subjectOsimertiniben
dc.subjectPlain language summaryen
dc.subjectSurgeryen
dc.titleA plain language summary of results from the ADAURA study: osimertinib after surgery for patients who have early-stage EGFR-mutated non-small cell lung cancer.en
dc.typeJournal Articleen
dc.identifier.journaltitleFuture Oncologyen
dc.identifier.affiliationDepartment of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spain..en
dc.identifier.affiliationMedical Oncology, Yale School of Medicine and Yale Cancer Center, New Haven, CT, USAen
dc.identifier.affiliationDepartment of Respiratory Diseases, Evangelische Lungenklinik, Berlin, Germanyen
dc.identifier.affiliationGuangdong Lung Cancer Institute, Guangdong Provincial People's Hospital and Guangdong Academy of Medical Sciences, Guangzhou, China..en
dc.identifier.affiliationMedical Oncologyen
dc.identifier.affiliationLate Oncology Statistics, AstraZeneca, Cambridge, UKen
dc.identifier.affiliationLate Oncology Research & Development, AstraZeneca, Cambridge, UKen
dc.identifier.affiliationDavid Geffen School of Medicine at University of California Los Angeles, CA, USAen
dc.identifier.affiliationLate Oncology Statistics, AstraZeneca, Gaithersburg, MD, USAen
dc.identifier.affiliationDepartment of Thoracic Surgery and Oncology, National Cancer Center Hospital East, Kashiwa, Japanen
dc.identifier.affiliationDepartment of Medical Oncology, Hospital de la Santa Creu i Sant Pau, Barcelona, Spainen
dc.identifier.affiliationCenter of Innovative Technologies and Oncology, N.N. Blokhin Russian Cancer Center, Russian Academy of Medical Sciences, Moscow, Russiaen
dc.identifier.affiliationDepartment of Oncology, Asan Medical Center, University of Ulsan College of Medicine, Seoul, South Koreaen
dc.identifier.affiliationDepartment of Thoracic Oncology, Kanagawa Cancer Center, Yokohama, Japanen
dc.identifier.affiliationDepartment of Thoracic Surgery, Choray Hospital, Ho Chi Minh City, Vietnamen
dc.identifier.affiliationLung Cancer Center, Shanghai Chest Hospital, Shanghai Jiao Tong University, Shanghai, Chinaen
dc.identifier.affiliationPrecision Medicine, Lung Cancer Center, Konkuk University Medical Center, Seoul, South Koreaen
dc.identifier.affiliationDivision of Medical Oncology, Faculty of Medicine, Siriraj Hospital, Bangkok, Thailanden
dc.identifier.affiliationDepartment of Internal Medicine, National Taiwan University Hospital Hsinchu Branch and National Taiwan University College of Medicine, Taipei, Taiwanen
dc.identifier.affiliationThoracic Oncology Division, European Institute of Oncology (IEO), IRCCS, Milan, Italyen
dc.identifier.affiliationMedical Oncology 2, Istituto Oncologico Veneto IOV IRCCS, Padova, Italyen
dc.identifier.affiliationInstituto de Investigacion Sanitaria-Fundacion de la Jimenez Diaz, Madrid, Spainen
dc.identifier.affiliationDepartment of Medical Oncology and Hematology, University Health Network, Princess Margaret Hospital and the University of Toronto, Toronto, Ontario, Canadaen
dc.identifier.doi10.2217/fon-2021-0752en
dc.type.contentTexten
dc.identifier.pubmedid34723634-
local.name.researcherJohn, Thomas
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.languageiso639-1en-
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
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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