Tan-Chiu Elizabeth, Wang Jiping, Costantino Joseph P, Paik Soonmyung, Butch Cheryl, Wickerham D Lawrence, Fisher Bernard, Wolmark Norman
Cancer Research Network, 350 84th Avenue, Suite 305, Plantation, FL 33324, USA.
J Natl Cancer Inst. 2003 Feb 19;95(4):302-7. doi: 10.1093/jnci/95.4.302.
In 1998 the National Surgical Adjuvant Breast and Bowel Project (NSABP) demonstrated that tamoxifen treatment reduced the incidence of both invasive and noninvasive breast cancer in women at high risk for the disease. We examined the effect of tamoxifen treatment on the incidence of benign breast disease and the number of breast biopsies in the same group of women.
We examined the medical records of 13 203 women with follow-up who participated in the NSABP Breast Cancer Prevention Trial. Included in this analysis were women who had undergone a breast biopsy and who had histologic diagnoses of adenosis, cyst, duct ectasia, fibrocystic disease, fibroadenoma, fibrosis, hyperplasia, or metaplasia. The relative risk (RR) for each histologic diagnosis was estimated for women who received tamoxifen and for women who received placebo. We also tallied the number of biopsies that women in the placebo and tamoxifen groups underwent.
Overall, tamoxifen treatment reduced the risk of benign breast disease by 28% (RR = 0.72, 95% confidence interval [CI] = 0.65 to 0.79). Tamoxifen therapy resulted in statistically significant reductions in the risk of adenosis (RR = 0.59, 95% CI = 0.47 to 0.73), cyst (RR = 0.66, 95% CI = 0.58 to 0.75), duct ectasia (RR = 0.72, 95% CI = 0.53 to 0.97), fibrocystic disease (RR = 0.67, 95% CI = 0.58 to 0.77), hyperplasia (RR = 0.60, 95% CI = 0.50 to 0.71), and metaplasia (RR = 0.51, 95% CI = 0.41 to 0.62). Tamoxifen therapy also reduced the risk for fibroadenoma (RR = 0.77, 95% CI = 0.56 to 1.04) and fibrosis (RR = 0.86, 95% CI = 0.72 to 1.03). Compared with the placebo group, the tamoxifen group had 29% (95% CI = 23% to 34%) fewer biopsies (1048 versus 1469) and 19% fewer women who underwent a biopsy (811 versus 1019). This resulted in a 29% reduction in the risk of biopsy in women treated with tamoxifen (RR = 0.71, 95% CI = 0.66 to 0.77). This risk reduction occurred predominantly in women younger than 50 years.
Women in this study who received tamoxifen, especially younger women (i.e., <50 years), had a reduced incidence of clinically detected benign breast disease and underwent fewer breast biopsies.
1998年,美国国家乳腺与肠道外科辅助治疗项目(NSABP)证实,他莫昔芬治疗可降低患乳腺癌高风险女性浸润性和非浸润性乳腺癌的发病率。我们研究了他莫昔芬治疗对同一组女性良性乳腺疾病发病率及乳房活检次数的影响。
我们查阅了参与NSABP乳腺癌预防试验且有随访记录的13203名女性的病历。纳入该分析的女性均接受过乳房活检,且组织学诊断为腺病、囊肿、导管扩张、纤维囊性疾病、纤维腺瘤、纤维化、增生或化生。分别估算接受他莫昔芬治疗的女性和接受安慰剂治疗的女性每种组织学诊断的相对风险(RR)。我们还统计了安慰剂组和他莫昔芬组女性接受活检的次数。
总体而言,他莫昔芬治疗使良性乳腺疾病风险降低了28%(RR = 0.72,95%置信区间[CI] = 0.65至0.79)。他莫昔芬治疗使腺病风险(RR = 0.59,95% CI = 0.47至 0.73)、囊肿风险(RR = 0.66,95% CI = 0.58至0.75)、导管扩张风险(RR = 0.72,95% CI = 0.53至0.97)、纤维囊性疾病风险(RR = 0.67,95% CI = 0.58至0.77)、增生风险(RR = 0.60,95% CI = 0.50至0.71)和化生风险(RR = 0.51,95% CI = 0.41至0.62)有统计学意义的降低。他莫昔芬治疗还降低了纤维腺瘤风险(RR = 0.77,95% CI = 0.56至1.04)和纤维化风险(RR = 0.86,95% CI = 0.72至1.03)。与安慰剂组相比,他莫昔芬组的活检次数减少了29%(95% CI = 23%至34%)(分别为1048次和1469次),接受活检的女性人数减少了19%(分别为811名和1019名)。这使得接受他莫昔芬治疗的女性活检风险降低了29%(RR = 0.71,95% CI = 0.66至0.77)。这种风险降低主要发生在50岁以下的女性中。
本研究中接受他莫昔芬治疗的女性,尤其是年轻女性(即<50岁),临床检测出的良性乳腺疾病发病率降低,乳房活检次数减少。