Colleoni M, Nelli P, Gaion F, Sgarbossa G, Manente P
Service of Medical Oncology, City Hospital, Castelfranco Veneto, Italy.
Oncology. 1995 Nov-Dec;52(6):435-8. doi: 10.1159/000227506.
The combination chemotherapy including mitoxantrone, fluorouracil and leucovorin has proven to be effective and well-tolerated in advanced breast cancer (ABC). No data are available on the association with navelbine, a new vinka alkaloid, which has demonstrated high activity in ABC. The trial was designed to evaluate feasibility and efficacy of the association of vinorelbine to mitoxantrone, fluorouracil and L-leucovorin in patients who failed a previous regimen for ABC or who relapsed within 6 months of adjuvant chemotherapy. The schedule was as follows: mitoxantrone 6 mg/m2 days 1 and 8; L-leucovorin 250 mg/m2 days 1 and 8, fluorouracil 600 mg/m2 days 1 and 8, vinorelbine 25 mg/m2 days 1 and 8, cycles being repeated every 21 days. Twenty-five patients were enrolled and are evaluable for response and side effects. One hundred cycles of therapy have been delivered (median/patient, 4 cycles). In 41 cycles a delay was required and in 38 cycles it was necessary to administer granulocyte colony-stimulating factor for neutropenia. Seven partial remissions (28%; 95% confidence interval, 12-49%), 10 stabilizations of disease and 8 progressions were observed. Although grade 4 neutropenia was observed in 44% of the patients, no grade 3-4 infections were observed. Nonhematologic toxicities were mild or moderate and included alopecia, mucositis and phlebitis. In conclusion, the schedule employed, although correlated with a moderate activity, does not seem to be superior to other regimens with mitoxantrone, fluorouracil, and leucovorin.
包括米托蒽醌、氟尿嘧啶和亚叶酸钙的联合化疗已被证明在晚期乳腺癌(ABC)中有效且耐受性良好。关于与一种新的长春花生物碱诺维本联合使用的数据尚无报道,该生物碱在ABC中已显示出高活性。该试验旨在评估诺维本与米托蒽醌、氟尿嘧啶和L-亚叶酸钙联合使用在先前ABC治疗方案失败或辅助化疗后6个月内复发的患者中的可行性和疗效。治疗方案如下:米托蒽醌6mg/m²,第1天和第8天;L-亚叶酸钙250mg/m²,第1天和第8天,氟尿嘧啶600mg/m²,第1天和第8天,诺维本25mg/m²,第1天和第8天,每21天重复一个周期。25名患者入组并可评估疗效和副作用。已进行了100个周期的治疗(中位/患者,4个周期)。在41个周期中需要延迟治疗,在38个周期中因中性粒细胞减少需要给予粒细胞集落刺激因子。观察到7例部分缓解(28%;95%置信区间,12-49%),10例病情稳定和8例进展。虽然44%的患者出现4级中性粒细胞减少,但未观察到3-4级感染。非血液学毒性为轻度或中度,包括脱发、粘膜炎和静脉炎。总之,所采用的方案虽然有一定活性,但似乎并不优于其他含米托蒽醌、氟尿嘧啶和亚叶酸钙的方案。