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dc.contributor.authorSaw, RP-M
dc.contributor.authorArmstrong, B
dc.contributor.authorMason, RS
dc.contributor.authorMorton, RL
dc.contributor.authorShannon, KF
dc.contributor.authorSpillane, AJ
dc.contributor.authorStretch, JR
dc.contributor.authorThompson, JF
dc.date.accessioned2022-08-23T01:43:00Z
dc.date.available2022-08-23T01:43:00Z
dc.date.issued2014en_AU
dc.identifier.urihttps://hdl.handle.net/2123/29440
dc.description.abstractPatients with primary cutaneous melanomas that are ulcerated and >2 mm in thickness, >4 mm in thickness and those with nodal micrometastases at diagnosis, have few options for adjuvant treatment. Recent studies have suggested a role for vitamin D to delay melanoma recurrence and improve overall prognosis.en_AU
dc.language.isoenen_AU
dc.publisherBMC Canceren_AU
dc.rightsCreative Commons Attribution 4.0en_AU
dc.subjectmelanomaen_AU
dc.subjectrandomised trialen_AU
dc.subjectvitamin Den_AU
dc.subjectsafetyen_AU
dc.subjecttoxicityen_AU
dc.subjectrecurrenceen_AU
dc.titleAdjuvant therapy with high dose vitamin D following primary treatment of melanoma at high risk of recurrence: A placebo controlled randomised phase II trial (ANZMTG 02.09 Mel-D)en_AU
dc.typeArticleen_AU
dc.subject.asrc1117 Public Health and Health Servicesen_AU
dc.identifier.doi10.1186/1471-2407-14-780
dc.type.pubtypePublisher's versionen_AU
usyd.facultySeS faculties schools::Faculty of Medicine and Health::NHMRC Clinical Trials Centreen_AU
workflow.metadata.onlyNoen_AU


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