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乳腺癌患者 Ki67 的组织学特征及其预后评估:一项单中心、横断面研究的结果。

Histological Aspects and Quantitative Assessment of Ki67 as Prognostic Factors in Breast Cancer Patients: Result from a Single-Center, Cross Sectional Study.

机构信息

Faculty of Medicine, Faculty of Midwifery and Nursing, Carol Davila University of Medicine and Pharmacy, 020021 Bucharest, Romania.

Clinic of Oncology, Elias Universitary Emergency Hospital, 011461 Bucharest, Romania.

出版信息

Medicina (Kaunas). 2020 Nov 9;56(11):600. doi: 10.3390/medicina56110600.

Abstract

Our aim is to explore the relationship between the levels of protein encoded by Ki67 and the histopathological aspects regarding the overall survival and progression-free survival in a single university center. A secondary objective was to examine other factors that can influence these endpoints. New approaches to the prognostic assessment of breast cancer have come from molecular profiling studies. Ki67 is a nuclear protein associated with cell proliferation. Together with the histological type and tumor grade, it is used to appreciate the aggressiveness of the breast tumors. We conducted a retrospective single-institution study, at Elias University Emergency Hospital, Bucharest, Romania, in which we enrolled women with stage I to III breast cancer. The protocol was amended to include the immunohistochemistry determination of Ki67 and the histological aspects. The methodology consisted in using a Kaplan-Meier analysis for the entire sample and restricted mean survival time up to 36 months. Both lower Ki67 and low tumor grade are associated with better prognosis in terms of overall survival (OS) and progression-free survival (PFS) for our patients' cohort. In our group, the histological type did not impact the time to progression or survival. Both overall survival and progression-free survival may be influenced by the higher value of Ki67 and less differentiated tumors. Further studies are needed in order to establish if the histologic type may impact breast cancer prognostic, probably together with other histologic and molecular markers.

摘要

我们的目的是在单一大学中心探索 Ki67 编码蛋白水平与总生存和无进展生存的组织病理学方面之间的关系。次要目标是检查其他可能影响这些终点的因素。乳腺癌预后评估的新方法来自分子谱研究。Ki67 是一种与细胞增殖相关的核蛋白。与组织学类型和肿瘤分级一起,它用于评估乳腺癌的侵袭性。

我们在罗马尼亚布加勒斯特 Elias 大学急诊医院进行了一项回顾性单机构研究,纳入了 I 期至 III 期乳腺癌女性。方案进行了修订,包括 Ki67 的免疫组织化学测定和组织学方面。方法包括对整个样本进行 Kaplan-Meier 分析和 36 个月的受限平均生存时间。

对于我们患者队列的总生存(OS)和无进展生存(PFS),较低的 Ki67 和低肿瘤分级都与更好的预后相关。在我们的组中,组织学类型并不影响进展时间或生存。Ki67 值较高和肿瘤分化程度较低均可影响总生存和无进展生存。为了确定组织学类型是否可能影响乳腺癌的预后,可能需要进一步研究,可能需要结合其他组织学和分子标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8664/7698204/2b01e5cff05b/medicina-56-00600-g001.jpg

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