Suppr超能文献

Ki-67指数值和孕激素受体状态可预测雌激素受体阳性且人表皮生长因子受体2阴性的淋巴结阴性乳腺癌患者的预后及合适的治疗方案。

Ki-67 index value and progesterone receptor status can predict prognosis and suitable treatment in node-negative breast cancer patients with estrogen receptor-positive and HER2-negative tumors.

作者信息

Arima Nobuyuki, Nishimura Reiki, Osako Tomofumi, Okumura Yasuhiro, Nakano Masahiro, Fujisue Mamiko, Nishiyama Yasuyuki, Toyozumi Yasuo

机构信息

Department of Pathology, Kumamoto Shinto General Hospital, Kumamoto 862-8655, Japan.

Department of Breast Oncology, Kumamoto Shinto General Hospital, Kumamoto 862-8655, Japan.

出版信息

Oncol Lett. 2019 Jan;17(1):616-622. doi: 10.3892/ol.2018.9633. Epub 2018 Oct 29.

Abstract

Gene profiling has identified at least 4 breast cancer subtypes, including Luminal A, Luminal B, HER2-enriched and basal-like, and immunohistochemistry is used as a guide to determine these subtypes. In the present study, patients with ER-positive, HER2-negative and negative nodes were classified into 4 groups according to the PgR and the Ki-67 status and were retrospectively examined. The analysis was based on the clinicopathological findings, and includes the recurrence score (RS) and disease-free survival (DFS) rates. Patients with invasive breast cancer (n=1866) were classified as LA (high PgR/low Ki-67), LB-1 (high PgR/high Ki-67), LB-2 (low PgR/high Ki-67), and LB-3 (low PgR/low Ki-67). In addition, 41 of the cases underwent a 21-gene expression assay. The data revealed that T1 tumors were more prevalent in the LA group and rare in the LB-2 group. Furthermore, nuclear grade 3 and p53 overexpression was revealed to be significantly correlated with LB-2. In terms of prognosis, LA had a significantly more favorable DFS; however, no differences were observed in the LB-3 group. LB-2 had a significantly worse DFS in all cases, and in the cases administered with endocrine therapy alone. Chemotherapy in combination with endocrine therapy was administered to cases with a higher risk of recurrence. In the LB-2 group, there was no difference in the DFS rates between the cases with endocrine therapy and chemo-endocrine therapy. These findings suggest that chemotherapy could improve the DFS in the LB-2 group. In addition, the majority of cases with LA, LB-3 and LB-1 had a RS of ≤25 and the majority of the LB-2 cases had a RS of >25. The patients with LA and LB-3 had a favorable DFS even in the group that received endocrine therapy alone. LB-2 was significantly correlated with a higher degree of malignancy and benefited from chemotherapy. These data suggest that the PgR and the Ki-67 status are effective in predicting prognosis, and for deciding on the most effective treatment strategy in patients with breast cancer.

摘要

基因谱分析已确定至少4种乳腺癌亚型,包括腔面A型、腔面B型、HER2富集型和基底样型,免疫组化被用作确定这些亚型的指导方法。在本研究中,雌激素受体(ER)阳性、HER2阴性且无淋巴结转移的患者根据孕激素受体(PgR)和Ki-67状态分为4组,并进行回顾性研究。分析基于临床病理结果,包括复发评分(RS)和无病生存率(DFS)。浸润性乳腺癌患者(n = 1866)被分为LA(高PgR/低Ki-67)、LB-1(高PgR/高Ki-67)、LB-2(低PgR/高Ki-67)和LB-3(低PgR/低Ki-67)。此外,41例患者进行了21基因表达检测。数据显示,T1期肿瘤在LA组中更为常见,在LB-2组中罕见。此外,核分级3级和p53过表达与LB-2显著相关。在预后方面,LA组的DFS明显更好;然而,LB-3组未观察到差异。LB-2组在所有病例以及仅接受内分泌治疗的病例中DFS明显更差。复发风险较高的病例接受化疗联合内分泌治疗。在LB-2组中,内分泌治疗病例和化疗-内分泌治疗病例的DFS率没有差异。这些发现表明化疗可以改善LB-2组的DFS。此外,大多数LA、LB-3和LB-1病例的RS≤25,大多数LB-2病例的RS>25。LA和LB-3患者即使在仅接受内分泌治疗的组中DFS也较好。LB-2与更高程度的恶性肿瘤显著相关,并且从化疗中获益。这些数据表明PgR和Ki-67状态可有效预测预后,并有助于决定乳腺癌患者最有效的治疗策略。

相似文献

8
Is triple negative a prognostic factor in breast cancer?三阴性是乳腺癌的一个预后因素吗?
Breast Cancer. 2008;15(4):303-8. doi: 10.1007/s12282-008-0042-3. Epub 2008 Mar 29.
10
Prognostic Factors for Luminal B-like Breast Cancer.腔面 B 型乳腺癌的预后因素。
Curr Med Sci. 2019 Jun;39(3):396-402. doi: 10.1007/s11596-019-2049-8. Epub 2019 Jun 17.

引用本文的文献

4
The impact of the HER2-low status on conditional survival in patients with breast cancer.HER2低表达状态对乳腺癌患者条件生存的影响。
Ther Adv Med Oncol. 2024 Jan 19;16:17588359231225039. doi: 10.1177/17588359231225039. eCollection 2024.

本文引用的文献

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验