A plain language review of results from the LAURA study: osimertinib after chemoradiotherapy for patients with EGFR-mutated non-small cell lung cancer that cannot be removed by surgery

dc.contributor.authorLu S.
dc.contributor.authorKato T.
dc.contributor.authorDong X.
dc.contributor.authorAhn M.J.
dc.contributor.authorQuang L.V.
dc.contributor.authorSoparattanapaisarn N.
dc.contributor.authorInoue T.
dc.contributor.authorWang C.L.
dc.contributor.authorHuang M.
dc.contributor.authorYang J.C.H.
dc.contributor.authorCobo M.
dc.contributor.authorÖzgüroğlu M.
dc.contributor.authorCasarini I.
dc.contributor.authorSriuranpong V.
dc.contributor.authorCronemberger E.
dc.contributor.authorTakahashi T.
dc.contributor.authorRunglodvatana Y.
dc.contributor.authorChen M.
dc.contributor.authorHuang X.
dc.contributor.authorGrainger E.
dc.contributor.authorGhiorghiu D.
dc.contributor.authorvan der Gronde T.
dc.contributor.authorRamalingam S.S.
dc.contributor.correspondenceLu S.
dc.contributor.otherMahidol University
dc.date.accessioned2026-05-16T18:18:23Z
dc.date.available2026-05-16T18:18:23Z
dc.date.issued2026-01-01
dc.description.abstractPlain Language Summary: What is this summary about? We review current standard treatment for patients with non-small cell lung cancer (NSCLC) that has spread to nearby tissues and/or nearby parts of the immune system called lymph nodes (stage III) that could not be removed by surgery (unresectable), and had an EGFR mutation. The epidermal growth factor receptor (known as EGFR) is a type of protein present on the surface of some cells, which controls how cells grow and divide. Mutations in the EGFR gene can result in the development of lung cancer. We include a summary of results from the LAURA study, which evaluated osimertinib treatment for these patients. Osimertinib is a medicine that blocks the activity of mutated EGFR protein on cancer cells, causing cancer cell death and tumor shrinkage. The LAURA study focused on unresectable stage III EGFR-mutated NSCLC treated with chemoradiotherapy (a combination of a medicine and radiation therapy to kill cancer cells and shrink the tumor); if the cancer did not grow or spread during or after this treatment, patients were enrolled in LAURA and randomly assigned to receive osimertinib or placebo. What are the key takeaways? Osimertinib significantly increased the time that patients lived without the cancer growing or spreading (called progression-free survival). Patients who received osimertinib had the median progression-free survival extended by 33.6 months, compared with placebo. The median timepoint of progression-free survival is a type of average at which half of the patients were alive without the cancer growing or spreading. The most common side effects were lung inflammation from radiotherapy (radiation pneumonitis), diarrhea and rash, consistent with what we already know about osimertinib and chemoradiotherapy. What were the main conclusions reported by the researchers? Findings from the LAURA study led to regulatory approvals and guideline recommendations for using osimertinib to treat patients with unresectable stage III EGFR-mutated NSCLC, whose cancer has not grown or spread (progressed) during or after chemoradiotherapy. Clinical trial number: NCT03521154.
dc.identifier.citationFuture Oncology Vol.22 No.11 (2026) , 1247-1262
dc.identifier.doi10.1080/14796694.2026.2652543
dc.identifier.eissn17448301
dc.identifier.issn14796694
dc.identifier.pmid42037107
dc.identifier.scopus2-s2.0-105038027356
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/116746
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.subjectMedicine
dc.titleA plain language review of results from the LAURA study: osimertinib after chemoradiotherapy for patients with EGFR-mutated non-small cell lung cancer that cannot be removed by surgery
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105038027356&origin=inward
oaire.citation.endPage1262
oaire.citation.issue11
oaire.citation.startPage1247
oaire.citation.titleFuture Oncology
oaire.citation.volume22
oairecerif.author.affiliationUniversity of Chinese Academy of Sciences
oairecerif.author.affiliationWest China School of Medicine/West China Hospital of Sichuan University
oairecerif.author.affiliationTongji Medical College of Huazhong University of Science and Technology
oairecerif.author.affiliationNational Taiwan University Hospital
oairecerif.author.affiliationChang Gung University
oairecerif.author.affiliationSamsung Medical Center, Sungkyunkwan university
oairecerif.author.affiliationAstraZeneca
oairecerif.author.affiliationSiriraj Hospital
oairecerif.author.affiliationİstanbul University-Cerrahpaşa Cerrahpaşa Faculty of Medicine
oairecerif.author.affiliationOsaka International Cancer Institute
oairecerif.author.affiliationFaculty of Medicine, Chulalongkorn University
oairecerif.author.affiliationShanghai Chest Hospital
oairecerif.author.affiliationShizuoka Cancer Center
oairecerif.author.affiliationKanagawa Cancer Center Research Institute
oairecerif.author.affiliationHanoi Medical University
oairecerif.author.affiliationVajira Hospital
oairecerif.author.affiliationHospital Municipal Dr. Bernardo A. Houssay
oairecerif.author.affiliationHospitales Universitarios Regional y Virgen de la Victoria
oairecerif.author.affiliationCentro Regional Integrado de Oncologia

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