Incidence of Metastasis in the Central Nervous System in Advanced Breast Cancer Treated With CDK 4/6 Inhibitors: A Multicenter, Retrospective Study

IF 10.7 Q1 MEDICINE, RESEARCH & EXPERIMENTAL
MedComm Pub Date : 2025-05-24 DOI:10.1002/mco2.70221
Yan-Ling Wen, Xi-Wen Bi, Xue-Wen Zhang, Si-Fen Wang, Chang Jiang, Li Wang, Yong-Yi Zhong, Yuan-Yuan Huang, Jian-Li Zhao, Qian-Jun Chen, Cong Xue, Zhong-Yu Yuan
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Abstract

Central nervous system (CNS) metastasis remains a major cause of mortality in advanced breast cancer (ABC). While cyclin-dependent kinase 4/6 inhibitors (CDKIs) combined with endocrine therapy (ET) delay resistance in hormone receptor (HR)-positive and human epidermal growth factor receptor 2 (HER2)-negative ABC, their impact on CNS metastasis development has not been fully elucidated. This retrospective study analyzed 435 ABC patients without baseline CNS metastases who received first-line ET with or without CDKIs across three Chinese hospitals (August 2018–July 2022). Primary end points included CNS as the first metastatic site, CNS metastasis-free survival (CNSM-FS), and CNS metastasis incidence over time. Secondary end points were progression-free survival (PFS) and overall survival (OS). The results indicated that the addition of CDKIs to ET significantly reduced the incidence of CNS as the first site of metastasis (3.7% vs. 9.5% with ET alone; p = 0.0015) and extended CNSM-FS (71.6 months vs. 63.6 months, respectively; hazard ratio [HR], 0.53; 95% CI, 0.31–0.92). Overall, CNS metastasis incidence was lower with ET + CDKIs (7.9% vs. 15.5%, p = 0.014), and improvements were observed in both PFS and OS. These findings suggest that ET + CDKIs as first-line therapy in ABC may reduce CNS metastasis risk and extend CNSM-FS, offering a potential strategy for preventing CNS metastases.

cdk4 /6抑制剂治疗晚期乳腺癌中枢神经系统转移的发生率:一项多中心回顾性研究
中枢神经系统(CNS)转移仍然是晚期乳腺癌(ABC)死亡的主要原因。虽然细胞周期蛋白依赖性激酶4/6抑制剂(CDKIs)联合内分泌治疗(ET)延缓了激素受体(HR)阳性和人表皮生长因子受体2 (HER2)阴性ABC的耐药,但它们对中枢神经系统转移发展的影响尚未完全阐明。这项回顾性研究分析了中国三家医院(2018年8月至2022年7月)435例基线无中枢神经系统转移的ABC患者,这些患者接受了一线ET治疗,有或没有CDKIs。主要终点包括中枢神经系统作为第一转移部位、中枢神经系统无转移生存期(CNSM-FS)和中枢神经系统随时间的转移发生率。次要终点为无进展生存期(PFS)和总生存期(OS)。结果表明,在ET中添加CDKIs可显著降低CNS作为第一转移部位的发生率(3.7% vs.单独使用ET的9.5%;p = 0.0015)和延长的CNSM-FS(分别为71.6个月对63.6个月;风险比[HR], 0.53;95% ci, 0.31-0.92)。总的来说,ET + CDKIs的中枢神经系统转移发生率较低(7.9% vs. 15.5%, p = 0.014), PFS和OS的转移发生率均有改善。这些发现表明,ET + CDKIs作为ABC的一线治疗可能降低中枢神经系统转移风险,延长CNSM-FS,为预防中枢神经系统转移提供了一种潜在的策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
6.70
自引率
0.00%
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审稿时长
10 weeks
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