From the Department of Population Health Sciences, Huntsman Cancer Institute, University of Utah, Salt Lake City, UT.
Department of Biostatistics and Bioinformatics, Rollins School of Public Health, Emory University, Atlanta, GA.
Epidemiology. 2024 Sep 1;35(5):660-666. doi: 10.1097/EDE.0000000000001753. Epub 2024 Aug 6.
Breast cancer has an average 10-year relative survival reaching 84%. This favorable survival is due, in part, to the introduction of biomarker-guided therapies. We estimated the population-level effect of the introduction of two adjuvant therapies-tamoxifen and trastuzumab-on recurrence using the trend-in-trend pharmacoepidemiologic study design.
We ascertained data on women diagnosed with nonmetastatic breast cancer who were registered in the Danish Breast Cancer Group clinical database. We used the trend-in-trend design to estimate the population-level effect of the introduction of (1) tamoxifen for postmenopausal women with estrogen receptor (ER)-positive breast cancer in 1982, (2) tamoxifen for premenopausal women diagnosed with ER-positive breast cancer in 1999, and (3) trastuzumab for women <60 years diagnosed with human epidermal growth factor receptor 2-positive breast cancer in 2007.
For the population-level effect of the introduction of tamoxifen among premenopausal women diagnosed with ER-positive breast cancer in 1999, the risk of recurrence decreased by nearly one-half (OR = 0.52), consistent with evidence from clinical trials; however, the estimate was imprecise (95% confidence interval [CI] = 0.25, 1.85). We observed an imprecise association between tamoxifen use and recurrence from the time it was introduced in 1982 (OR = 1.24 95% CI = 0.46, 5.11), inconsistent with prior knowledge from clinical trials. For the introduction of trastuzumab in 2007, the estimate was also consistent with trial evidence, though imprecise (OR = 0.51; 95% CI = 0.21, 22.4).
We demonstrated how novel pharmacoepidemiologic analytic designs can be used to evaluate the routine clinical care and effectiveness of therapeutic advancements in a population-based setting while considering some limitations of the approach.
乳腺癌的 10 年相对生存率平均达到 84%。这种良好的生存结果部分归因于生物标志物指导治疗的引入。我们采用趋势内趋势药物流行病学研究设计,估计两种辅助治疗药物——他莫昔芬和曲妥珠单抗的引入对复发的人群水平影响。
我们确定了在丹麦乳腺癌组临床数据库中登记的患有非转移性乳腺癌的女性的数据。我们使用趋势内趋势设计来估计 1982 年他莫昔芬用于绝经后雌激素受体(ER)阳性乳腺癌患者、1999 年他莫昔芬用于绝经前 ER 阳性乳腺癌患者以及 2007 年曲妥珠单抗用于诊断为人类表皮生长因子受体 2 阳性乳腺癌且年龄<60 岁的女性的引入对人群水平的影响。
对于 1999 年诊断为 ER 阳性乳腺癌的绝经前女性引入他莫昔芬的人群水平效果,复发风险降低近一半(OR=0.52),与临床试验证据一致;然而,估计结果不够精确(95%置信区间[CI]:0.25,1.85)。我们观察到他莫昔芬从 1982 年开始使用与复发之间存在不精确的关联(OR=1.24,95%CI:0.46,5.11),与临床试验的先前知识不一致。对于 2007 年曲妥珠单抗的引入,估计结果也与试验证据一致,但不够精确(OR=0.51;95%CI:0.21,22.4)。
我们展示了如何在人群基础上使用新的药物流行病学分析设计来评估常规临床护理和治疗进展的有效性,同时考虑到该方法的一些局限性。