首页> 外文期刊>Acta Haematologica >Medication Adherence to Tyrosine Kinase Inhibitors: 2-Year Analysis of Medication Adherence to Imatinib Treatment for Chronic Myeloid Leukemia and Correlation with the Depth of Molecular Response
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Medication Adherence to Tyrosine Kinase Inhibitors: 2-Year Analysis of Medication Adherence to Imatinib Treatment for Chronic Myeloid Leukemia and Correlation with the Depth of Molecular Response

机译:酪氨酸激酶抑制剂的药物依从性:对伊马替尼治疗慢性粒细胞白血病药物依从性的2年分析及其与分子反应深度的关系

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Objective: Adherence to tyrosine kinase inhibitor treatment is a significant factor in the achievement of a good clinical response in chronic myeloid leukemia (CML). The aim of this retrospective study is to investigate 1- and 2-year medication adherence to imatinib treatment, linking adherence rates with the clinical outcome, in accordance with European LeukemiaNet Recommendations for the management of CML. We have tried to find a cutoff value for adherence in order to achieve a good clinical outcome. Methods: The method used to calculate medication adherence was the ratio between the received and the prescribed daily dose. Results: We observed the levels of mean adherence for each of the following response groups (in years 1 and 2, respectively): complete response (0.96, 0.95), MR4.5 (1.00,-), MR4 (0.93, 0.91), major molecular responses (0.96, 0.97), warning (0.91, 0.89) and failure (0.79, 0.84). Conclusion: Results show that the higher the adherence, the lower the level of BCR-ABL1. Furthermore, using cutoffs >= 0.9, outcomes were significantly improved compared to those with cutoffs <0.90. This value of adherence is in line with previous publications. (C) 2016 S. Karger AG, Basel
机译:目的:坚持酪氨酸激酶抑制剂治疗是实现慢性粒细胞白血病(CML)良好临床反应的重要因素。这项回顾性研究的目的是根据欧洲LeukemiaNet对CML管理的建议,研究依马替尼治疗1年和2年药物依从性,并将依从率与临床结果联系起来。我们试图找到依从性的临界值,以达到良好的临床效果。方法:用于计算药物依从性的方法是所接收的剂量与处方的每日剂量之比。结果:我们观察了以下每个应答组(分别在第1年和第2年)的平均依从性水平:完全应答(0.96、0.95),MR4.5(1.00,-),MR4(0.93、0.91),主要分子响应(0.96,0.97),警告(0.91、0.89)和失败(0.79,0.84)。结论:结果表明,依从性越高,BCR-ABL1的水平越低。此外,与截止值<0.90相比,使用截止值> = 0.9的结果显着改善。坚持的价值与以前的出版物一致。 (C)2016 S.Karger AG,巴塞尔

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