Winter M C, Holen I, Coleman R E
Academic Unit of Clinical Oncology, Section for Cancer, Cancer Research Centre, University of Sheffield, Weston Park Hospital, Sheffield S10 2SJ, UK.
Cancer Treat Rev. 2008 Aug;34(5):453-75. doi: 10.1016/j.ctrv.2008.02.004.
Bisphosphonates are potent inhibitors of osteoclast-mediated bone resorption and are firmly established in the management of breast cancer patients with metastatic skeletal disease. There are extensive data that bisphosphonates, particularly nitrogen-containing bisphosphonates such as zoledronic acid, exhibit anti-tumour activity potentially via both indirect and direct mechanisms in vitro. In vivo studies using animal models of breast cancer induced bone disease have shown that bisphosphonates exert anti-tumour effects via inhibiting osteolysis and reducing skeletal tumour burden. Furthermore, pre-clinical studies have demonstrated synergistic anti-tumour effects between chemotherapy agents commonly used in breast cancer treatment and nitrogen-containing bisphosphonates. This, coupled with emerging evidence from pre-clinical in vivo studies suggesting that bisphosphonates may have additional anti-tumour activity outside of the bone microenvironment, could be of significant importance in the clinical management of breast cancer. The evidence in favour of an anti-tumour effect of bisphosphonates in the clinical setting is inconclusive however, with conflicting evidence from several trials. This review focuses on the anti-tumour activity of bisphosphonates in breast cancer, with particular focus on zoledronic acid. The pre-clinical evidence for anti-tumour activity will be reviewed, followed by the synergistic effects with anti-cancer agents. Finally, the clinical relevance and strategies for the evaluation of anti-tumour activity in breast cancer will be discussed. We are currently exploring the potential synergistic anti-tumour effects of the sequential treatment of neoadjuvant chemotherapy followed by zoledronic acid in a randomised phase II study evaluating biological endpoints including apoptosis, proliferation and angiogenesis in patients with breast cancer.
双膦酸盐是破骨细胞介导的骨吸收的强效抑制剂,在转移性骨骼疾病的乳腺癌患者管理中已得到广泛应用。有大量数据表明,双膦酸盐,特别是含氮双膦酸盐如唑来膦酸,在体外可能通过间接和直接机制表现出抗肿瘤活性。使用乳腺癌诱导性骨病动物模型的体内研究表明,双膦酸盐通过抑制骨溶解和减轻骨骼肿瘤负担发挥抗肿瘤作用。此外,临床前研究已证明乳腺癌治疗中常用的化疗药物与含氮双膦酸盐之间具有协同抗肿瘤作用。这一点,再加上临床前体内研究的新证据表明双膦酸盐可能在骨微环境之外具有额外的抗肿瘤活性,可能对乳腺癌的临床管理具有重要意义。然而,支持双膦酸盐在临床环境中具有抗肿瘤作用的证据并不确凿,几项试验的证据相互矛盾。本综述重点关注双膦酸盐在乳腺癌中的抗肿瘤活性,尤其关注唑来膦酸。将回顾抗肿瘤活性的临床前证据,随后讨论其与抗癌药物的协同作用。最后,将讨论乳腺癌中抗肿瘤活性评估的临床相关性及策略。我们目前正在一项随机II期研究中探索新辅助化疗序贯唑来膦酸的潜在协同抗肿瘤作用,该研究评估乳腺癌患者的生物学终点,包括细胞凋亡、增殖和血管生成。