Yoshimoto J, Ochi J, Tanahashi T, Nanba K, Saegusa M, Hara M, Akagi T, Obama T, Tsushima T, Ozaki Y
Gan To Kagaku Ryoho. 1987 Feb;14(2):434-9.
Eleven patients with advanced adenocarcinoma of the prostate were treated with a cyclic alternating chemotherapy (VIP-DMF therapy), consisting of a three-drug combination of vincristine, ifosfamide, and peplomycin; and a three-drug combination of adriamycin, mitomycin C and 5-fluorouracil. Each cycle was repeated every 3 or 4 weeks. Of these patients, 9 were refractory to prior hormonal therapy and 8 (89%) achieved an objective response (3 partial, 6 stable) using the criteria of the U.S. National Prostatic Cancer Project. In the patients showing objective response, the duration was from 3 to 18 months with a median duration of 6 months. The survival periods from the initiation of chemotherapy in effective cases ranged from 6 to 20+ months with a median duration of 11 months. The major toxicity was myelosuppression, although no patients suffered life-threatening toxicity. We consider that VIP-DMF therapy is a useful regimen for the treatment of advanced prostatic cancer.
11例晚期前列腺腺癌患者接受了一种周期性交替化疗(VIP-DMF疗法),该疗法由长春新碱、异环磷酰胺和培洛霉素的三药联合方案,以及阿霉素、丝裂霉素C和5-氟尿嘧啶的三药联合方案组成。每个周期每3或4周重复一次。在这些患者中,9例对先前的激素治疗无效,按照美国国家前列腺癌项目的标准,8例(89%)获得了客观缓解(3例部分缓解,6例病情稳定)。在显示出客观缓解的患者中,缓解持续时间为3至18个月,中位持续时间为6个月。有效病例中化疗开始后的生存期为6至20多个月,中位持续时间为11个月。主要毒性为骨髓抑制,尽管没有患者出现危及生命的毒性。我们认为VIP-DMF疗法是治疗晚期前列腺癌的一种有效方案。