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Persistence in patients with breast cancer treated with tamoxifen or aromatase inhibitors: A retrospective database analysis

机译:他莫昔芬或芳香化酶抑制剂治疗的乳腺癌患者的持久性:回顾性数据库分析

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Compliance and persistence are often underestimated in breast cancer (BC) treatment. The aim of our study was to analyze the persistence with tamoxifen (TAM) and aromatase inhibitors (AI) in postmenopausal women with hormone-receptor-positive BC and to identify determinants of non-persistence. We used data of the Disease Analyzer database (IMS HEALTH, Germany) including 2,067 general practices and 397 gynecological practices. Out of a dataset of 15 million patients, we identified BC patients with a first-time TAM or AI prescriptions from October 2001 to December 2010. For persistence analyses, 12,412 women on tamoxifen, 2,796 on anastrozole, 647 on exemestane, and 1,657 on letrozole met the inclusion/exclusion criteria. Within 3 years of follow-up, the discontinuation rates increased to 52.2 % for tamoxifen, 47 % for anastrozole, 55.1 % for exemestane, and 44.3 % for letrozole treated women. A minor proportion of patients switched to a different endocrine treatment; 33 % tamoxifen, 20 % anastrozole, 22.9 % exemestane, and 23 % letrozole. The multivariate hazard ratios of the cox regression models showed that patients younger than 50 were most likely to discontinue initial therapy when compared with the reference group of women over 70 (p < 0.001). In contrast, patients treated in gynecologist practice had significantly longer persistence than patients who obtained their prescriptions in general practitioner practice (p < 0.001). In addition, the presence of the co morbidities like diabetes (p < 0.001) or depression (p < 0.002) was also associated with decreased risk of treatment discontinuation. Persistence with all endocrine treatments in women with hormone-receptor-positive BC is low and needs to be significantly increased to improved outcome in clinical practice. Further research is required to understand this complex issue. ? 2013 Springer Science+Business Media New York.
机译:在乳腺癌(BC)治疗中,依从性和持久性常常被低估。我们研究的目的是分析他莫昔芬(TAM)和芳香化酶抑制剂(AI)在绝经后激素受体阳性BC妇女中的持久性,并确定非持久性的决定因素。我们使用了疾病分析器数据库(德国IMS HEALTH)的数据,其中包括2,067个常规操作和397个妇科操作。在1500万患者的数据集中,我们从2001年10月至2010年12月确定了具有首次TAM或AI处方的BC患者。为进行持续性分析,他莫昔芬使用12,412名妇女,阿那曲唑使用2,796名妇女,依西美坦使用647名,来曲唑使用1,657名符合纳入/排除标准。在随访的三年内,他莫昔芬,阿那曲唑的47%,依西美坦的55.1%和来曲唑治疗的妇女的停药率增加到52.2%。少数患者改用其他内分泌治疗; 33%他莫昔芬,20%阿那曲唑,22.9%依西美坦和23%来曲唑。 Cox回归模型的多元风险比表明,与参考组的70岁以上女性相比,年龄小于50岁的患者最有可能中断初始治疗(p <0.001)。相比之下,接受妇科医生治疗的患者的持久性要比接受全科医生实践的患者的持久性长得多(p <0.001)。此外,糖尿病(p <0.001)或抑郁(p <0.002)等合并症的存在也与治疗中止风险降低有关。激素受体阳性的BC妇女所有内分泌治疗的持久性均较低,需要显着增加以改善临床实践的预后。需要进一步的研究来理解这个复杂的问题。 ? 2013年Springer Science + Business Media纽约。

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