Grossi Francesco, Aita Marianna
Medical Oncology A, Disease Management Team, Lung Cancer, National Institute for Cancer Research, Largo Rosanna Benzi, Genova, Italy.
Expert Opin Biol Ther. 2007 Jul;7(7):1107-19. doi: 10.1517/14712598.7.7.1107.
Although platinum-based chemotherapy remains a mainstay of non-small-cell lung cancer treatment, its efficacy has probably reached a plateau. Increased understanding of cancer biology has allowed the identification of a number of possible molecular targets, including the EGF receptor and the angiogenesis pathway. ECOG-E4599 has randomised chemonaive patients to receive paclitaxel--carboplatin with and without bevacizumab, a humanised monoclonal antibody targeting the VEGF. The study is the first to show a survival advantage of adding a biological agent to chemotherapy in this setting: in particular, for the first time the survival of lung cancer patients has been extended beyond 1 year. The aim of this review is to describe the biological and clinical properties of bevacizumab and to discuss the evidence that has supported its approval for the first-line treatment of advanced non-squamous non-small-cell lung cancer.
尽管铂类化疗仍是非小细胞肺癌治疗的主要手段,但其疗效可能已达平台期。对癌症生物学认识的加深使得人们确定了一些可能的分子靶点,包括表皮生长因子受体(EGF受体)和血管生成途径。东部肿瘤协作组(ECOG)开展的E4599研究将初治患者随机分为两组,分别接受含或不含贝伐单抗(一种靶向血管内皮生长因子(VEGF)的人源化单克隆抗体)的紫杉醇-卡铂化疗。该研究首次表明,在此情况下化疗联合生物制剂可带来生存获益:尤其是肺癌患者的生存期首次延长至1年以上。本综述旨在描述贝伐单抗的生物学和临床特性,并讨论支持其被批准用于一线治疗晚期非鳞非小细胞肺癌的证据。