Dy Grace K, Adjei Alex A
Department of Medicine, Mayo Clinic, Rochester, MN 55905, USA.
J Clin Oncol. 2002 Jul 1;20(13):3016-28. doi: 10.1200/JCO.2002.02.112.
Lung cancer is the second most common form of cancer in the United States, and although it accounts for 15% of all cancers, it is the most lethal, accounting for approximately 28% of cancer deaths. In 2002, it is estimated that 177,000 new cases of lung cancer will be diagnosed in the United States, and an estimated 160,000 men and women will die from the disease. This mortality rate is greater than that attributable to colorectal, breast, and prostate cancer combined. Systemic treatments for lung cancer with standard chemotherapy agents are still relatively ineffective. Agents targeting novel proliferative and survival pathways in lung cancer are needed to improve treatment outcomes. In recent years, numerous agents inhibiting aberrant processes in tumor cells have undergone clinical evaluation. This review is the second of a two-part series that summarizes pertinent preclinical and clinical information on novel drugs that target critical abnormalities in lung cancer. In this article, agents that were developed to inhibit various aspects of tumor protein trafficking and protein degradation, cell cycle regulation, angiogenesis, and antigenicity are described. Future approaches to treatment are suggested.
肺癌是美国第二常见的癌症形式,尽管它占所有癌症的15%,却是最致命的,约占癌症死亡人数的28%。据估计,2002年美国将有17.7万例新发肺癌病例被诊断出来,预计将有16万男性和女性死于该病。这一死亡率高于结直肠癌、乳腺癌和前列腺癌三者死亡率之和。使用标准化疗药物对肺癌进行全身治疗仍然相对无效。需要针对肺癌中新型增殖和生存途径的药物来改善治疗效果。近年来,许多抑制肿瘤细胞异常过程的药物都进行了临床评估。本综述是一个两部分系列的第二篇,总结了针对肺癌关键异常的新型药物的相关临床前和临床信息。在本文中,描述了为抑制肿瘤蛋白运输和蛋白降解、细胞周期调控、血管生成和抗原性等各个方面而开发的药物。并提出了未来的治疗方法。