Shinkai T, Saijo N, Tominaga K, Eguchi K, Shimizu E, Sasaki Y, Fujita J, Futami H
Cancer Treat Rep. 1985 Sep;69(9):945-51.
Fifty-eight patients with advanced non-small cell lung cancer were randomly allocated to receive vindesine (3 mg/m2 every week) plus either cisplatin (80 mg/m2 every 3 weeks) or mitomycin (8 mg/m2 weekly X 3, then every 3 weeks). No patients achieved complete response. Among the 28 patients treated with vindesine plus cisplatin, there were 12 partial responders (42.9%); among the 30 patients treated with vindesine plus mitomycin, there were only three partial responders (10%) (P less than 0.005). The median duration of response was 11.5 weeks (range, 4-25) in the patients treated with vindesine plus cisplatin. The median survival times for patients treated with vindesine plus cisplatin and vindesine plus mitomycin were 10.1 and 10.2 months, respectively; there was no statistical difference in survival time between the two groups. Initial performance status was the strong predictor of patient survival. Toxic effects, including moderate myelosuppression, nephrotoxicity, peripheral neuropathy, and gastrointestinal symptoms, were generally manageable. The combination of vindesine and cisplatin appears to be effective against advanced non-small cell lung cancer.
58例晚期非小细胞肺癌患者被随机分配接受长春地辛(每周3mg/m²)联合顺铂(每3周80mg/m²)或丝裂霉素(每周8mg/m²,共3周,然后每3周一次)治疗。无患者达到完全缓解。在接受长春地辛联合顺铂治疗的28例患者中,有12例部分缓解者(42.9%);在接受长春地辛联合丝裂霉素治疗的30例患者中,仅有3例部分缓解者(10%)(P<0.005)。接受长春地辛联合顺铂治疗的患者的中位缓解持续时间为11.5周(范围4 - 25周)。接受长春地辛联合顺铂和长春地辛联合丝裂霉素治疗的患者的中位生存时间分别为10.1个月和10.2个月;两组生存时间无统计学差异。初始体能状态是患者生存的强预测因素。包括中度骨髓抑制、肾毒性、周围神经病变和胃肠道症状在内的毒性反应一般可控制。长春地辛与顺铂联合应用似乎对晚期非小细胞肺癌有效。