© 2005 European Society for Medical Oncology
Original article |
Evaluation of anemia, neutropenia and skin toxicities in standard or dose-dense doxorubicin/cyclophosphamide (AC)paclitaxel or docetaxel adjuvant chemotherapy in breast cancer
Hospital of the University of Pennsylvania, Philadelphia, PA, USA
* Correspondence to: Dr J. Schwartz, Women and Infants Hospital, 101 Dudley Street, Providence, RI 02905, USA. Tel: +1-401-274-1122; Email: jschwartz{at}wihri.org
Background: Results of CALGB 9741 demonstrated that administering standard doxorubicin/cyclophosphamide (AC)paclitaxel therapy for adjuvant therapy of breast cancer in a dose-dense fashion with colony-stimulating factors increases efficacy, decreases severe neutropenia, but may increase the need for blood transfusions. A chart review was performed to evaluate the rates of anemia, neutropenia and skin toxicities with dose-dense and traditional ACtaxane chemotherapy.
Patients and methods: A total of 112 patients received one of four treatments: non-dose-dense ACpaclitaxel (NDD Pac), dose-dense ACpaclitaxel (DD Pac), non dose-dense ACdocetaxel (NDD Doc), or dose-dense ACdocetaxel (DD Doc).
Results: Transfusion rates were not increased in the dose-dense population; however, rates of grade 24 anemia (23% versus 0%, P=0.029), as well as erythropoietin use (58% versus 0%, P <0.0001), were significantly increased in the DD Pac group compared with the NDD Pac group. Grade 3 skin toxicities were significantly increased in the DD Doc group compared with the NDD Doc group (70% versus 11%, P <0.0001).
Conclusions: These results demonstrate that dose-dense ACtaxane therapy may increase rates of anemia and the need for erythropoietin, and decrease rates of neutropenia. The utility of DD Doc appears limited by skin toxicities and its use outside of a clinical study should not be recommended.
Key words: anemia, breast cancer, docetaxel, dose-dense, doxorubicin, erythropoietin, handfoot syndrome, neuropathy, paclitaxel
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