Isobe Takeshi, Herbst Roy S, Onn Amir
Department of Thoracic/Head and Neck Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston, TX 77030, USA.
Semin Oncol. 2005 Jun;32(3):315-28. doi: 10.1053/j.seminoncol.2005.02.016.
Lung cancer is one of the most frequent causes of cancer-related death in the United States. For patients with advanced non-small cell lung cancer (NSCLC), chemotherapy, alone or in combination with radiation therapy, is considered the standard treatment. Although this treatment may result in a modest improvement in patient survival, overall prognosis of these patients remains dismal, and the treatment is nonspecific, nonselective, and toxic. Therefore, new therapeutic strategies are needed. During the past decade, several molecules that contribute to lung cancer progression and metastasis have been identified. Growth factors and proangiogenic factors have been the focus of intense research in cancer since therapeutic approaches for their inhibition do exist. The role of these factors was studied in different organs and tumors and was found to be phenotypically distinct. Several molecular targeted therapies have shown efficacy and had been approved for treatment of specific cancers. Most advanced in clinical research for lung cancer are targeted therapies that inhibit the epidermal growth factor receptor (EGFR) and the vascular endothelial growth factor (VEGF) signaling pathways. Others are signaling pathway inhibitors. The first targeted therapy for lung cancer is gefitinib, an EGFR inhibitor, which was approved in several countries in 2003. Goals of molecular targeted therapy studies include the following: better understanding of the exact role of particular growth factors in specific tumors; establishment of new clinical study designs for biological agents; and tailoring appropriate combinations of conventional chemotherapy and/or radiotherapy with biological therapy for specific patients. Achievement of these goals will hopefully lead to incorporation of biological therapy into the current anticancer arsenal, for the benefit of lung cancer patients.
肺癌是美国癌症相关死亡的最常见原因之一。对于晚期非小细胞肺癌(NSCLC)患者,单独化疗或联合放疗被视为标准治疗方法。尽管这种治疗可能会使患者生存率略有提高,但这些患者的总体预后仍然不佳,而且该治疗是非特异性、非选择性且有毒性的。因此,需要新的治疗策略。在过去十年中,已经鉴定出几种促进肺癌进展和转移的分子。生长因子和促血管生成因子一直是癌症深入研究的重点,因为确实存在针对它们的抑制性治疗方法。这些因子在不同器官和肿瘤中的作用得到了研究,并且发现其表型各不相同。几种分子靶向疗法已显示出疗效,并已被批准用于治疗特定癌症。在肺癌临床研究中进展最为显著的是抑制表皮生长因子受体(EGFR)和血管内皮生长因子(VEGF)信号通路的靶向疗法。其他的是信号通路抑制剂。第一种肺癌靶向疗法是吉非替尼,一种EGFR抑制剂,于2003年在多个国家获得批准。分子靶向治疗研究的目标包括以下几点:更好地了解特定生长因子在特定肿瘤中的确切作用;建立生物制剂的新临床研究设计;以及为特定患者量身定制传统化疗和/或放疗与生物治疗的合适组合。实现这些目标有望将生物治疗纳入当前的抗癌武器库,以造福肺癌患者。