Veterans Affairs Palo Alto Health Care System, Palo Alto, California.
Stanford University, Stanford, California.
JAMA. 2019 Sep 3;322(9):857-867. doi: 10.1001/jama.2019.11885.
Breast cancer is the most common nonskin cancer among women in the United States and the second leading cause of cancer death. The median age at diagnosis is 62 years, and an estimated 1 in 8 women will develop breast cancer at some point in their lifetime. African American women are more likely to die of breast cancer compared with women of other races.
To update the 2013 US Preventive Services Task Force (USPSTF) recommendation on medications for risk reduction of primary breast cancer.
The USPSTF reviewed evidence on the accuracy of risk assessment methods to identify women who could benefit from risk-reducing medications for breast cancer, as well as evidence on the effectiveness, adverse effects, and subgroup variations of these medications. The USPSTF reviewed evidence from randomized trials, observational studies, and diagnostic accuracy studies of risk stratification models in women without preexisting breast cancer or ductal carcinoma in situ.
The USPSTF found convincing evidence that risk assessment tools can predict the number of cases of breast cancer expected to develop in a population. However, these risk assessment tools perform modestly at best in discriminating between individual women who will or will not develop breast cancer. The USPSTF found convincing evidence that risk-reducing medications (tamoxifen, raloxifene, or aromatase inhibitors) provide at least a moderate benefit in reducing risk for invasive estrogen receptor-positive breast cancer in postmenopausal women at increased risk for breast cancer. The USPSTF found that the benefits of taking tamoxifen, raloxifene, and aromatase inhibitors to reduce risk for breast cancer are no greater than small in women not at increased risk for the disease. The USPSTF found convincing evidence that tamoxifen and raloxifene and adequate evidence that aromatase inhibitors are associated with small to moderate harms. Overall, the USPSTF determined that the net benefit of taking medications to reduce risk of breast cancer is larger in women who have a greater risk for developing breast cancer.
The USPSTF recommends that clinicians offer to prescribe risk-reducing medications, such as tamoxifen, raloxifene, or aromatase inhibitors, to women who are at increased risk for breast cancer and at low risk for adverse medication effects. (B recommendation) The USPSTF recommends against the routine use of risk-reducing medications, such as tamoxifen, raloxifene, or aromatase inhibitors, in women who are not at increased risk for breast cancer. (D recommendation) This recommendation applies to asymptomatic women 35 years and older, including women with previous benign breast lesions on biopsy (such as atypical ductal or lobular hyperplasia and lobular carcinoma in situ). This recommendation does not apply to women who have a current or previous diagnosis of breast cancer or ductal carcinoma in situ.
乳腺癌是美国女性中最常见的非皮肤癌,也是癌症死亡的第二大主要原因。中位诊断年龄为 62 岁,估计每 8 名女性中就有 1 名会在其一生中的某个阶段患上乳腺癌。与其他种族的女性相比,非裔美国女性死于乳腺癌的可能性更高。
更新 2013 年美国预防服务工作组(USPSTF)关于用于降低原发性乳腺癌风险的药物建议。
USPSTF 审查了关于风险评估方法准确性的证据,以确定可以从用于降低乳腺癌风险的药物中获益的女性,以及这些药物的有效性、不良反应和亚组差异的证据。USPSTF 审查了来自没有预先存在的乳腺癌或导管原位癌的女性的随机试验、观察性研究和风险分层模型的诊断准确性研究的证据。
USPSTF 有确凿的证据表明,风险评估工具可以预测预期在人群中发展的乳腺癌病例数。然而,这些风险评估工具在区分将发展或不发展乳腺癌的个体女性方面表现得最好。USPSTF 有确凿的证据表明,降低风险药物(他莫昔芬、雷洛昔芬或芳香化酶抑制剂)在绝经后患有乳腺癌风险增加的女性中,至少能适度降低雌激素受体阳性浸润性乳腺癌的风险。USPSTF 发现,在没有患乳腺癌风险增加的女性中,服用他莫昔芬、雷洛昔芬和芳香化酶抑制剂来降低乳腺癌风险的益处并不大于小。USPSTF 有确凿的证据表明,他莫昔芬和雷洛昔芬以及充分的证据表明,芳香化酶抑制剂与小到中度的危害相关。总体而言,USPSTF 确定,在患有更高乳腺癌风险且不良反应药物风险较低的女性中,服用药物降低乳腺癌风险的净收益更大。
USPSTF 建议临床医生向有乳腺癌风险增加且不良反应药物风险较低的女性提供降低风险的药物,如他莫昔芬、雷洛昔芬或芳香化酶抑制剂。(B 级推荐)USPSTF 建议不要在没有乳腺癌风险增加的女性中常规使用降低风险的药物,如他莫昔芬、雷洛昔芬或芳香化酶抑制剂。(D 级推荐)本建议适用于 35 岁及以上的无症状女性,包括活检有既往良性乳腺病变的女性(如非典型导管或小叶增生和小叶原位癌)。本建议不适用于当前或既往诊断为乳腺癌或导管原位癌的女性。