Hacettepe University Cancer Institute, Ankara, Turkey.
Health Sciences University, Elazig City Hospital, Elazig, Turkey.
Breast Cancer Res Treat. 2024 Apr;204(3):443-452. doi: 10.1007/s10549-023-07226-1. Epub 2024 Jan 19.
The cyclin-dependent kinase (CDK) 4/6 inhibitors significantly altered the treatment landscape of hormone-positive (HR+), HER2- metastatic breast cancer (MBC). However, biomarkers predicting long-term benefit and early progression are yet to be defined. Several studies suggested the possibility of diminished efficacy in patients with HER2-low disease. Therefore, we conducted a systematic review and meta-analysis to evaluate the association between low-level HER2 expression and efficacy outcomes (PFS, OS, ORR) with CDK 4/6 inhibitors.
The Pubmed, Web of Science, and Scopus databases were used to systematically filter the published studies from inception to 08 August 2023 for this systemic review. Studies including MBC patients treated with CDK 4/6 inhibitors and reported survival outcomes according to HER2 expression were included. We performed the meta-analyses with the generic inverse-variance method with a fixed-effects model and used HRs with 95% two-sided CIs as the principal summary measure.
Nine studies encompassing 2705 patients were included in the analyses. In the pooled analysis of nine studies, the risk of progression and/or death was higher in patients with HER2-low tumors compared to HER2-zero (HR: 1.22, 95% CI 1.10-1.35, p < 0.001). In the pooled analysis of five studies, although the median follow-up was short, the risk of death was higher in the HER2-low group compared to the HER2-zero group (HR: 1.22, 95% CI 1.04-1.44, p = 0.010).
The available evidence demonstrates a significantly higher risk of progression or death with CDK 4/6 inhibitors in HER2-low tumors. Further research is needed to improve outcomes in patients with HR+-HER2-low tumors.
细胞周期蛋白依赖性激酶(CDK)4/6 抑制剂显著改变了激素阳性(HR+)、HER2-转移性乳腺癌(MBC)的治疗格局。然而,预测长期获益和早期进展的生物标志物尚未确定。一些研究表明,HER2 低表达疾病患者的疗效可能降低。因此,我们进行了一项系统评价和荟萃分析,以评估 CDK 4/6 抑制剂与低水平 HER2 表达与疗效结局(PFS、OS、ORR)之间的关系。
我们使用 Pubmed、Web of Science 和 Scopus 数据库,从成立到 2023 年 8 月 8 日,系统地筛选了已发表的研究,以进行这项系统评价。纳入的研究包括接受 CDK 4/6 抑制剂治疗并根据 HER2 表达报告生存结局的 MBC 患者。我们使用固定效应模型的通用逆方差法进行荟萃分析,并使用 HRs 和 95%双侧 CIs 作为主要汇总指标。
共有 9 项研究,包含 2705 例患者,纳入了分析。在 9 项研究的荟萃分析中,与 HER2-零组相比,HER2-低肿瘤患者的进展和/或死亡风险更高(HR:1.22,95%CI 1.10-1.35,p<0.001)。在 5 项研究的荟萃分析中,尽管中位随访时间较短,但与 HER2-零组相比,HER2-低组的死亡风险更高(HR:1.22,95%CI 1.04-1.44,p=0.010)。
现有证据表明,HER2-低肿瘤患者使用 CDK 4/6 抑制剂治疗的进展或死亡风险显著增加。需要进一步研究以改善 HR+-HER2-低肿瘤患者的结局。