Samonigg H, Stöger H, Kasparek A K, Schmid M, Dusleag J, Pfeiffer K, Smola M, Steindorfer P, Lechner P
Department of Internal Medicine, Karl Franzens-University, Graz, Austria.
Cancer Chemother Pharmacol. 1991;27(6):477-80. doi: 10.1007/BF00685163.
A total of 60 patients with advanced breast cancer were treated with a combination of prednimustine (P: 110 mg/m2, days 1-5), mitoxantrone (M: 12 mg/m2, day 1) and 5-fluorouracil (F: 500 mg/m2, day 1) (PMF). Treatment was repeated every 3 weeks. In all 53 patients were evaluable for response. A total of 12 subjects had failed prior chemotherapy for metastatic disease. In response to PMF treatment we observed 21 partial remissions and 3 complete remissions, amounting to a total response rate of 45%. The median duration of response was 39 weeks, and median survival was 56 weeks. Dose-limiting side effects were leukopenia (40 cases) and thrombocytopenia (11 patients). Nausea and vomiting was experienced by 93% of subjects; in 56% of cases it reached WHO stage II-III. Alopecia occurred in 18% of our patients. Our results suggest that PMF represents an active regimen in the treatment of advanced breast cancer and yields a response rate of 45%. Considering that the majority of our patients had not received prior chemotherapy, the question remains open as to whether a 45% response rate outweighs the observed toxicity.
共有60例晚期乳腺癌患者接受了泼尼松氮芥(P:110mg/m²,第1 - 5天)、米托蒽醌(M:12mg/m²,第1天)和5-氟尿嘧啶(F:500mg/m²,第1天)联合方案(PMF)治疗。每3周重复治疗。所有53例患者可评估疗效。共有12例患者先前针对转移性疾病的化疗失败。针对PMF治疗,我们观察到21例部分缓解和3例完全缓解,总缓解率达45%。缓解的中位持续时间为39周,中位生存期为56周。剂量限制性副作用为白细胞减少(40例)和血小板减少(11例)。93%的患者出现恶心和呕吐;56%的病例达到世界卫生组织II - III级。18%的患者发生脱发。我们的结果表明,PMF是治疗晚期乳腺癌的一种有效方案,缓解率为45%。鉴于我们的大多数患者此前未接受过化疗,45%的缓解率是否超过所观察到的毒性这一问题仍未解决。