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首页> 外文期刊>British Journal of Cancer >A controlled trial of adjuvant tamoxifen, with or without prednisolone, in post-menopausal women with operable breast cancer
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A controlled trial of adjuvant tamoxifen, with or without prednisolone, in post-menopausal women with operable breast cancer

机译:在可手术乳腺癌的绝经后妇女中使用他莫昔芬辅助药物(有或没有泼尼松龙)的对照试验

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A randomised clinical trial has been conducted to compare adjuvant tamoxifen, 20 mg daily, with tamoxifen and prednisolone, 7.5 mg daily, in post-menopausal women with operable breast cancer. There were 254 evaluable patients, of whom 128 were given tamoxifen alone and 126 received tamoxifen and prednisolone. After a median follow-up of 48 months there was no significant difference in relapse-free or overall survival of the two groups. Furthermore, with survival slightly favouring tamoxifen, confidence intervals on the hazard ratio established that a difference in favour of tamoxifen plus prednisolone of even 5% at 5 years was very unlikely (P < 0.02). Thus, despite the relatively small number of patients in this trial, the data clearly establish that prednisolone is not of value as an additional adjuvant agent.
机译:已经进行了一项临床随机试验,比较了可手术乳腺癌的绝经后妇女的他莫昔芬辅助药物(每天20 mg)与他莫昔芬和泼尼松龙(每天7.5 mg)的比较。有254位可评估患者,其中128例单独接受他莫昔芬治疗,126例接受他莫昔芬和泼尼松龙治疗。中位随访48个月后,两组的无复发生存率或总生存率无显着差异。此外,由于生存率稍微偏向于他莫昔芬,因此在危险比上的置信区间确定,在5年内,他莫昔芬与泼尼松龙的偏倚差异甚至很小,仅为5%(P <0.02)。因此,尽管在该试验中患者人数相对较少,但数据清楚地表明泼尼松龙作为附加辅助剂没有价值。

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