Ito Y, Hoshino A, Ohara K, Kamiya O, Nagata K, Kojima T, Kinoshita T, Sugiura I
Gan To Kagaku Ryoho. 1985 Oct;12(10):1999-2003.
The effects of combination chemotherapy including mitoxantrone (MXN) "M-VEMFH" for advanced breast cancer were studied. The M-VEMFH regimen consisted of MXN 7 mg/m2, VCR 0.7 mg/m2, EX 333 mg/m2, MTX 13.3 mg/m2 i.v. on day 1, 5-FU 333 mg/m2 i.v. from day 1 to day 5 and pred. (H) 60 mg/m2 p.o. with tapering off in 2 weeks. In 7 cases heavily pretreated with combination chemotherapy including ADR, CR 2, PR 2, NC 2 and PD 1 were observed (response rate 57.1%). In 5 cases without prior ADR, PR 1, NC 2 and PD 2 were obtained. One case given 586 mg/m2 of prior ADR died of congestive heart failure after administration of 47 mg/m2 of NXN. One case died of sepsis. The other side effects were stomatitis, vulvitis, abnormal gustation, nausea, vomiting and alopecia. M-VEMFH is effective combination chemotherapy for advanced breast cancer resistant to ADR, but care must be exerted due to the accompanying cardiotoxicity and leukopenia.
研究了包括米托蒽醌(MXN)的“M-VEMFH”联合化疗方案对晚期乳腺癌的疗效。M-VEMFH方案包括第1天静脉注射米托蒽醌7mg/m²、长春新碱0.7mg/m²、表柔比星333mg/m²、甲氨蝶呤13.3mg/m²,第1天至第5天静脉注射氟尿嘧啶333mg/m²,口服泼尼松(H)60mg/m²,2周内逐渐减量。在7例接受过包括阿霉素在内的联合化疗的重度预处理患者中,观察到完全缓解(CR)2例、部分缓解(PR)2例、疾病稳定(NC)2例和疾病进展(PD)1例(缓解率57.1%)。在5例未接受过阿霉素治疗的患者中,获得部分缓解1例、疾病稳定2例和疾病进展2例。1例之前接受过586mg/m²阿霉素治疗的患者在给予47mg/m²米托蒽醌后死于充血性心力衰竭。1例死于败血症。其他副作用包括口腔炎、外阴炎、味觉异常、恶心、呕吐和脱发。M-VEMFH是对阿霉素耐药的晚期乳腺癌有效的联合化疗方案,但由于伴随的心脏毒性和白细胞减少,必须谨慎使用。