Kaufmann Manfred, Graf Erika, Jonat Walter, Eiermann Wolfgang, Vescia Sabine, Geberth Matthias, Conrad Bettina, Gademann Günther, Albert Ute-Susann, Loibl Sibylle, von Minckwitz Gunter, Schumacher Martin
Universitäts-Frauenklinik, Theodor-Stern-Kai 7, 60596 Frankfurt, Germany.
Eur J Cancer. 2007 Nov;43(16):2351-8. doi: 10.1016/j.ejca.2007.08.012. Epub 2007 Sep 25.
GABG-IV B-93 is a prospective, randomised study comparing goserelin (n=384) with no further treatment (n=392) in hormone receptor (HR)-negative breast cancer patients (n=465) after 3 cycles cyclophosphamide, methotrexate, 5-fluorouracil (CMF) for patients with 0-3 positive lymph nodes (LN) or 4 cycles epirubicin, cyclophosphamide (EC) followed by 3 cycles CMF for patients with 4-9 positive LN. After completion of the ZEBRA trial the study was amended to enrol also HR-positive patients with 1-9+LN (n=311). After a median follow-up of 4.7 years neither HR-negative nor HR-positive patients showed a benefit for goserelin. The adjusted estimated hazard ratio for event-free survival in HR-negative patients was 1.01 (goserelin versus control, 95% confidence interval [CI] 0.72-1.42, P=0.97) and 0.77 in HR-positive patients (95% CI 0.47-1.24, P=0.27). These results do not support the general use of goserelin after adjuvant chemotherapy in this group of premenopausal patients.
GABG-IV B-93是一项前瞻性随机研究,在0至3个阳性淋巴结(LN)的患者接受3个周期环磷酰胺、甲氨蝶呤、5-氟尿嘧啶(CMF)或4至9个阳性LN的患者接受4个周期表柔比星、环磷酰胺(EC)随后3个周期CMF治疗后,比较戈舍瑞林(n = 384)与不进行进一步治疗(n = 392)在激素受体(HR)阴性乳腺癌患者(n = 465)中的效果。在ZEBRA试验完成后,该研究进行了修正,纳入了1至9个以上LN的HR阳性患者(n = 311)。经过4.7年的中位随访,HR阴性和HR阳性患者均未显示戈舍瑞林有获益。HR阴性患者无事件生存的调整后估计风险比为1.01(戈舍瑞林与对照组相比,95%置信区间[CI] 0.72 - 1.42,P = 0.97),HR阳性患者为0.77(95% CI 0.47 - 1.24,P = 0.27)。这些结果不支持在这组绝经前患者辅助化疗后常规使用戈舍瑞林。