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1
Molecular features and clinical implications of the heterogeneity in Chinese patients with HER2-low breast cancer.中国 HER2 低表达乳腺癌患者异质性的分子特征及临床意义。
Nat Commun. 2023 Aug 22;14(1):5112. doi: 10.1038/s41467-023-40715-x.
2
Pathological complete response, category change, and prognostic significance of HER2-low breast cancer receiving neoadjuvant treatment: a multicenter analysis of 2489 cases.接受新辅助治疗的 HER2 低表达乳腺癌的病理完全缓解、分类改变及预后意义:一项 2489 例多中心分析。
Br J Cancer. 2023 Oct;129(8):1274-1283. doi: 10.1038/s41416-023-02403-x. Epub 2023 Aug 21.
3
Prognostic implications of HER2 changes after neoadjuvant chemotherapy in patients with HER2-zero and HER2-low breast cancer.新辅助化疗后 HER2 零表达和低表达乳腺癌患者 HER2 改变的预后意义。
Eur J Cancer. 2023 Sep;191:112956. doi: 10.1016/j.ejca.2023.112956. Epub 2023 Jun 24.
4
HER2-low breast cancer: evolution of HER2 expression from primary tumor to distant metastases.HER2 低表达乳腺癌:原发肿瘤至远处转移中 HER2 表达的演变。
BMC Cancer. 2023 Jul 13;23(1):656. doi: 10.1186/s12885-023-11134-4.
5
The dynamics of HER2-low expression during breast cancer progression.乳腺癌进展过程中 HER2 低表达的动态变化。
Breast Cancer Res Treat. 2023 Oct;201(3):437-446. doi: 10.1007/s10549-023-07020-z. Epub 2023 Jul 12.
6
Standardized Definitions for Efficacy End Points in Neoadjuvant Breast Cancer Clinical Trials: NeoSTEEP.新辅助乳腺癌临床试验疗效终点的标准化定义:NeoSTEEP。
J Clin Oncol. 2023 Sep 20;41(27):4433-4442. doi: 10.1200/JCO.23.00435. Epub 2023 Jul 11.
7
ESMO expert consensus statements (ECS) on the definition, diagnosis, and management of HER2-low breast cancer.ESMO 专家共识声明(ECS)关于 HER2 低表达乳腺癌的定义、诊断和管理。
Ann Oncol. 2023 Aug;34(8):645-659. doi: 10.1016/j.annonc.2023.05.008. Epub 2023 Jun 1.
8
Analysis of clinical features, genomic landscapes and survival outcomes in HER2-low breast cancer.HER2 低表达乳腺癌的临床特征、基因组图谱和生存结局分析。
J Transl Med. 2023 Jun 1;21(1):360. doi: 10.1186/s12967-023-04076-9.
9
Conversion of ER and HER2 Status After Neoadjuvant Therapy in Chinese Breast Cancer Patients.新辅助治疗后中国乳腺癌患者的 ER 和 HER2 状态的转换。
Clin Breast Cancer. 2023 Jun;23(4):436-446. doi: 10.1016/j.clbc.2023.03.002. Epub 2023 Mar 8.
10
Impact of residual disease biomarkers on the prognosis of HER2-positive breast cancer following neoadjuvant therapy.新辅助治疗后残留疾病生物标志物对 HER2 阳性乳腺癌预后的影响。
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新辅助化疗后HER-2阴性乳腺癌患者原发灶至残留病灶HER-2转化的演变及预后意义

Evolution and prognostic significance of HER-2 conversion from primary to residual disease in HER-2 negative patients with breast cancer after neoadjuvant chemotherapy.

作者信息

Chen Xi, Ji Lei, Qian Xiaoyan, Xiao Min, Li Qing, Li Qiao, Wang Jiayu, Fan Ying, Luo Yang, Lan Bo, Chen Shanshan, Ma Fei, Xu Binghe, Zhang Pin

机构信息

Department of Medical Oncology, National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College Beijing, China.

出版信息

Am J Cancer Res. 2024 Aug 25;14(8):3859-3872. doi: 10.62347/DGTD7801. eCollection 2024.

DOI:10.62347/DGTD7801
PMID:39267660
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11387869/
Abstract

This study aimed to analyze HER-2 zero or HER-2 low conversion in HER-2 negative patients after neoadjuvant chemotherapy (NAC) and evaluate its prognostic significance. HER-2 negative patients with breast cancer with residual disease after NAC and paired pre- and post-therapeutic HER-2 testing results were analyzed retrospectively. HER-2 low, defined as immunohistochemistry (IHC) scores of 1+ or 2+/in situ hybridization (ISH), were not amplified. HER-2 zero is defined as an IHC score of 0. A total of 571 patients were enrolled, including primary HER-2 zero (n=201, 35.2%) and HER-2 low (n=370, 64.8%). The overall HER-2 change rate was 32.4%. Multivariable logistic regression showed that patients with hormone receptor-positive status before NAC was significantly associated with the conversion of HER-2 zero to low (OR=3.436, < 0.0001). The median follow-up time was 50.0 months. In patients who are primary HER-2 zero, HER-2 zero to low was significantly associated with better disease-free survival (DFS) than constant HER-2 zero (HR=0.49, =0.01) after adjustment (4-year DFS 80.1% vs 55.7%, Log-rank =0.033). Subgroup analysis revealed that among patients who are primary HER-2 zero with hormone receptor-positive, HER-2 zero to low had a significantly better DFS than constant HER-2 zero (Log-rank =0.037). In contrast, patients with hormone receptor-negative status did not. In conclusion, almost one-third of patients who are HER-2 negative underwent HER-2 zero or HER-2 low conversion after NAC. HER-2 zero to low conversion was associated with better DFS in patients who are HER-2 zero. These results provide a valuable reference for the potential application of anti-HER-2 ADC in an adjuvant setting for patients with residual disease after NAC.

摘要

本研究旨在分析新辅助化疗(NAC)后HER-2阴性患者中HER-2零表达或HER-2低表达的转变情况,并评估其预后意义。对NAC后有残留病灶且有配对的治疗前和治疗后HER-2检测结果的HER-2阴性乳腺癌患者进行回顾性分析。HER-2低表达定义为免疫组织化学(IHC)评分为1+或2+/原位杂交(ISH)未扩增。HER-2零表达定义为IHC评分为0。共纳入571例患者,包括原发性HER-2零表达(n=201,35.2%)和HER-2低表达(n=370,64.8%)。HER-2的总体变化率为32.4%。多变量逻辑回归显示,NAC前激素受体阳性状态的患者与HER-2零表达向低表达的转变显著相关(OR=3.436,<0.0001)。中位随访时间为50.0个月。在原发性HER-2零表达的患者中,HER-2零表达向低表达转变者的无病生存期(DFS)显著优于持续HER-2零表达者(HR=0.49,=0.01),调整后(4年DFS 80.1%对55.7%,Log-rank=0.033)。亚组分析显示,在原发性HER-2零表达且激素受体阳性的患者中,HER-2零表达向低表达者的DFS显著优于持续HER-2零表达者(Log-rank=0.037)。相比之下,激素受体阴性的患者则不然。总之,近三分之一的HER-2阴性患者在NAC后发生了HER-2零表达或HER-2低表达的转变。HER-2零表达向低表达的转变与HER-2零表达患者更好的DFS相关。这些结果为抗HER-2 ADC在NAC后有残留病灶患者辅助治疗中的潜在应用提供了有价值的参考。