Iglesias L, Moreno J A, Torrija E, Murillo E, Codes M, Dugue A, Garcia E, Virizuela J A
Hospital Universitario, Virgen del Rocio, Seville, Spain.
Oncology (Williston Park). 1997 Sep;11(9 Suppl 10):74-81.
Between 1989 and 1993, 409 evaluable patients with breast cancer have been treated with tegafur and uracil (UFT) in an adjuvant setting in two different trials. Data from both trials were reviewed in December 1995 after a mean follow-up of 5.09 +/- 1.1 years (range, 2.9 to 7.1 years). The aim of the first trial was to demonstrate the activity of UFT 400 mg/day for 6 months plus prednimustine 60 mg/m2 for 7 consecutive days, every 28 days in 6 cycles given orally (arm B). This scheme was compared with 6 cycles of cyclophosphamide 600 mg/m2, plus methotrexate 40 mg/m2, plus fluorouracil 600 mg/m2, every 4 weeks (arm A). In this study, 187 premenopausal women were evaluable, 96 in arm A and 91 in arm B, all of whom had positive axillary nodes. Although there were more younger patients in arm A than in arm B, prognostic factors were similar in both groups. Disease-free survival and overall survival were similar in both arms. However, some concern is raised by the low disease-free survival rate. The toxicity was mild (mainly nausea and vomiting and alopecia) and slightly worse in arm A. We believe that oral administration could be a useful alternative to the parenteral route. In the second trial, 222 evaluable patients received 20 mg/day of tamoxifen (Nolvadex) for 1 year (arm A), or the same dose of tamoxifen plus UFT 400 mg/day for 6 months. All patients were postmenopausal, and the characteristics of the tumors were the same as those in patients in the first trial. In arm A there were 109 patients and in arm B, 113. The groups were well balanced. The overall survival and the disease-free survival rates were equal in both arms, but were longer in arm B in the subset of patients with five or more axillary-involved nodes. The toxicity was negligible in both arms. We conclude that UFT/tamoxifen might be useful in postmenopausal patients with five or more involved nodes who are unable to follow a more aggressive schedule because of their age or low performance status.
1989年至1993年期间,409例可评估的乳腺癌患者在两项不同的辅助治疗试验中接受了替加氟尿嘧啶(UFT)治疗。1995年12月,在平均随访5.09±1.1年(范围为2.9至7.1年)后,对两项试验的数据进行了回顾。第一项试验的目的是证明口服UFT 400 mg/天,持续6个月,加用泼尼松龙60 mg/m²,每28天连续7天,共6个周期(B组)的疗效。该方案与每4周给予环磷酰胺600 mg/m²、甲氨蝶呤40 mg/m²、氟尿嘧啶600 mg/m²,共6个周期(A组)进行比较。在这项研究中,187例绝经前女性可评估,A组96例,B组91例,所有患者腋窝淋巴结均为阳性。虽然A组年轻患者比B组多,但两组的预后因素相似。两组的无病生存率和总生存率相似。然而,低无病生存率引发了一些担忧。毒性较轻(主要是恶心、呕吐和脱发),A组稍严重。我们认为口服给药可能是胃肠外给药的一种有用替代方法。在第二项试验中,222例可评估患者接受1年每日20 mg他莫昔芬(诺瓦得士)治疗(A组),或相同剂量的他莫昔芬加UFT 400 mg/天,持续6个月。所有患者均为绝经后,肿瘤特征与第一项试验中的患者相同。A组有109例患者,B组有113例患者。两组平衡良好。两组的总生存率和无病生存率相等,但在腋窝淋巴结受累5个或更多的患者亚组中,B组的生存期更长。两组的毒性均可忽略不计。我们得出结论,UFT/他莫昔芬可能对因年龄或身体状况差而无法接受更积极治疗方案的绝经后腋窝淋巴结受累5个或更多的患者有用。