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The Efficacy of 3rd Generation Aromatase Inhibitors in Breast Cancer Chemoprevention

机译:第三代芳香化酶抑制剂在乳腺癌化学预防中的功效

摘要

Background: Currently, tamoxifen and raloxifene are the only FDA-approved and USPSTF recommended pharmacologic treatments for breast cancer chemoprevention in high-risk postmenopausal women. Despite their widely recognized efficacy at reducing the incidence of breast cancer, the risk of potentially significant adverse effects may limit patient allocation. Consequently, research on the efficacy of third-generation aromatase inhibitors (AIs) as breast cancer preventives has emerged, especially since their value as adjuvant and combination therapy for breast cancer is well-established. The safety profile of anastrozole and exemestane potentially provide an appealing alternative to postmenopausal patients with a higher risk of developing breast cancer. Studies have successfully demonstrated the efficacy of AIs at reducing the incidence breast cancer, and further research will help to validate the FDA-approval of AIs for this indication.Methods: An exhaustive search of medical literature included MEDLINE, Web of Science, CINAHL, and the National Institute of Health Clinical Trials using the key words: aromatase inhibitors, anastrozole, letrozole, exemestane, and chemoprevention. Relevant articles were critically appraised and GRADE was used for qualitative assessment.Results: An extensive literary search rendered 262 relevant articles from January 2000 to February 2014. After screening several articles, two randomized control trials met inclusion criteria. The NIH clinical trials site yielded 36 results, and one trial met inclusion criteria. The LIBER trial, listed under NCT00673335, is in Phase III with a predicted completion date of February 2017.Conclusion: Third generation AIs, such as anastrozole and exemestane, are very effective at reducing the incidence of invasive breast cancer, ductal carcinoma in situ, and certain tumors in high-risk postmenopausal women. Although both AIs demonstrate adverse effects, their overall safety profiles may be more favorable than other pharmacologic chemoprevention alternatives. More research, larger scale studies, and a longer follow-up after concluding treatment will be valuable to the prospective FDA-approval of AIs in breast cancer prevention.Keywords: aromatase inhibitors, anastrozole, letrozole, exemestane, chemoprevention
机译:背景:目前,他莫昔芬和雷洛昔芬是唯一的FDA批准和USPSTF推荐的高危绝经后妇女乳腺癌化学预防药物疗法。尽管它们在降低乳腺癌发病率方面具有公认的功效,但潜在的重大不良反应的风险可能会限制患者的分配。因此,已经出现了对第三代芳香化酶抑制剂(AIs)作为乳腺癌预防剂的功效的研究,特别是因为它们作为乳腺癌的佐剂和联合疗法的价值已得到公认。阿那曲唑和依西美坦的安全性可能为绝经后的患者提供更高的罹患乳腺癌风险的诱人选择。研究已成功证明了AIs在降低乳腺癌发病率方面的功效,进一步的研究将有助于验证FDA批准的AIs用于该适应症的方法。方法:包括MEDLINE,Web of Science,CINAHL和美国国立卫生研究院临床试验使用的关键词是:芳香化酶抑制剂,阿那曲唑,来曲唑,依西美坦和化学预防。结果:从2000年1月至2014年2月,对262篇相关文章进行了广泛的文献检索。对几篇文章进行筛选后,两项随机对照试验符合纳入标准。 NIH临床试验站点产生了36个结果,其中一项试验符合纳入标准。 LIBER试验处于NCT00673335下,目前处于第三阶段,预计将于2017年2月完成。结论:第三代AI(例如阿那曲唑和依西美坦)在降低浸润性乳腺癌,原位导管癌,和绝经后高危女性中的某些肿瘤。尽管两种AI均显示出不良反应,但它们的总体安全性可能比其他药物化学预防方法更有利。进行更多的研究,更大规模的研究以及结束治疗后的更长随访将对潜在的FDA批准的AI在预防乳腺癌中具有重要意义。关键词:芳香化酶抑制剂,阿那曲唑,来曲唑,依西美坦,化学预防

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    Wogu Katrina;

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