首页> 美国卫生研究院文献>The Journal of Pharmacy Technology : jPT : Official Publication of the Association of Pharmacy Technicians >Retrospective Study of the Prevalence Predictors and Consequencesof Nonadherence With Lapatinib in Women With Metastatic Breast Cancer Who WerePreviously Treated With Trastuzumab
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Retrospective Study of the Prevalence Predictors and Consequencesof Nonadherence With Lapatinib in Women With Metastatic Breast Cancer Who WerePreviously Treated With Trastuzumab

机译:患病率预测因素和后果的回顾性研究拉帕替尼不依从性在转移性乳腺癌患者中的作用以前用曲妥珠单抗治疗

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摘要

>Background. Lapatinib is an oral small molecule dual tyrosine kinase inhibitor that has been shown to improve time to progression versus capecitabine in women with HER2+ metastatic breast cancer (MBC) previously treated with trastuzumab. >Objective. To describe extent, predictors, and consequences of nonadherence with lapatinib in women with MBC who were previously treated with trastuzumab. >Methods. This was a retrospective observational study using data from a large health insurance claims databases spanning January 2000 to March 2010. Measures of lapatinib adherence included medication possession ratio (MPR), time to discontinuation (end of supply), time to first treatment interruption (gap during treatment of 30 days without supply), and duration of continuous therapy (time to gap of 30 days without supply or end of supply). Predictors of nonadherence to lapatinib and the association between nonadherence and outcomes, utilization, and costs were examined using multiple regression analysis. >Results. A total of 666 patients met all inclusion criteria. Mean initial lapatinib dosage was 1161 mg daily; 63% received index lapatinib in combination with capecitabine. Mean MPR was 87%; 22% of patients had MPR < 80%. Median time to lapatinibdiscontinuation was 9.1 months (95% confidence interval = 8.0-10.2).Twenty-seven percent of patients had one or more treatment interruptions duringfollow-up. Median duration of continuous therapy was 5.9 months (95% confidenceinterval = 5.1-6.1). Concomitant therapy with a taxane was a predictor ofnonadherence (odds ratio for MPR < 80% = 10.30; P <.001). There was a statistically significant association between nonadherence tolapatinib and greater number of outpatient visits (P = .028).>Conclusions. In women with MBC who were previously treated withtrastuzumab, mean adherence to lapatinib in typical clinical practice isrelatively high overall, although there is a small group of patients with highnonadherence. Targeted efforts to improve adherence to lapatinib in thissubgroup may be warranted.
机译:>背景。拉帕替尼是一种口服小分子双酪氨酸激酶抑制剂,已显示与卡培他滨相比,以前用曲妥珠单抗治疗的HER2 +转移性乳腺癌(MBC)的妇女可改善进展时间。 >目的。描述先前接受曲妥珠单抗治疗的MBC患者中拉帕替尼不依从的程度,预测因素和后果。 >方法。这是一项回顾性观察性研究,使用了来自2000年1月至2010年3月的大型健康保险理赔数据库中的数据。拉帕替尼依从性的衡量标准包括药物拥有率(MPR),停药时间(供应终止) ),首次治疗中断的时间(在没有供应的情况下30天的治疗间隔)和持续治疗的持续时间(到没有供应或供应结束的30天的间隔时间)。使用多元回归分析检查了拉帕替尼不依从性的预测因素以及不依从性与结果,利用率和成本之间的关联。 >结果。总共666名患者符合所有纳入标准。拉帕替尼初始平均剂量为每日1161 mg; 63%的患者接受拉帕替尼联合卡培他滨治疗的指数。平均MPR为87%; 22%的患者MPR <80%。拉帕替尼的中位时间停药时间为9.1个月(95%置信区间= 8.0-10.2)。27%的患者在治疗期间出现了一次或多次治疗中断跟进。持续治疗的中位时间为5.9个月(95%的置信度间隔= 5.1-6.1)。紫杉烷类药物的联合治疗是不粘连(MPR <80%的赔率= 10.30; P <.001)。依从性与不依从性之间存在统计上的显着关联拉帕替尼和更多的门诊就诊次数(P = .028)。>结论。在先前接受过MBC治疗的女性中曲妥珠单抗,在典型的临床实践中平均遵守拉帕替尼总体上相对较高,尽管有一小部分患者不遵守。在此方面有针对性地努力提高对拉帕替尼的依从性亚组可能是有保证的。

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