Escudier Bernard, Cosaert Jan, Pisa Pavel
Immunotherapy Unit, Institut Gustave Roussy, Villejuif Cedex, France.
Expert Rev Anticancer Ther. 2008 Oct;8(10):1545-57. doi: 10.1586/14737140.8.10.1545.
Bevacizumab, in combination with IFN, is approved in the EU as first-line therapy for advanced and/or metastatic renal cell carcinoma (mRCC). Data from Avastin and Roferon in Renal Cell Carcinoma [BO17705] (AVOREN), a Phase III trial, demonstrated that bevacizumab plus IFN significantly improves progression-free survival and response rate in patients with previously untreated mRCC compared with IFN plus placebo. Furthermore, bevacizumab plus IFN is well tolerated and has a predictable and well-established tolerability profile; reducing the dose of IFN, when necessary, can effectively manage IFN-related side effects without compromising efficacy. The rapid evolution of options for RCC therapy means that the optimal use of available agents to maximize patient benefit is not currently well defined. Combination regimens and sequencing of agents are both being investigated to maximize future outcomes, with bevacizumab playing a key role in first-line regimens. Trials over the next 5 years will guide clinical practice, but bevacizumab plus IFN is currently a standard first-line option for mRCC.
贝伐单抗联合干扰素在欧盟被批准作为晚期和/或转移性肾细胞癌(mRCC)的一线治疗方案。一项III期试验“肾细胞癌中的阿瓦斯汀和罗扰素[BO17705](AVOREN)”的数据表明,与干扰素加安慰剂相比,贝伐单抗加干扰素可显著提高既往未治疗的mRCC患者的无进展生存期和缓解率。此外,贝伐单抗加干扰素耐受性良好,具有可预测且已确立的耐受性特征;必要时减少干扰素剂量可有效管理与干扰素相关的副作用,而不影响疗效。肾细胞癌治疗方案的快速演变意味着目前尚未明确如何最佳使用现有药物以使患者受益最大化。正在研究联合治疗方案和药物的序贯使用,以实现最佳未来疗效,贝伐单抗在一线治疗方案中发挥关键作用。未来5年的试验将指导临床实践,但贝伐单抗加干扰素目前是mRCC的标准一线治疗选择。