Abstract
In 2007 docetaxel was introduced as part of the adjuvant setting offered to high risk breast cancer patients in Denmark. Meta-analyses had shown that taxane-containing chemotherapy reduced the relative risk of relapse and death by 20-30%, apparently with moderate side effects. The treatment was given as three cycles of cyclophosphamide (600 mg/m(2)) and epirubicin (90 mg/m(2)) followed by three cycles of docetaxel (100 mg/m(2)). Because of an apparent high incidence of side effects, especially febrile neutropenia (FN) and non-hematologic side effects, the DBCG (The Danish Breast Cancer Cooperative Group) initiated a retrospective study of adverse reactions to the newly introduced regime and all patients were offered primary prophylaxis with growth factors (G-CSF) pr 1/1-2008.
Originalsprog | Engelsk |
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Tidsskrift | Acta Oncologica |
Vol/bind | 50 |
Udgave nummer | 7 |
Sider (fra-til) | 1075-82 |
Antal sider | 8 |
ISSN | 0284-186X |
DOI | |
Status | Udgivet - okt. 2011 |