Adis, a Wolters Kluwer Business, Mairangi Bay, North Shore, Auckland, New Zealand.
Drugs. 2010 Oct 22;70(15):1987-2010. doi: 10.2165/11205010-000000000-00000.
Cetuximab (Erbitux®) is a chimeric monoclonal antibody directed against the human epidermal growth factor receptor (EGFR). EGFR is overexpressed and/or upregulated in most squamous cell carcinomas of the head and neck (SCCHN); this overexpression is associated with more aggressive disease and poorer prognosis. In the EU, cetuximab is approved in combination with radiation therapy for the treatment of locally advanced SCCHN and in combination with platinum-based chemotherapy for the treatment of recurrent and/or metastatic SCCHN. In randomized, open-label, multinational, phase III clinical trials, cetuximab plus radiotherapy significantly improved the duration of locoregional control (primary endpoint) compared with radiotherapy alone in patients with locally advanced SCCHN, while cetuximab plus first-line platinum-based chemotherapy significantly improved overall survival (primary endpoint) compared with first-line platinum-based chemotherapy alone in patients with recurrent and/or metastatic SCCHN. The efficacy benefits of cetuximab-based combination therapy were achieved without an adverse impact on patients' health-related quality of life. In addition, cetuximab had an acceptable tolerability profile when added to radiotherapy or platinum-based chemotherapy; in particular, it did not exacerbate the toxicities commonly associated with these other treatment modalities. Cetuximab-related adverse events, which include skin rash, hypomagnesaemia and infusion-related reactions, are mostly mild to moderate in severity and manageable. Thus, cetuximab-based combination therapy is a valuable treatment option in patients with SCCHN. In the setting of locally advanced, unresectable disease, cetuximab plus radiotherapy offers an alternative approach to the current standard of care, namely platinum-based chemotherapy plus radiotherapy (chemoradiotherapy). Based on informal comparisons, cetuximab plus radiotherapy appears to be at least as effective as chemoradiotherapy and, moreover, less toxic; however, formal comparisons of these regimens are required before their relative efficacy and tolerability can be conclusively determined. In the setting of recurrent and/or metastatic SCCHN, cetuximab plus platinum-based chemotherapy provides a first-line treatment of choice for fit patients in whom palliative chemotherapy is indicated.
西妥昔单抗(Erbitux®)是一种针对人表皮生长因子受体(EGFR)的嵌合单克隆抗体。EGFR 在头颈部鳞状细胞癌(SCCHN)中过度表达和/或上调;这种过度表达与更具侵袭性的疾病和更差的预后相关。在欧盟,西妥昔单抗被批准与放疗联合用于治疗局部晚期 SCCHN,与铂类化疗联合用于治疗复发性和/或转移性 SCCHN。在随机、开放标签、多中心、III 期临床试验中,与单独放疗相比,西妥昔单抗联合放疗显著改善了局部区域控制的持续时间(主要终点),在复发性和/或转移性 SCCHN 患者中,西妥昔单抗联合一线铂类化疗显著改善了总生存期(主要终点)。与单独使用一线铂类化疗相比,西妥昔单抗联合治疗的疗效获益并未对患者的健康相关生活质量产生不利影响。此外,西妥昔单抗与放疗或铂类化疗联合使用时具有可接受的耐受性;特别是,它没有加剧这些其他治疗方式常见的毒性。西妥昔单抗相关不良反应包括皮疹、低镁血症和输注相关反应,大多为轻至中度,且可控制。因此,西妥昔单抗联合治疗是 SCCHN 患者的一种有价值的治疗选择。在局部晚期、不可切除疾病的情况下,西妥昔单抗联合放疗为当前的标准治疗方法,即铂类化疗联合放疗(放化疗)提供了一种替代方法。基于非正式比较,西妥昔单抗联合放疗似乎至少与放化疗一样有效,而且毒性更小;然而,在确定这些方案的相对疗效和耐受性之前,需要对这些方案进行正式比较。在复发性和/或转移性 SCCHN 的情况下,对于适合接受姑息性化疗的患者,西妥昔单抗联合铂类化疗是一线治疗选择。