Perez-Soler R
Department of Thoracic/Head and Neck Medical Oncology, The University of Texas M.D. Anderson Cancer Center, Houston 77030, USA.
Semin Oncol. 1997 Dec;24(6 Suppl 20):S20-34-S20-41.
According to the American Cancer Society, 178,100 new cases of lung cancer were predicted in 1997, with an estimated 5-year relative survival rate of 11% to 14%. Non-small cell lung cancer (NSCLC), the most prevalent type of lung cancer, presents an extraordinary challenge to the oncologist, because most patients present with advanced unresectable disease. Cisplatin, one of the most effective single agents against NSCLC, has only moderate antitumor effect and limited impact on survival. Combination regimens also show little increase in survival. In the search for better treatments for NSCLC, new agents with novel mechanisms of action have been explored. In preclinical studies, topotecan (Hycamtin; SmithKline Beecham Pharmaceuticals, Philadelphia, PA), a topoisomerase I inhibitor, demonstrated activity in a variety of animal tumor models. Results from subsequent phase I and phase II clinical trials, summarized here, suggest that topotecan has modest activity against NSCLC and that its role in the treatment of this disease should be evaluated further.
根据美国癌症协会预测,1997年有178,100例新发肺癌病例,估计5年相对生存率为11%至14%。非小细胞肺癌(NSCLC)是最常见的肺癌类型,给肿瘤学家带来了巨大挑战,因为大多数患者就诊时已患有无法切除的晚期疾病。顺铂是治疗NSCLC最有效的单一药物之一,但其抗肿瘤效果一般,对生存率的影响有限。联合治疗方案对生存率的提高也不明显。为了寻找更好的NSCLC治疗方法,人们探索了具有新作用机制的新药物。在临床前研究中,拓扑替康(Hycamtin;史克必成制药公司,宾夕法尼亚州费城),一种拓扑异构酶I抑制剂,在多种动物肿瘤模型中显示出活性。本文总结的后续I期和II期临床试验结果表明,拓扑替康对NSCLC有一定活性,其在该疾病治疗中的作用应进一步评估。