Kinsinger Linda S, Harris Russell, Woolf Steven H, Sox Harold C, Lohr Kathleen N
Cecil G. Sheps Center for Health Services Research, Program on Prevention, CB# 7508, Wing D, Room 383, University of North Carolina School of Medicine, Chapel Hill, NC 27599-7508, USA.
Ann Intern Med. 2002 Jul 2;137(1):59-69. doi: 10.7326/0003-4819-137-1-200207020-00017.
Chemoprevention offers promise as a strategy for reducing morbidity and mortality from breast cancer in women. This review examined the evidence for the effectiveness of chemoprevention in women without a history of breast cancer.
MEDLINE (1966 to December 2001).
English-language, randomized, controlled trials (RCTs) of chemoprevention of breast cancer in women without a previous diagnosis of breast cancer were examined, and 4 relevant trials, 3 involving tamoxifen and 1 involving raloxifene, were selected. Trials that provided data on the harms of tamoxifen or raloxifene, studies of the costs of chemoprevention, and studies of risk assessment were also reviewed.
Four reviewers independently abstracted data on key variables, including study population, sample size, randomization, treatment, and outcomes.
The largest of the RCTs of tamoxifen reported a 49% reduction in relative risk (0.51 [95% CI, 0.39 to 0.66]) for invasive cancer among women with an estimated 5-year breast cancer risk of at least 1.66%. The other tamoxifen trials did not observe a statistically significant benefit, but only a few women in each trial took tamoxifen during the entire study period. The raloxifene study of postmenopausal women with osteoporosis found a 76% reduction in relative risk (0.24 [CI, 0.13 to 0.44]) for invasive breast cancer. Tamoxifen and raloxifene were effective only against estrogen receptor-positive tumors. Both drugs increased risk for venous thromboembolic disease and hot flashes; tamoxifen increased risk for endometrial cancer and stroke.
Tamoxifen and raloxifene reduce the incidence of estrogen receptor-positive breast cancer in women. The relative risk reduction seems similar across all breast cancer risk groups. The absolute risk reduction varies by risk factors for breast cancer, however, and must be balanced against the potential harms to judge the appropriateness of treatment for individual women.
化学预防作为降低女性乳腺癌发病率和死亡率的一种策略具有前景。本综述考察了无乳腺癌病史女性中化学预防有效性的证据。
MEDLINE(1966年至2001年12月)。
对未患过乳腺癌女性进行乳腺癌化学预防的英文随机对照试验(RCT)进行考察,选取了4项相关试验,3项涉及他莫昔芬,1项涉及雷洛昔芬。还对提供他莫昔芬或雷洛昔芬危害数据的试验、化学预防成本研究以及风险评估研究进行了综述。
4名审阅者独立提取关键变量的数据,包括研究人群、样本量、随机分组、治疗及结果。
他莫昔芬最大规模的RCT报告显示,估计5年乳腺癌风险至少为1.66%的女性中,浸润性癌的相对风险降低了49%(0.51[95%CI,0.39至0.66])。其他他莫昔芬试验未观察到统计学上的显著益处,但每项试验中只有少数女性在整个研究期间服用他莫昔芬。对患有骨质疏松症的绝经后女性进行的雷洛昔芬研究发现,浸润性乳腺癌的相对风险降低了76%(0.24[CI,0.13至0.44])。他莫昔芬和雷洛昔芬仅对雌激素受体阳性肿瘤有效。两种药物均增加了静脉血栓栓塞性疾病和潮热的风险;他莫昔芬增加了子宫内膜癌和中风的风险。
他莫昔芬和雷洛昔芬可降低女性雌激素受体阳性乳腺癌的发病率。所有乳腺癌风险组的相对风险降低似乎相似。然而,绝对风险降低因乳腺癌风险因素而异,必须与潜在危害相权衡,以判断对个体女性治疗的适宜性。