Institut Gustave Roussy, Villejuif, France.
Université Paris-Saclay, Faculté de Pharmacie, Saint-Aubin, France.
J Clin Oncol. 2020 Aug 20;38(24):2762-2772. doi: 10.1200/JCO.19.01758. Epub 2020 Jun 22.
Nonadherence to long-term treatments is often under-recognized by physicians and there is no gold standard for its assessment. In breast cancer, nonadherence to tamoxifen therapy after surgery constitutes a major obstacle to optimal outcomes. We sought to evaluate the rate of biochemical nonadherence to adjuvant tamoxifen using serum assessment and to examine its effects on short-term, distant disease-free survival (DDFS).
We studied 1,177 premenopausal women enrolled in a large prospective study (CANTO/NCT01993498). Definition of biochemical nonadherence was based on a tamoxifen serum level < 60 ng/mL, assessed 1 year after prescription. Self-reported nonadherence to tamoxifen therapy was collected at the same time through semistructured interviews. Survival analyses were conducted using an inverse probability weighted Cox proportional hazards model, using a propensity score based on age, staging, surgery, chemotherapy, and center size.
Serum assessment of tamoxifen identified 16.0% of patients (n = 188) below the set adherence threshold. Patient-reported rate of nonadherence was lower (12.3%). Of 188 patients who did not adhere to the tamoxifen prescription, 55% self-reported adherence to tamoxifen. After a median follow-up of 24.2 months since tamoxifen serum assessment, patients who were biochemically nonadherent had significantly shorter DDFS (for distant recurrence or death, adjusted hazard ratio, 2.31; 95% CI, 1.05 to 5.06; = .036), with 89.5% of patients alive without distant recurrence at 3 years in the nonadherent cohort versus 95.4% in the adherent cohort.
Therapeutic drug monitoring may be a useful method to promptly identify patients who do not take adjuvant tamoxifen as prescribed and are at risk for poorer outcomes. Targeted interventions facilitating patient adherence are needed and have the potential to improve short-term breast cancer outcomes.
长期治疗的不依从常常被医生所忽视,并且目前还没有评估其的金标准。在乳腺癌中,手术后对他莫昔芬治疗的不依从是影响最佳治疗效果的主要障碍。我们旨在通过血清评估来评估辅助他莫昔芬治疗的生化不依从率,并探讨其对短期无远处疾病生存(DDFS)的影响。
我们研究了入组于一项大型前瞻性研究(CANTO/NCT01993498)的 1177 例绝经前女性。生化不依从的定义为他莫昔芬血清水平<60ng/mL,在处方后 1 年评估。通过半结构式访谈同时收集他莫昔芬治疗的自我报告不依从情况。使用逆概率加权 Cox 比例风险模型进行生存分析,使用基于年龄、分期、手术、化疗和中心规模的倾向评分。
通过他莫昔芬的血清评估发现,16.0%(n=188)的患者低于设定的依从阈值。而患者报告的不依从率较低(12.3%)。在 188 例未按他莫昔芬处方服药的患者中,有 55%的患者报告自己遵医嘱服用了他莫昔芬。在进行他莫昔芬血清评估后中位随访 24.2 个月时,生化不依从的患者 DDFS 明显更短(远处复发或死亡的调整后的危险比为 2.31;95%CI,1.05~5.06;P=0.036),不依从组有 89.5%的患者在 3 年内无远处复发,而依从组有 95.4%。
治疗药物监测可能是一种有用的方法,可及时识别未按规定服用辅助他莫昔芬且预后不良风险较高的患者。需要采取针对性的干预措施来促进患者的依从性,这可能会改善短期乳腺癌的治疗效果。