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他莫昔芬与安慰剂对比:老年II期乳腺癌女性的双盲辅助试验。

Tamoxifen versus placebo: double-blind adjuvant trial in elderly women with stage II breast cancer.

作者信息

Cummings F J, Gray R, Davis T E, Tormey D C, Harris J E, Falkson G G, Arseneau J

出版信息

NCI Monogr. 1986(1):119-23.

PMID:3534584
Abstract

One hundred eighty-one elderly women with stage II breast cancer were prospectively randomized to receive tamoxifen or placebo for 24 months in a double-blind adjuvant trial conducted by the Eastern Cooperative Oncology Group. They were stratified prior to randomization on the basis of the number of positive axillary nodes and the estrogen receptor status of their primary tumor. One hundred seventy were considered eligible and analyzed in this trial. The median age was 71 years with a range from 65 to 84 years. Twenty-one percent of the patients were over the age of 75 and 33% were between 71 and 75 years. Estrogen receptor status was positive in 85% of the patients and unknown in another 12%. Progesterone receptor status was positive in 35%, negative in 16%, and unknown in 49%. With a median follow-up of 55 months, the overall percent disease free at 4 years is 73 for the tamoxifen arm and 52 for the placebo arm (P = .003). Significant benefit is seen following tamoxifen in the subsets with 4-10 positive axillary lymph nodes, those who were estrogen receptor positive, or progesterone receptor unknown, and those who had a tumor size less than 3 cm. Most other subsets benefited as well. There were more distant (29 vs. 13) and bone only (15 vs. 3) sites of first recurrence in the placebo arm, whereas locoregional recurrences were similar (8 each). The recorded toxicity was similar, except for more hot flashes observed among women in the tamoxifen arm.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

在东部肿瘤协作组开展的一项双盲辅助试验中,181名II期乳腺癌老年女性被前瞻性随机分组,接受他莫昔芬或安慰剂治疗24个月。她们在随机分组前根据腋窝阳性淋巴结数量和原发肿瘤的雌激素受体状态进行了分层。本试验纳入170名符合条件的患者并进行分析。中位年龄为71岁,范围在65至84岁之间。21%的患者年龄超过75岁,33%的患者年龄在71至75岁之间。85%的患者雌激素受体状态为阳性,另有12%未知。35%的患者孕激素受体状态为阳性,16%为阴性,49%未知。中位随访55个月后,他莫昔芬组4年时的总体无病百分比为73%,安慰剂组为52%(P = 0.003)。在腋窝淋巴结4 - 10个阳性、雌激素受体阳性或孕激素受体未知以及肿瘤大小小于3 cm的亚组中,他莫昔芬治疗后有显著益处。大多数其他亚组也从中获益。安慰剂组首次复发的远处部位(29个 vs. 13个)和仅骨转移部位(15个 vs. 3个)更多,而局部区域复发相似(各8个)。记录的毒性相似,只是他莫昔芬组女性出现潮热的情况更多。(摘要截选至250字)

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