De Placido S, Perrone F, Carlomagno C, Morabito A, Pagliarulo C, Lauria R, Marinelli A, De Laurentiis M, Varriale E, Petrella G
Division of Medical Oncology, School of Medicine, University of Naples Federico II, Italy.
Br J Cancer. 1995 Jun;71(6):1283-7. doi: 10.1038/bjc.1995.248.
The aim of this study was to test the hypothesis of Goldie and Coldman that the use of non-cross-resistant regimens of chemotherapy could lead to maximal anti-tumour effect. We compared standard CMF (cyclophosphamide, methotrexate, fluorouracil) with alternating CMF/EV (epirubicin, vincristine) in the adjuvant therapy of early breast cancer. Stage II premenopausal node-positive or post-menopausal node-positive oestrogen receptor-negative and stage III breast cancer patients were eligible for the study. From January 1985 to December 1990, 220 patients were randomised (115 to CMF and 105 to CMF/EV). Toxicity was mild; neurotoxicity, vomiting and hair loss were more frequent in the CMF/EV group, while permanent amenorrhoea, diarrhoea, stomach ache and minor infections occurred more often in the CMF arm. At a follow-up of 48 months, 113 patients (51.4%) had had recurrence (62 on CMF and 51 on CMF/EV) and 54 (24.5%) had died (30 on CMF and 24 on CMF/EV). There was no significant difference in disease-free and overall survival between the two arms. After adjusting for menopausal status and stage, the relative risk (RR) of recurrence for CMF/EV patients was 0.93 (95% CL 0.64-1.35), while the RR of death was 0.85 (95% CL 0.49-1.47). In conclusion, the Goldie-Coldman model of alternating therapy is not confirmed in this trial of adjuvant therapy of early breast cancer, although in view of its design a difference of less than 20% in 3 year disease-free survival could not be excluded.
本研究的目的是检验戈尔迪和戈德曼的假说,即使用非交叉耐药的化疗方案可带来最大抗肿瘤效果。我们在早期乳腺癌辅助治疗中,将标准CMF(环磷酰胺、甲氨蝶呤、氟尿嘧啶)与交替使用的CMF/EV(表柔比星、长春新碱)进行了比较。II期绝经前淋巴结阳性或绝经后淋巴结阳性、雌激素受体阴性以及III期乳腺癌患者符合本研究条件。1985年1月至1990年12月,220例患者被随机分组(115例接受CMF方案,105例接受CMF/EV方案)。毒性反应较轻;CMF/EV组神经毒性、呕吐和脱发更为常见,而CMF组永久性闭经、腹泻、胃痛和轻度感染更为常见。在48个月的随访中,113例患者(51.4%)出现复发(CMF组62例,CMF/EV组51例),54例(24.5%)死亡(CMF组30例,CMF/EV组24例)。两组在无病生存期和总生存期方面无显著差异。在对绝经状态和分期进行校正后,CMF/EV组患者复发的相对风险(RR)为0.93(95%可信区间0.64 - 1.35),而死亡的RR为0.85(95%可信区间0.49 - 1.47)。总之,在本次早期乳腺癌辅助治疗试验中,未证实戈尔迪 - 戈德曼交替治疗模式,但鉴于其设计,不能排除3年无病生存期差异小于20%的可能性。