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dc.contributor.authorChan, Arlene
dc.contributor.authorMcGregor, S.
dc.contributor.authorLiang, Wenbin
dc.date.accessioned2017-01-30T14:40:36Z
dc.date.available2017-01-30T14:40:36Z
dc.date.created2015-01-18T20:00:35Z
dc.date.issued2014
dc.identifier.citationChan, A. and McGregor, S. and Liang, W. 2014. Utilisation of primary and secondary G-CSF prophylaxis enables maintenance of optimal dose delivery of standard adjuvant chemotherapy for early breast cancer: An analysis of 1655 patients. The Breast. 23 (5): pp. 676-682.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/40229
dc.identifier.doi10.1016/j.breast.2014.07.004
dc.description.abstract

Optimal outcome for early breast cancer patients receiving adjuvant chemotherapy requires adequate dose delivery, commonly defined as >85% of planned dose of chemotherapy agents. Outside the clinical trial setting, reports from community oncology centres have demonstrated that a significant proportion of patients fail to receive this dose intensity, with neutropenia being the most commonly cited reason for sub-optimal treatment. Data collected prospectively on 1655 patient treated in a single breast cancer centre demonstrates that patients at risk of sub-optimal dose delivery can be identified by routine assessment of neutropenic events during the first cycle. The uniform administration of secondary G-CSF for all subsequent cycles enables dose delivery ≥85%, which was shown to lead to improved survival outcomes when compared with those patients who received <85%.

dc.publisherChurchill Livingstone
dc.subjectRelative dose intensity
dc.subjectFirst cycle nadir
dc.subjectBreast cancer
dc.subjectG-CSF use
dc.titleUtilisation of primary and secondary G-CSF prophylaxis enables maintenance of optimal dose delivery of standard adjuvant chemotherapy for early breast cancer: An analysis of 1655 patients
dc.typeJournal Article
dcterms.source.volume23
dcterms.source.startPage676
dcterms.source.endPage682
dcterms.source.issn09609776
dcterms.source.titleThe Breast
curtin.departmentNational Drug Research Institute (NDRI)
curtin.accessStatusFulltext not available


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