Fritze D, Massner B, Becher R, Kaufmann M, Illiger H J, Hartlapp J, Queisser W, Abel U, Edler L, Mayr A C
Klin Wochenschr. 1984 Feb 15;62(4):162-7. doi: 10.1007/BF01731638.
From January 1978 to December 1980, 222 patients with metastatic breast cancer were included into a prospective multicenter trial. All patients were treated once a month with six cycles of VAC- (vincristine, adriamycin, cyclophosphamide) chemotherapy, followed by FMC (5-fluorouracil, methotrexate, cyclophosphamide) until progression was documented. By random assignment, the patients received immunostimulation with Corynebacterium parvum (CP) by one of four methods: subcutaneous (SC) on either day 1 or day 14, intravenous (IV) on either day 1 or day 14. The 214 evaluable patients were equally distributed to the four arms. The rates of complete or partial response to VAC/FMC plus CP did not differ significantly between the treatment groups. Of our patients, 22-33% were definite treatment failures. The Kaplan-Meier curves of duration of remission (medians 14 vs. 9 vs. 13 vs. 11 months) did not differ significantly. Only small differences in survival were noted among the four study groups (medians 15.4 vs. 17.5 vs. 17.2 vs. 13.0 months). However, complete and partial responders lived significantly longer (Log rank test P = 0.008), when CP was given on day 14 by the SC rather than IV route (29+ vs. 14.3 months). Patients in the four study groups were treated with virtually identical doses of VAC/FMC chemotherapy. Patients receiving CP intravenously on day 14 experienced significantly lower mean leukocyte counts than patients in the other groups. Many patients suffered from high temperature (requiring treatment with antipyretics) and severe gastrointestinal toxicity, particularly when CP was given IV on day 1 together with the chemotherapy.(ABSTRACT TRUNCATED AT 250 WORDS)
1978年1月至1980年12月,222例转移性乳腺癌患者被纳入一项前瞻性多中心试验。所有患者每月接受一次共六个周期的VAC(长春新碱、阿霉素、环磷酰胺)化疗,随后接受FMC(5-氟尿嘧啶、甲氨蝶呤、环磷酰胺)治疗,直至记录到病情进展。通过随机分配,患者采用四种方法之一接受短小棒状杆菌(CP)免疫刺激:第1天或第14天皮下注射(SC),第1天或第14天静脉注射(IV)。214例可评估患者平均分配到四个组。各治疗组对VAC/FMC加CP的完全或部分缓解率无显著差异。我们的患者中,22%-33%为明确的治疗失败病例。缓解期的Kaplan-Meier曲线(中位数分别为14个月、9个月、13个月和11个月)无显著差异。四个研究组之间仅观察到生存方面的微小差异(中位数分别为15.4个月、17.5个月、17.2个月和13.0个月)。然而,当第14天通过皮下而非静脉途径给予CP时,完全和部分缓解者的生存期显著延长(对数秩检验P = 0.008,分别为29 +个月和14.3个月)。四个研究组的患者接受的VAC/FMC化疗剂量基本相同。第14天接受静脉CP治疗的患者平均白细胞计数显著低于其他组患者。许多患者出现高热(需要用退烧药治疗)和严重的胃肠道毒性,尤其是当第1天静脉给予CP并同时进行化疗时。(摘要截取自250字)