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
dc.contributor.author | Chan, Arlene | |
dc.contributor.author | McGregor, S. | |
dc.contributor.author | Liang, Wenbin | |
dc.date.accessioned | 2017-01-30T14:40:36Z | |
dc.date.available | 2017-01-30T14:40:36Z | |
dc.date.created | 2015-01-18T20:00:35Z | |
dc.date.issued | 2014 | |
dc.identifier.citation | Chan, 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.uri | http://hdl.handle.net/20.500.11937/40229 | |
dc.identifier.doi | 10.1016/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.publisher | Churchill Livingstone | |
dc.subject | Relative dose intensity | |
dc.subject | First cycle nadir | |
dc.subject | Breast cancer | |
dc.subject | G-CSF use | |
dc.title | 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 | |
dc.type | Journal Article | |
dcterms.source.volume | 23 | |
dcterms.source.startPage | 676 | |
dcterms.source.endPage | 682 | |
dcterms.source.issn | 09609776 | |
dcterms.source.title | The Breast | |
curtin.department | National Drug Research Institute (NDRI) | |
curtin.accessStatus | Fulltext not available |