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五年疗程中他莫昔芬的依从性。

Adherence to tamoxifen over the five-year course.

作者信息

Lash Timothy L, Fox Matthew P, Westrup Jennifer L, Fink Aliza K, Silliman Rebecca A

机构信息

Department of Epidemiology, Boston University School of Public Health, Boston, MA 02118, USA.

出版信息

Breast Cancer Res Treat. 2006 Sep;99(2):215-20. doi: 10.1007/s10549-006-9193-0. Epub 2006 Mar 16.

DOI:10.1007/s10549-006-9193-0
PMID:16541307
Abstract

PURPOSE

To estimate the proportion of older women who fail to complete 5 years of tamoxifen therapy and to identify predictors of non-adherence.

PATIENTS AND METHODS

We followed 462 women 65-years-old or older with stage I-IIIA breast cancer diagnosed in four US regions between 1996 and 1999 and who initiated tamoxifen therapy. We interviewed patients annually to assess tamoxifen adherence and collected information about predictors of adherence by medical record review, patient interview, and physician questionnaire.

RESULTS

Thirty-one percent of patients who started tamoxifen failed to complete the recommended 5-year course. Patients who had initial severe side effects [hazard ratio (HR) per side effect=1.2, 95% confidence interval (CI) 0.97, 1.5] or developed them (HR per new side effect=1.3, 95% CI 1.0, 1.6) were more likely to discontinue. Patients with more prescription medications at baseline were less likely to discontinue (HR per baseline prescription equaled 0.90, 95% CI 0.81, 0.99), whereas patients who added a prescription were more likely to discontinue (HR per new prescription equaled 1.2, 95% CI 1.0, 1.4). Patients with positive views of tamoxifen at baseline (HR for a 10-point higher score=0.93, 95% CI 0.83, 1.0) and an improving view over follow-up (HR for a 10-point positive change=0.93, 95% CI 0.87, 1.0) were less likely to discontinue.

CONCLUSION

Five years of tamoxifen confers a significant benefit beyond 1-2 years of tamoxifen, so physicians should ask patients about side effects, other prescriptions, and beliefs about tamoxifen and should educate them about the benefits of completing adjuvant therapy.

摘要

目的

评估未能完成5年他莫昔芬治疗的老年女性比例,并确定不依从的预测因素。

患者与方法

我们对1996年至1999年间在美国四个地区诊断为I-IIIA期乳腺癌且开始接受他莫昔芬治疗的462名65岁及以上女性进行了随访。我们每年对患者进行访谈以评估他莫昔芬的依从性,并通过病历审查、患者访谈和医生问卷收集有关依从性预测因素的信息。

结果

开始使用他莫昔芬的患者中有31%未能完成推荐的5年疗程。最初出现严重副作用的患者(每个副作用的风险比[HR]=1.2,95%置信区间[CI]0.97,1.5)或出现新副作用的患者(每个新副作用的HR=1.3,95%CI1.0,1.6)更有可能停药。基线时服用更多处方药的患者停药的可能性较小(每个基线处方的HR等于0.90,95%CI0.81,0.99),而增加新处方的患者停药的可能性更大(每个新处方的HR等于1.2,95%CI1.0,1.4)。基线时对他莫昔芬持积极看法的患者(评分每高10分的HR=0.93,95%CI0.83,1.0)以及随访期间看法改善的患者(评分有10分正向变化的HR=0.93,95%CI0.87,1.0)停药的可能性较小。

结论

他莫昔芬服用5年比服用1-2年有显著益处,因此医生应询问患者有关副作用、其他处方以及对他莫昔芬的看法,并应告知他们完成辅助治疗的益处。

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