贝伐珠单抗联合紫杉烷类药物用于转移性乳腺癌的一线治疗。

Bevacizumab in combination with taxanes for the first-line treatment of metastatic breast cancer.

机构信息

Medical Oncology, Mount Hospital, Perth, Western Australia, Australia.

Medical Oncology, Mount Vernon Cancer Centre, Middlesex, UK.

出版信息

Ann Oncol. 2010 Dec;21(12):2305-2315. doi: 10.1093/annonc/mdq122. Epub 2010 Mar 24.

Abstract

BACKGROUND

Taxanes are an established treatment of metastatic breast cancer (mBC). Biological therapies that can be effectively combined with taxanes may provide an alternative to taxane-chemotherapy doublets, which are not suitable for all patients.

PATIENTS AND METHODS

Bevacizumab is a humanised mAb against vascular endothelial growth factor (VEGF) which inhibits angiogenesis. This review summarises outcomes from trials evaluating bevacizumab in the first-line treatment of mBC.

RESULTS

Bevacizumab demonstrated considerable efficacy in combination with taxane therapy in the first-line treatment of human epidermal growth factor receptor-2 (HER2)-negative mBC in three phase III trials. Improved response rate and progression-free survival (PFS) were also observed in patients who had received taxanes in the adjuvant setting. Bevacizumab-taxane combinations are effective across a broad range of patient subgroups and have greater efficacy than single-agent taxanes in first-line mBC. Importantly, the tolerability of bevacizumab-taxane combinations compares favourably with that of taxanes in combination with other chemotherapy agents.

CONCLUSIONS

Bevacizumab-taxane combinations provide an alternative to chemotherapy doublet regimens in first-line mBC, with equivalent efficacy and potentially lower toxicity. Ongoing trials are investigating the efficacy and safety of bevacizumab in various stages of breast cancer and in breast cancer with a range of hormonal or receptor characteristics.

摘要

背景

紫杉烷类药物是转移性乳腺癌(mBC)的既定治疗方法。可以与紫杉烷类药物有效联合使用的生物疗法可能为不适合所有患者的紫杉烷类化疗双联疗法提供替代方案。

患者和方法

贝伐珠单抗是人源化单克隆抗体,针对血管内皮生长因子(VEGF),可抑制血管生成。本综述总结了评估贝伐珠单抗在 mBC 一线治疗中的试验结果。

结果

在三项 III 期临床试验中,贝伐珠单抗与紫杉烷类药物联合应用于人表皮生长因子受体-2(HER2)阴性 mBC 的一线治疗中具有显著疗效。在辅助治疗中接受紫杉烷类药物治疗的患者,其缓解率和无进展生存期(PFS)也有所提高。贝伐珠单抗-紫杉烷类药物联合应用在广泛的患者亚组中均有效,并且在一线 mBC 中的疗效优于单药紫杉烷类药物。重要的是,贝伐珠单抗-紫杉烷类药物联合治疗的耐受性与紫杉烷类药物联合其他化疗药物的耐受性相当。

结论

贝伐珠单抗-紫杉烷类药物联合治疗为一线 mBC 中的化疗双联方案提供了替代方案,具有等效的疗效和潜在更低的毒性。正在进行的试验正在研究贝伐珠单抗在乳腺癌各个阶段以及具有各种激素或受体特征的乳腺癌中的疗效和安全性。

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