Li Chengxin, Yuan Qianqian, Deng Tong, Xu Gaoran, Hou Jinxuan, Zheng Lewei, Wu Gaosong
Department of Thyroid and Breast Surgery, Zhongnan Hospital Wuhan University, Wuhan, China.
Breast Cancer. 2023 Nov;30(6):965-975. doi: 10.1007/s12282-023-01487-w. Epub 2023 Jul 20.
HER2-low breast cancer (BC) is proposed to be a special population of patients with an immunohistochemistry (IHC) score of 1 + or 2 + and non-amplified in situ hybridization (ISH) results. The role and prognostic impact of HER2-low BC is still controversial. This meta-analysis aims to explore the prognostic difference between of HER2-low and HER2-zero characteristic in BC patients.
A meta-analysis was conducted using the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) guidelines and eligible studies were search in PubMed, Web of Science and EMBASE databases. Quality assessment of included studies were performed by Quality in Prognostic Studies (QUIPS) tool. Hazard ratios (HRs) and corresponding 95% confidence interval (CI) for overall survival (OS) and disease-free survival (DFS) were pooled in a meta-analysis. Furthermore, subgroup analysis, sensitivity analysis, and analysis for publication bias were conducted.
Eighteen studies comprising a total of 93,317 patients were included for meta-analysis. BC patients with HER2-low characteristic have longer OS (HRs 0.87, 95% CI 0.81-0.93, p < 0.0001) and DFS (HRs 0.82, 95% CI 0.73-0.93, p = 0.001) compared to those with HER2-zero characteristic. Subgroup analysis indicate that the source of heterogeneity may come from the hormone receptor (HR) status group. Although, the publication bias was detected, sensitivity analysis and the trim-and-fill method analysis demonstrated the stability and reliability of the results.
HER2-low BC patients have longer OS and DFS compared to HER2-zero BC patients, and its prognostic value is consistent among different HR status patients. Whether HER2-low breast cancer is an independent subtype of breast cancer is still a subject of ongoing research, and more studies are needed to fully understand the molecular and clinical features of this subtype.
人表皮生长因子受体2低表达型乳腺癌(BC)被认为是免疫组化(IHC)评分为1+或2+且原位杂交(ISH)结果未扩增的特殊患者群体。HER2低表达型BC的作用及预后影响仍存在争议。本荟萃分析旨在探讨BC患者中HER2低表达与HER2阴性特征之间的预后差异。
按照系统评价与荟萃分析的首选报告项目(PRISMA)指南进行荟萃分析,在PubMed、科学网和EMBASE数据库中检索符合条件的研究。采用预后研究质量(QUIPS)工具对纳入研究进行质量评估。在荟萃分析中汇总总生存期(OS)和无病生存期(DFS)的风险比(HR)及相应的95%置信区间(CI)。此外,还进行了亚组分析、敏感性分析和发表偏倚分析。
18项研究共纳入93317例患者进行荟萃分析。与HER2阴性特征的BC患者相比,HER2低表达特征的BC患者具有更长的OS(HR为0.87,95%CI为0.81 - 0.93,p < 0.0001)和DFS(HR为0.82,95%CI为0.73 - 0.93,p = 0.001)。亚组分析表明,异质性来源可能来自激素受体(HR)状态组。虽然检测到发表偏倚,但敏感性分析和裁剪填充法分析表明结果具有稳定性和可靠性。
与HER2阴性的BC患者相比,HER2低表达的BC患者具有更长的OS和DFS,并且其预后价值在不同HR状态的患者中是一致的。HER2低表达型乳腺癌是否为乳腺癌的独立亚型仍在研究中,需要更多研究来充分了解该亚型的分子和临床特征。