Breast Cancer Program, Department of Oncology, Vall d'Hebron University Hospital, Vall d'Hebron 119-129, Barcelona, Spain.
Breast Cancer Res Treat. 2012 Jun;133(3):821-30. doi: 10.1007/s10549-011-1875-6. Epub 2011 Nov 24.
Taxanes are a standard first-line option for metastatic breast cancer (MBC), but their utility may be limited by primary or acquired resistance. New microtubule-targeting agents have been developed to overcome taxane resistance and provide additional options for improving patient outcomes. This article reviews these alternative microtubule-targeting agents and their potential clinical benefits for MBC patients. Relevant clinical data were compiled through searches within PubMed and congress abstract databases. Ixabepilone, a novel microtubule-stabilizing drug approved by the US Food and Drug Administration (FDA), has proven efficacy across multiple lines of therapy, including patients with taxane-resistant/refractory disease. In phase III trials, ixabepilone plus capecitabine significantly improved progression-free survival compared with capecitabine alone in anthracycline/taxane-pretreated patients. Eribulin has recently been approved by the FDA and by the European Medicines Agency for the treatment of patients with MBC who have received at least two prior chemotherapy regimens for late-stage disease. In a phase III trial, eribulin extended overall survival compared with the physician's treatment choice in heavily pretreated MBC patients. In addition, several investigational microtubule-targeting agents may have therapeutic potential in MBC. The development of new microtubule-targeting agents helps to address the need for additional effective regimens for patients progressing after standard treatment with anthracycline- and taxane-containing regimens.
紫杉烷类药物是转移性乳腺癌(MBC)的标准一线治疗选择,但由于原发性或获得性耐药,其应用可能受到限制。已经开发了新的微管靶向药物来克服紫杉烷类耐药性,并为改善患者预后提供更多选择。本文综述了这些替代微管靶向药物及其对 MBC 患者的潜在临床获益。通过在 PubMed 和会议摘要数据库中进行搜索,汇编了相关的临床数据。伊沙匹隆是一种新型微管稳定剂药物,已被美国食品和药物管理局(FDA)批准用于治疗多种治疗线的疾病,包括紫杉烷类耐药/难治性疾病患者。在 III 期临床试验中,与卡培他滨单药治疗相比,伊沙匹隆联合卡培他滨显著改善了蒽环类/紫杉烷类预处理患者的无进展生存期。艾日布林最近已被 FDA 和欧洲药品管理局批准用于治疗至少接受过两种晚期疾病化疗方案的 MBC 患者。在 III 期临床试验中,与医生选择的治疗方案相比,艾日布林延长了晚期 MBC 患者的总生存期。此外,几种研究中的微管靶向药物在 MBC 中可能具有治疗潜力。新的微管靶向药物的开发有助于满足在标准蒽环类和紫杉烷类方案治疗后进展的患者对其他有效方案的需求。