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DC Field | Value | Language |
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dc.contributor.author | Tan, L. | - |
dc.contributor.author | Brown, C. | - |
dc.contributor.author | Mersiades, A. | - |
dc.contributor.author | Lee, C. K. | - |
dc.contributor.author | John, T. | - |
dc.contributor.author | Kao, S. | - |
dc.contributor.author | Newnham, G. | - |
dc.contributor.author | O?Byrne, K. | - |
dc.contributor.author | Parakh, S. | - |
dc.contributor.author | Bray, V. | - |
dc.contributor.author | Jasas, K. | - |
dc.contributor.author | Yip, S. | - |
dc.contributor.author | Wong, S. Q. | - |
dc.contributor.author | Ftouni, S. | - |
dc.contributor.author | Guinto, J. | - |
dc.contributor.author | Chandrashekar, S. | - |
dc.contributor.author | Clarke, S. | - |
dc.contributor.author | Pavlakis, N. | - |
dc.contributor.author | Stockler, M. R. | - |
dc.contributor.author | Dawson, S. J. | - |
dc.contributor.author | Solomon, B. J. | - |
dc.date.accessioned | 2024-06-03T03:25:29Z | - |
dc.date.available | 2024-06-03T03:25:29Z | - |
dc.date.issued | 2024 | - |
dc.identifier.issn | 20411723 (ISSN) | - |
dc.identifier.uri | https://swslhd.intersearch.com.au/swslhdjspui/handle/1/12692 | - |
dc.description.abstract | In this phase II, single arm trial (ACTRN12617000720314), we investigate if alternating osimertinib and gefitinib would delay the development of resistance to osimertinib in advanced, non-small cell lung cancer (NSCLC) with the epidermal growth factor receptor (EGFR) T790M mutation (n = 47) by modulating selective pressure on resistant clones. The primary endpoint is progression free-survival (PFS) rate at 12 months, and secondary endpoints include: feasibility of alternating therapy, overall response rate (ORR), overall survival (OS), and safety. The 12-month PFS rate is 38% (95% CI 27.5?55), not meeting the pre-specified primary endpoint. Serial circulating tumor DNA (ctDNA) analysis reveals decrease and clearance of the original activating EGFR and EGFR-T790M mutations which are prognostic of clinical outcomes. In 73% of participants, loss of T790M ctDNA is observed at progression and no participants have evidence of the EGFR C797S resistance mutation following the alternating regimen. These findings highlight the challenges of treatment strategies designed to modulate clonal evolution and the clinical importance of resistance mechanisms beyond suppression of selected genetic mutations in driving therapeutic escape to highly potent targeted therapies. � The Author(s) 2024. | - |
dc.publisher | Nature Research | - |
dc.subject | Acrylamides Aniline Compounds Carcinoma, Non-Small-Cell Lung ErbB Receptors Gefitinib Humans Indoles Lung Neoplasms Mutation Protein Kinase Inhibitors Pyrimidines chloroplast DNA circulating tumor DNA epidermal growth factor receptor osimertinib acrylamide derivative aniline derivative EGFR protein, human indole derivative protein kinase inhibitor pyrimidine derivative cancer cell component DNA fingerprinting survival tumor adult Article backache cancer combination chemotherapy clinical article clinical outcome clonal evolution connective tissue disease coughing diarrhea droplet digital polymerase chain reaction drug safety ECOG Performance Status exon fatigue female gene mutation genomic mutation headache human interstitial lung disease Kaplan Meier method log rank test male metastasis nausea non small cell lung cancer overall response rate overall survival pain people by smoking status progression free survival rash small cell lung cancer clinical trial genetics lung tumor pathology phase 2 clinical trial | - |
dc.title | A Phase II trial of alternating osimertinib and gefitinib therapy in advanced EGFR-T790M positive non-small cell lung cancer: OSCILLATE | - |
dc.type | Journal Article | - |
dc.contributor.swslhdauthor | Bray, Victoria J. | - |
dc.description.affiliates | Peter MacCallum Cancer Centre, Melbourne, VIC, Australia Sir Peter MacCallum Department of Oncology, The University of Melbourne, Melbourne, VIC, Australia NHMRC Clinical Trials Centre, University of Sydney, Sydney, NSW, Australia St George Hospital, Sydney, NSW, Australia Chris O?Brien Lifehouse, Sydney, NSW, Australia St Vincent?s Hospital, Melbourne, VIC, Australia Princess Alexandra Hospital, Brisbane, QLD, Australia Austin Hospital, Olivia Newton John Cancer and Wellness and Research Centre, Melbourne, VIC, Australia Liverpool Hospital, Sydney, NSW, Australia Sir Charles Gairdner Hospital, Perth, WA, Australia Royal North Shore Hospital, Sydney, NSW, Australia University of Sydney, Sydney, NSW, Australia Centre for Cancer Research, The University of Melbourne, Melbourne, VIC, Australia | - |
dc.identifier.doi | 10.1038/s41467-024-46008-1 | - |
dc.identifier.department | Liverpool Hospital, Cancer Therapy Centre | - |
dc.type.studyortrial | Article | - |
dc.identifier.journaltitle | Nature Communications | - |
Appears in Collections: | Liverpool Hospital |
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