Falandry C, Canney P A, Freyer G, Dirix L Y
Department of Medical Oncology, Centre Hospitalier Lyon Sud, Pierre-Bénite, France.
Ann Oncol. 2009 Apr;20(4):615-20. doi: 10.1093/annonc/mdn693. Epub 2009 Mar 2.
Aromatase inhibitors (AIs) are well established in the treatment of metastatic hormone-sensitive breast cancer in postmenopausal women. Cyclooxygenase (COX)-2 inhibitors have demonstrated efficacy in reducing cancer risk in animal and human studies. In several preclinical studies, combination AI plus COX-2 inhibitor therapy has shown a synergistic antitumor effect. This review describes the utility of AI plus COX-2 inhibitor therapy and discusses the completed and ongoing clinical trials investigating treatment with the AI exemestane and the COX-2 inhibitor celecoxib in the neo-adjuvant and metastatic breast cancer settings. In general, combination therapy had comparable or better efficacy compared with AI monotherapy using the end points of progression-free survival, overall response rate, clinical benefit rate, time to progression, and duration of clinical benefit. All therapies were well tolerated. There appeared to be a beneficial impact on serum lipid levels for patients receiving combination therapy in a neo-adjuvant trial despite the known cardiovascular toxicity risk associated with COX-2 inhibitors. In conclusion, AIs plus COX-2 inhibitors have shown promising efficacy and safety for the treatment of patients with metastatic breast cancer. Careful monitoring during future trials will be necessary to accurately assess the risk-benefit ratio of combination therapy.
芳香化酶抑制剂(AIs)在绝经后女性转移性激素敏感性乳腺癌的治疗中已得到充分确立。环氧化酶(COX)-2抑制剂在动物和人体研究中已证明具有降低癌症风险的功效。在多项临床前研究中,AI联合COX-2抑制剂治疗已显示出协同抗肿瘤作用。本综述描述了AI联合COX-2抑制剂治疗的效用,并讨论了正在进行和已完成的临床试验,这些试验研究了在新辅助和转移性乳腺癌背景下使用AI依西美坦和COX-2抑制剂塞来昔布进行治疗的情况。总体而言,与使用无进展生存期、总缓解率、临床受益率、进展时间和临床受益持续时间等终点的AI单药治疗相比,联合治疗具有相当或更好的疗效。所有治疗耐受性良好。尽管已知COX-2抑制剂存在心血管毒性风险,但在一项新辅助试验中,接受联合治疗的患者的血脂水平似乎受到有益影响。总之,AI联合COX-2抑制剂在治疗转移性乳腺癌患者方面已显示出有前景的疗效和安全性。在未来试验期间进行仔细监测对于准确评估联合治疗的风险效益比将是必要的。