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贝伐单抗与非小细胞肺癌:饿死敌人以求生存

Bevacizumab and non-small-cell lung cancer: starving the enemy to survive.

作者信息

Grossi Francesco, Aita Marianna

机构信息

Medical Oncology A, Disease Management Team, Lung Cancer, National Institute for Cancer Research, Largo Rosanna Benzi, Genova, Italy.

出版信息

Expert Opin Biol Ther. 2007 Jul;7(7):1107-19. doi: 10.1517/14712598.7.7.1107.

Abstract

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.

摘要

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。

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