Partridge Ann H, Wang Philip S, Winer Eric P, Avorn Jerry
Department of Medical Oncology, Dana-Farber Cancer Institute, 44 Binney Street, D1210, Boston, MA 02215, USA.
J Clin Oncol. 2003 Feb 15;21(4):602-6. doi: 10.1200/JCO.2003.07.071.
Although clinical trials have clearly demonstrated the benefits of tamoxifen in women with primary breast cancer, little is known about how this drug is actually used in the general population. We sought to estimate adherence and predictors of nonadherence in women starting tamoxifen as adjuvant breast cancer therapy.
Subjects were age 18 years or older initiating tamoxifen for primary breast cancer and enrolled in New Jersey's Medicaid or Pharmaceutical Assistance to the Aged and Disabled programs during the study period, from 1990 to 1996 (N = 2,378). Main outcome measures were number of days covered by filled prescriptions for tamoxifen in the first year of therapy with the 4 years after tamoxifen initiation for a subset; predictors of good versus poor adherence.
Twenty-three percent of patients missed taking tamoxifen on more than one fifth of days studied, although on average, patients filled prescriptions for tamoxifen for 87% of their first year of treatment. The youngest, oldest, nonwhite, and mastectomy patients had significantly lower rates of adherence; patients who had seen an oncologist before taking tamoxifen had significantly higher rates of adherence. Overall adherence decreased to 50% by year 4 of therapy.
The mean level of adherence to tamoxifen is high compared with other chronic medications. However, nearly one fourth of patients may be at risk for inadequate clinical response because of poor adherence. Because of the efficacy of tamoxifen therapy in preventing recurrence and death in women with early-stage breast cancer, further efforts are necessary to identify and prevent suboptimal adherence.
尽管临床试验已明确证明他莫昔芬对原发性乳腺癌女性患者有益,但对于该药物在普通人群中的实际使用情况却知之甚少。我们试图评估开始使用他莫昔芬作为辅助性乳腺癌治疗的女性患者的依从性及其不依从的预测因素。
研究对象为年龄在18岁及以上、开始使用他莫昔芬治疗原发性乳腺癌且在1990年至1996年研究期间参加新泽西州医疗补助计划或老年人及残疾人药物援助计划的患者(N = 2378)。主要观察指标为治疗第一年他莫昔芬处方配药覆盖的天数,以及对一部分患者在开始使用他莫昔芬后的4年里的情况;依从性良好与不佳的预测因素。
23%的患者在所研究的超过五分之一的天数里未服用他莫昔芬,不过平均而言,患者在治疗的第一年里有87%的时间配取了他莫昔芬处方。最年轻、最年长、非白人以及接受乳房切除术的患者依从率显著较低;在服用他莫昔芬之前看过肿瘤内科医生的患者依从率显著较高。到治疗第4年时,总体依从率降至50%。
与其他慢性药物相比,他莫昔芬的平均依从水平较高。然而,近四分之一的患者可能因依从性差而面临临床反应不足的风险。鉴于他莫昔芬治疗在预防早期乳腺癌女性患者复发和死亡方面的疗效,有必要进一步努力识别并防止依从性欠佳的情况。