Please use this identifier to cite or link to this item: https://repository.monashhealth.org/monashhealthjspui/handle/1/56839
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dc.contributor.authorDavid S.-
dc.coverage.spatialMonash Medical Centre-
dc.date.accessioned2025-12-23T22:38:51Z-
dc.date.available2025-12-23T22:38:51Z-
dc.date.issued2020-11-16-
dc.identifier.urihttps://repository.monashhealth.org/monashhealthjspui/handle/1/56839-
dc.description.abstractWho is it for? This study will investigate the safety and efficacy of Stereotactic Radiotherapy treatment in combination with aromatase inhibitor and cyclin-dependent kinase (CDK) 4/6 inhibitor for metastatic breast cancer." You may be eligible to join this study if you are aged 18 and above, have histologically proven ER-positive, HER2-negative advanced breast cancer with metastases and receiving an aromatase inhibitor in combination with a CDK 4/6 inhibitor Study details All participants in this study receive stereotactic radiotherapy (between 1 -5 doses as ascertained by treating Doctor after consultation) in combination with prescribed aromatase inhibitor and CDK 4/6 inhibitor. Participants will be monitored for reactions and treatment effectiveness, and provide blood and urine for analysis throughout the 2 year study. This research will give us information about whether adding radiotherapy to a CDK 4/6 inhibitor increases the amount of time participants can stay on CDK 4/6 inhibitor therapy.-
dc.titleStereotactic Radiotherapy for Oligoprogressive ER-positive Breast Cancer. AVATAR.-
dc.typeClinical trial-
dc.description.publicationstatusNot Applicable-
dc.identifier.urlhttps://www.anzctr.org.au/Trial/Registration/TrialReview.aspx?id=380294-
dc.identifier.externalACTRN12620001212943-
item.openairetypeClinical trial-
item.fulltextNo Fulltext-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptOncology-
Appears in Collections:Clinical Trials
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