Saijo N
National Cancer Center Hospital, Tsukiji 5-1-1, Chuo-ku, Tokyo 104-0045, Japan.
Ann N Y Acad Sci. 2000;922:92-9. doi: 10.1111/j.1749-6632.2000.tb07028.x.
CPT-11, developed by Yakult Honsha, has achieved the position of standard chemotherapy for colorectal cancer in the United States and in Western countries because CPT-11 + 5FU + LV showed survival benefit compared with 5FU-LV in two randomized controlled trials. CPT-11 has been distributed to almost all countries. In Japan, combination therapy of CDDP + CPT-11 was significantly superior to CDDP-VP-16 in the treatment of extensive disease small cell lung cancer. This combination is also active against non-small cell lung cancer. Daiich Pharmaceutical Co. developed a more active nonmasked form of camptothecin derivative, DX-8915f. The phase I study of a new camptothecin inhibitor, DX-8915f, has just been completed. The new topoisomerase I inhibitors of indolocarbazol derivatives, NB-506 and J107088, developed by Banyu Co., have strong antitumor activity and a wide therapeutic ratio. The phase I trial of J107088 is currently ongoing in the United States and Japan. These do not show any cross-resistance to MDR drugs.
由养乐多公司研发的伊立替康(CPT-11)在美国和西方国家已成为结直肠癌的标准化疗药物,因为在两项随机对照试验中,与氟尿嘧啶-亚叶酸(5FU-LV)相比,伊立替康+5氟尿嘧啶(5FU)+亚叶酸(LV)显示出了生存获益。伊立替康已在几乎所有国家上市。在日本,顺铂(CDDP)+伊立替康(CPT-11)联合疗法在广泛期小细胞肺癌的治疗中显著优于顺铂-依托泊苷(CDDP-VP-16)。这种联合疗法对非小细胞肺癌也有活性。第一制药公司研发了一种活性更高的非掩蔽型喜树碱衍生物DX-8915f。新型喜树碱抑制剂DX-8915f的I期研究刚刚完成。由半谷公司研发的新型吲哚咔唑衍生物拓扑异构酶I抑制剂NB-506和J107088具有很强的抗肿瘤活性和较宽的治疗指数。J107088的I期试验目前正在美国和日本进行。这些药物对多药耐药(MDR)药物没有任何交叉耐药性。