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乳腺癌患者的治疗与结局:来自 EUSOMA 乳腺中心网络的横断面研究

英文原题:Treatment and outcomes in breast cancer patients: A cross section study from the EUSOMA breast centre network.

查看英文原题

Treatment and outcomes in breast cancer patients: A cross section study from the EUSOMA breast centre network.

PubMed 2023/11/14(内容时间) Eur J Cancer Q1 · IF 7.9(JCR 2025)

分数与星级只用于站内排序 —— 不代表疗效、安全性或个人适用性。

研究概要

目前的结果显示,庞大的患者数据库提供了一条信息流,可用于减少临床实践中的不确定性。数据库参数需要动态更新以进行结果监测。应加入分子预后因素、基因表达特征、TIL(肿瘤浸润淋巴细胞)和循环肿瘤 DNA。

研究思路结论见上方概要

本研究旨在描述乳腺癌患者的肿瘤特征和治疗情况,并评估远处转移风险与生物学特征、疾病分期及治疗之间的关系。

数据来自EUSOMA数据库中的81,882例患者(诊断时疾病分期为0-IV期;中位年龄61岁;范围20-100岁)。所有患者均在2016年1月至2021年12月期间,于13个欧洲国家53个通过EUSOMA认证流程的乳腺中心接受治疗。病例被分类为HR+/HER2-、HR+/HER2+、HR-/HER2+或HR-/HER2-,并据此进行数据分析。

对38,119例有是否发生远处转移信息的病例子集进行了单变量和多变量分析。潜在决定因素包括亚组类型、Ki67值、疾病分期、辅助全身治疗和术后放疗。在多变量分析中,HR-/HER2+和HR-/HER2-亚组与HR+/HER2-相比,远处转移风险更高。Ki67 > 20 %和晚期疾病也具有高风险。放疗成为远处转移的保护因素。

展开英文摘要原文

Data were analysed from 81,882 patients in the EUSOMA database (disease stages at diagnosis 0-IV; median age 61 years; range 20-100 years). All patients were treated between January 2016 and December 2021 in 53 Breast Centres within the EUSOMA certification process in 13 European countries. Cases were classified as HR+ /HER2-, HR+ /HER2 + , HR-/HER2 + or HR-/HER2- and data were analysed accordingly.

Univariable and multivariable analyses for distant metastases were conducted on a subset of 38,119 cases with information on whether or not they had developed them. Potential determinants included sub-group type, Ki67 value, disease stage, adjuvant systemic therapies and post-operative radiation therapy. In multivariable analysis, the HR-/HER2 + and HR-/HER2- sub-groups were associated with a higher risk of distant metastases than HR+ /HER2-. Ki67 > 20 % and advanced stage disease also carried a high risk. Radiation therapy emerged as a protective factor against distant metastases.

Present results show a large patient database offers an information stream that can be applied to reduce uncertainties in clinical practice. Database parameters need to be updated dynamically for outcome monitoring. Molecular prognostic factors, gene-expression signatures, tumour-infiltrating lymphocytes and circulating tumoral DNA should be added.

论文信息

作者
Aristei C、Tomatis M、Antonio Ponti、Marotti L、Cardoso MJ、Cheung KL、Curigliano G、De Vries J
单位
Radiation Oncology Section, Department of Medicine and Surgery, University of Perugia and Perugia General Hospital Sant'Andrea delle Fratte Perugia Italy. Electronic address: cynthia.aristei@unipg.it.Italy
期刊
European journal of cancer (Oxford, England : 1990)2024 Jan
原文标识
PubMed 37995597 · DOI 10.1016/j.ejca.2023.113438