Swisher S G, Roth J A
Department of Thoracic and Cardiovascular Surgery, The University of Texas MD Anderson Cancer Center, Box 109, Houston, TX 77030, USA.
Curr Oncol Rep. 2000 Jan;2(1):64-70. doi: 10.1007/s11912-000-0012-1.
The poor overall survival rates associated with non- small-cell lung cancer despite advances in chemotherapy, radiotherapy, and surgery mandate the search for novel approaches. Advances in gene transfer technology have allowed gene therapy strategies to develop that act in such a way as to stimulate the immune system, transfer "suicide" genes, inactivate oncogenes, replace tumor suppressor genes, and transfer pro-apoptotic genes. Clinical trials evaluating these possibilities have begun, and findings indicate that the transfer of tumor sup- pressor genes (wild-type p53) is feasible and has low overall toxicity. Subsequent clinical trials have begun to evaluate the clinical potential of these approaches in non-small-cell lung cancer.
尽管在化疗、放疗和手术方面取得了进展,但非小细胞肺癌的总体生存率仍然很低,这就需要寻找新的治疗方法。基因转移技术的进步使得基因治疗策略得以发展,这些策略可以通过刺激免疫系统、转移“自杀”基因、使癌基因失活、替代肿瘤抑制基因以及转移促凋亡基因等方式发挥作用。评估这些可能性的临床试验已经开始,结果表明肿瘤抑制基因(野生型p53)的转移是可行的,且总体毒性较低。随后的临床试验已开始评估这些方法在非小细胞肺癌中的临床潜力。