UPMC Hillman Cancer Center, University of Pittsburgh Medical Center, Pittsburgh, PA, USA.
Division of Research, Kaiser Permanente Northern California, Oakland, CA, USA.
Breast Cancer Res Treat. 2024 Nov;208(2):223-235. doi: 10.1007/s10549-024-07469-6. Epub 2024 Aug 23.
Cyclin-dependent kinase 4/6 inhibitors (CDK4/6i) have improved patient survival in hormone receptor-positive/human epidermal growth factor receptor 2-negative (HR+/HER2-) metastatic breast cancer (mBC) in clinical trials and real-world studies. However, investigations of survival gains in broader HR+/HER2- mBC populations using epidemiological approaches are limited.
This retrospective study used SEER registry data to assess breast cancer-specific survival (BCSS) in patients diagnosed with HR+/HER2- de novo mBC from 2010 to 2019. Kaplan-Meier and Cox proportional hazards models were used to compare BCSS in patients diagnosed before (2010‒2013 with follow-up to 2014) and after (2015‒2018 with follow-up to 2019) the 2015 guideline recommendations for CDK4/6i use. A comparison was made to patients with HR+/HER2-positive (HER2+) de novo mBC, for which no major guideline changes occurred during 2015-2018.
Data from 11,467 women with HR+/HER2- mBC and 3260 women with HR+/HER2+ mBC were included. After baseline characteristic adjustment, patients with HR+/HER2- mBC diagnosed post-2015 (n = 6163), had an approximately 10% reduction in risk of BC-specific death compared with patients diagnosed pre-2015 (n = 5304; HR = 0.895, p < 0.0001). Conversely, no significant change was observed in HR+/HER2+ BCSS post-2015 (n = 1798) versus pre-2015 (n = 1462). Similar results were found in patients aged ≥ 65 years.
Using one of the largest US population-based longitudinal cancer databases, significant improvements in BCSS were noted in patients with HR+/HER2- mBC post-2015 versus pre-2015, potentially due to the introduction of CDK4/6i post-2015. No significant improvement in BCSS was observed in patients with HR+/HER2+ mBC post-2015 versus pre-2015, likely due to the availability of HER2-directed therapies in both time periods.
在临床试验和真实世界研究中,细胞周期蛋白依赖性激酶 4/6 抑制剂(CDK4/6i)已改善了激素受体阳性/人表皮生长因子受体 2 阴性(HR+/HER2-)转移性乳腺癌(mBC)患者的生存。然而,使用流行病学方法研究更广泛的 HR+/HER2-mBC 人群的生存获益的研究有限。
本回顾性研究使用 SEER 登记数据库,评估了 2010 年至 2019 年间诊断为 HR+/HER2-初发 mBC 的患者的乳腺癌特异性生存(BCSS)。Kaplan-Meier 和 Cox 比例风险模型用于比较 2015 年指南推荐 CDK4/6i 使用前后(2010-2013 年,随访至 2014 年;2015-2018 年,随访至 2019 年)诊断的患者的 BCSS。并与 HR+/HER2-阳性(HER2+)初发 mBC 患者进行了比较,在 2015-2018 年期间,该人群没有重大指南变化。
纳入了 11467 例 HR+/HER2-mBC 患者和 3260 例 HR+/HER2+ mBC 患者的数据。经过基线特征调整后,与 2015 年前诊断的患者(n=5304)相比,2015 年后诊断的 HR+/HER2-mBC 患者(n=6163)的 BC 特异性死亡风险降低了约 10%(HR=0.895,p<0.0001)。相反,2015 年后 HR+/HER2+BCSS 无显著变化(n=1798)与 2015 年前(n=1462)相比。在年龄≥65 岁的患者中也得到了类似的结果。
使用美国最大的基于人群的纵向癌症数据库之一,我们发现 2015 年后 HR+/HER2-mBC 患者的 BCSS 显著改善,与 2015 年前相比,这可能是由于 2015 年后 CDK4/6i 的应用。然而,在 2015 年后,HR+/HER2+ mBC 患者的 BCSS 与 2015 年前相比无显著改善,这可能是由于在这两个时间段都有曲妥珠单抗等 HER2 靶向治疗药物的应用。