Beatson West of Scotland Cancer Centre, Glasgow, United Kingdom.
Breast Cancer (Dove Med Press). 2009 Aug 31;1:1-18.
Metastatic breast cancer (MBC) remains a major cause of morbidity and mortality in women worldwide. For three decades doxorubicin, alone or in combination with other cytotoxic agents, has been a mainstay of systemic therapy for MBC. However, its use is limited by cumulative cardiotoxicity. More recently liposomal formulations of doxorubicin have been developed which exhibit equal efficacy but reduced cardiotoxicity in comparison to conventional doxorubicin. The novel toxicity profile of liposomal doxorubicins has prompted their evaluation with various cytotoxic agents in patients with MBC. In addition, their favorable cardiac safety profile has prompted re-evaluation of concomitant therapy with doxorubicin and trastuzumab, a regimen of proven efficacy in MBC but previously considered to be associated with significant cardiotoxicity. We review clinical trial data addressing combination therapy with both pegylated and non-pegylated liposomal doxorubicin in patients with MBC.
转移性乳腺癌(MBC)仍然是全世界女性发病率和死亡率的主要原因。三十年来,阿霉素单独或与其他细胞毒性药物联合应用一直是 MBC 系统治疗的主要药物。然而,其应用受到累积性心脏毒性的限制。最近开发了阿霉素的脂质体制剂,与常规阿霉素相比,其疗效相当,但心脏毒性降低。脂质体阿霉素的新型毒性特征促使人们在 MBC 患者中用各种细胞毒性药物对其进行评估。此外,其良好的心脏安全性特征促使人们重新评估阿霉素和曲妥珠单抗的联合治疗,该方案在 MBC 中已被证实有效,但以前认为与显著的心脏毒性相关。我们回顾了临床试验数据,这些数据涉及 MBC 患者中使用聚乙二醇化和非聚乙二醇化脂质体阿霉素的联合治疗。