美国引入 CDK4/6 抑制剂前后 HR+ 转移性乳腺癌患者的生存趋势:对 HER2- 和 HER2+ 转移性乳腺癌患者的 SEER 登记分析。

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
ACS Applied Electronic Materials Pub Date : 2024-11-01 Epub Date: 2024-08-23 DOI:10.1007/s10549-024-07469-6
Adam Brufsky, Marilyn L Kwan, Rickard Sandin, Stella Stergiopoulos, Siddharth Karanth, Ashley S Cha-Silva, Doris Makari, Ravi K Goyal
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引用次数: 0

摘要

目的:在临床试验和实际研究中,细胞周期蛋白依赖性激酶4/6抑制剂(CDK4/6i)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)患者的生存率。然而,利用流行病学方法对更广泛的HR+/HER2- mBC人群的生存率提高情况进行的调查还很有限:这项回顾性研究利用SEER登记数据评估了2010年至2019年确诊为HR+/HER2-新发mBC患者的乳腺癌特异性生存率(BCSS)。研究使用卡普兰-梅耶尔模型和考克斯比例危险模型比较了2015年指南建议使用CDK4/6i之前(2010-2013年,随访至2014年)和之后(2015-2018年,随访至2019年)确诊患者的BCSS。与HR+/HER2阳性(HER2+)新发型mBC患者进行了比较,2015-2018年期间该指南未发生重大变化:纳入了11467名HR+/HER2- mBC女性患者和3260名HR+/HER2+ mBC女性患者的数据。经过基线特征调整后,2015年后确诊的HR+/HER2- mBC患者(n = 6163)与2015年之前确诊的患者(n = 5304; HR = 0.895, p 结论:与2015年之前确诊的患者相比,HR+/HER2- mBC患者的BC特异性死亡风险降低了约10%:利用美国最大的人口纵向癌症数据库之一,发现2015年后与2015年之前相比,HR+/HER2- mBC患者的BCSS显著改善,这可能是由于2015年后引入了CDK4/6i。2015年后与2015年之前相比,HR+/HER2+ mBC患者的BCSS没有明显改善,这可能是由于这两个时期都有HER2导向疗法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Trends in HR+ metastatic breast cancer survival before and after CDK4/6 inhibitor introduction in the United States: a SEER registry analysis of patients with HER2- and HER2+ metastatic breast cancer.

Trends in HR+ metastatic breast cancer survival before and after CDK4/6 inhibitor introduction in the United States: a SEER registry analysis of patients with HER2- and HER2+ metastatic breast cancer.

Purpose: 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.

Methods: 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.

Results: 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.

Conclusion: 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.

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CiteScore
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