Department of Medicine I and Clinical Division of Oncology, Medical University of Vienna, Vienna; Central European Cooperative Oncology Group (CECOG), Vienna, Austria.
Department of Medicine, University of Washington, Seattle, WA, USA.
Ann Oncol. 2010 Nov;21(11):2145-2152. doi: 10.1093/annonc/mdq069. Epub 2010 Mar 23.
While 'targeted' drugs often take centre stage when considering developments in breast cancer, improved understanding, administration and use of chemotherapeutic agents also contribute to better outcomes for women with metastatic breast cancer. Moreover, these developments offer the potential for further improvements when chemotherapy and targeted agents are combined. In this article, we focus on capecitabine dosing in advanced breast cancer, review the available data and discuss the implications of this evidence on best treatment practice both for chemotherapy alone and for chemotherapy when combined with biological agents. It appears that a capecitabine starting dose of 1000 mg/m² twice daily enables treatment to be administered for longer periods, providing continuous exposure to cytotoxic therapy and thus prolonging the duration of disease control. Although no randomised data are available comparing different doses of capecitabine, the cumulative evidence supports this approach.
虽然在考虑乳腺癌的发展时,“靶向”药物常常成为焦点,但对化疗药物的理解、管理和使用的改善也有助于转移性乳腺癌女性获得更好的结果。此外,当化疗和靶向药物联合使用时,这些进展为进一步改善提供了潜力。在本文中,我们专注于晚期乳腺癌中卡培他滨的剂量,回顾现有数据,并讨论这一证据对单独化疗和联合生物制剂化疗的最佳治疗实践的影响。似乎卡培他滨的起始剂量为 1000mg/m²,每日两次,可以使治疗持续更长时间,为细胞毒性治疗提供持续暴露,从而延长疾病控制的持续时间。虽然没有比较卡培他滨不同剂量的随机数据,但累积证据支持这种方法。