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绝经后乳腺癌患者的辅助内分泌治疗:激素受体状态是否影响决策?

Adjuvant endocrine therapy in postmenopausal breast cancer patients: does hormone receptor status influence decision-making?

机构信息

Department of Medical Oncology, University Hospital of Udine, Udine, Italy.

出版信息

Crit Rev Oncol Hematol. 2011 Feb;77(2):87-99. doi: 10.1016/j.critrevonc.2010.01.006. Epub 2010 Feb 4.

Abstract

Hormonal therapy, such as tamoxifen (TAM), is the cornerstone of adjuvant treatment for women with surgically resected early breast cancer that is hormone receptor-positive (HR+), typically defined by breast tumors that express the estrogen receptor (ER), the progesterone receptor (PgR), or both. TAM can have both estrogen-antagonistic and estrogen-agonistic effects, and expression of growth factor receptors such as human epidermal growth factor receptor (HER)2 in breast cancer is associated with the development of TAM resistance. Studies also suggest that a lack of PgR expression in tumors with positive ER status may be associated with increased growth factor expression, a more aggressive tumor phenotype, and TAM resistance. The aromatase inhibitors (AIs) anastrozole, letrozole, and exemestane have proven more effective than TAM as adjuvant hormonal therapy in postmenopausal women with HR+ disease. Some translational studies have also begun to investigate the efficacy of hormonal therapy according to PgR or HER2 status of the tumor. The AIs have proven to be an attractive option for patients across a broad spectrum of receptor expression profiles, and the potential for combination therapy using AIs and specific growth factor inhibitors is also under investigation.

摘要

激素治疗,如他莫昔芬(TAM),是手术切除的激素受体阳性(HR+)早期乳腺癌辅助治疗的基石,通常定义为表达雌激素受体(ER)、孕激素受体(PgR)或两者均表达的乳腺肿瘤。TAM 具有雌激素拮抗和雌激素激动作用,乳腺癌中生长因子受体如人表皮生长因子受体(HER)2 的表达与 TAM 耐药的发展相关。研究还表明,ER 阳性肿瘤中缺乏 PgR 表达可能与生长因子表达增加、更具侵袭性的肿瘤表型和 TAM 耐药相关。芳香酶抑制剂(AIs)阿那曲唑、来曲唑和依西美坦已被证明比 TAM 作为 HR+疾病绝经后妇女的辅助激素治疗更有效。一些转化研究也开始根据肿瘤的 PgR 或 HER2 状态研究激素治疗的疗效。AIs 已被证明是受体表达谱广泛的患者的一种有吸引力的选择,并且正在研究使用 AIs 和特定生长因子抑制剂的联合治疗的潜力。

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