Bourgeois H, Turpin F, Bouchada M, Volters A, Cvitkovic F, Goupil A, Janvier M, Tubiana-Hulin M, Soulie P, Berlie J, Girard M, Rouesse J
Bull Cancer. 1998 Sep;85(9):794.
Fourty-six patients (41 evaluable) were treated in second line chemotherapy of metastatic breast cancer (MBC) by an association of mitomycin (M), vinorelbine (V) (M 8 mg/m2 D1, V 25 mg/m2 D1 and DI 8 every 4 weeks). Median age was 58 years (36-78), median performance status 1 (0-3). Thirty-seven per cent of the tumors were estrogen receptors positive and 17% progesterone receptors positive.eventeen patients received an adjuvant chemotherapy and 39 a first line chemotherapy with anthracyclin (A). The median number of metastatic sites was 2 (1-4) and 27 patients (67%) had visceral metastases. Twelve patients were refractory to anthracyclins and 5 resistant. No toxic death nor hemolytic uremic syndrom were observed.even (3,7%) febrile neutropenias happened responsible for 4 hospitalizations. A grade 3 or 4 neutropenia was noted in 34% of the cycles but no other clinic toxicity nor grade 3 or 4 thrombopenia. The rate of objective response (OR) was 37,5% with 2 complete responses (CR) and 13 partial responses (PR).even patients had stable disease and 18 progressed. The rate of hepatic OR was 31%. Five (40%) A-refractory patients responded but no resistant patient. Median OR time was 10 weeks (8-12) and median OR duration was 5 months (3-6). Median survival was 11,5 months. MV association is well tolerated and effective in second line chemotherapy for MBC even with hepatic metastasis and in patients refractory to anthracyclins.
46例患者(41例可评估)接受了转移性乳腺癌(MBC)的二线化疗,采用丝裂霉素(M)、长春瑞滨(V)联合方案(M 8mg/m²,第1天;V 25mg/m²,第1天,每4周重复)。中位年龄58岁(36 - 78岁),中位体能状态为1(0 - 3)。37%的肿瘤雌激素受体阳性,17%孕激素受体阳性。17例患者接受过辅助化疗,39例接受过一线蒽环类药物(A)化疗。转移部位的中位数为2个(1 - 4个),27例患者(67%)有内脏转移。12例患者对蒽环类药物难治,5例耐药。未观察到毒性死亡或溶血尿毒综合征。发生3例(7%)发热性中性粒细胞减少症,导致4次住院。34%的化疗周期出现3或4级中性粒细胞减少,但未出现其他临床毒性或3或4级血小板减少。客观缓解率(OR)为37.5%,包括2例完全缓解(CR)和13例部分缓解(PR)。10例患者病情稳定,18例进展。肝脏OR率为31%。5例(40%)对A难治的患者有反应,但耐药患者无反应。中位OR时间为10周(8 - 12周),中位OR持续时间为5个月(3 - 6个月)。中位生存期为11.5个月。MV联合方案耐受性良好,在MBC二线化疗中有效,即使存在肝转移以及对蒽环类药物难治的患者。