Department of Clinical Science and Education at Södersjukhuset, Karolinska Institutet, Department of Oncology, Södersjukhuset, Stockholm, Sweden.
Department of Laboratory Medicine, Clinical Pharmacology, Karolinska Institutet and Medical Diagnostics, Karolinska University Hospital, Stockholm, Sweden.
Breast Cancer Res Treat. 2023 Apr;198(3):499-508. doi: 10.1007/s10549-023-06887-2. Epub 2023 Mar 1.
Suboptimal adherence to adjuvant endocrine treatment (AET) is an important clinical concern. A correlation between CYP2D6 activity and tamoxifen discontinuation has been described. The main aim of this study was to investigate the consistency between pharmacy dispensation data and medical records on adherence to AET.
Adherence was calculated for patients with at least 4.5 years of follow up and was defined as Medical Possession Rate ≥ 80%. Subgroup analyses were performed based on menopausal status, recurrence risk and CYP2D6 activity.
In 86% of the 1235 included patients the consistency between the two sources of information was within 80-125%. Poor consistency, < 80%, was most frequent in the premenopausal/ high-risk group and CYP2D6 Poor Metabolizers (PMs). Among 899 patients with at least 4.5 years follow up, 72% were adherent to tamoxifen based on pharmacy dispensation data, compared with 77% as reported by medical records. When including patients who switched to aromatase inhibitors after tamoxifen, adherence increased to 82% and 88%, respectively. Adherence did not differ by menopausal status or risk for recurrence. CYP2D6 PMs had poorer adherence (54%) to tamoxifen compared to patients with the highest CYP2D6 activity (83%).
There was a good consistency between medical records and pharmacy dispensing data on the use of AET. Adherence to AET was adequate, especially when including switch to aromatase inhibitors. Surprisingly, CYP2D6 PMs had low adherence to tamoxifen, despite a likely reduced risk of side effects according to previous data.
辅助内分泌治疗(AET)的依从性不理想是一个重要的临床问题。已经描述了 CYP2D6 活性与他莫昔芬停药之间的相关性。本研究的主要目的是研究药房配药数据与 AET 依从性的医疗记录之间的一致性。
对至少随访 4.5 年的患者进行了依从性计算,定义为药物利用率(MPR)≥80%。根据绝经状态、复发风险和 CYP2D6 活性进行了亚组分析。
在 1235 名纳入患者中,86%的患者两种信息来源的一致性在 80-125%之间。一致性差,<80%,最常见于绝经前/高危组和 CYP2D6 弱代谢者(PMs)。在 899 名至少随访 4.5 年的患者中,根据药房配药数据,72%的患者对他莫昔芬的依从性,而医疗记录报告的为 77%。当包括在他莫昔芬后转为芳香化酶抑制剂的患者时,依从性分别增加到 82%和 88%。依从性与绝经状态或复发风险无关。与 CYP2D6 活性最高的患者(83%)相比,CYP2D6 PM 患者对他莫昔芬的依从性较差(54%)。
AET 使用方面,医疗记录和药房配药数据之间具有良好的一致性。AET 的依从性充足,特别是包括转为芳香化酶抑制剂时。令人惊讶的是,尽管根据先前的数据,CYP2D6 PM 患者发生副作用的风险可能降低,但他们对他莫昔芬的依从性较低。