Breast Center Zurich, Zurich, Switzerland.
Faculty of Medicine, University of Basel, Basel, Switzerland.
Breast Cancer Res Treat. 2023 Sep;201(2):215-225. doi: 10.1007/s10549-023-06999-9. Epub 2023 Jun 25.
The aim of this study was to evaluate clinical practice heterogeneity in use of neoadjuvant systemic therapy (NST) for patients with clinically node-positive breast cancer in Europe.
The study was preplanned in the international multicenter phase-III OPBC-03/TAXIS trial (ClinicalTrials.gov Identifier: NCT03513614) to include the first 500 randomized patients with confirmed nodal disease at the time of surgery. The TAXIS study's pragmatic design allowed both the neoadjuvant and adjuvant setting according to the preferences of the local investigators who were encouraged to register eligible patients consecutively.
A total of 500 patients were included at 44 breast centers in six European countries from August 2018 to June 2022, 165 (33%) of whom underwent NST. Median age was 57 years (interquartile range [IQR], 48-69). Most patients were postmenopausal (68.4%) with grade 2 and 3 hormonal receptor-positive and human epidermal growth factor receptor 2-negative breast cancer with a median tumor size of 28 mm (IQR 20-40). The use of NST varied significantly across the countries (p < 0.001). Austria (55.2%) and Switzerland (35.8%) had the highest percentage of patients undergoing NST and Hungary (18.2%) the lowest. The administration of NST increased significantly over the years (OR 1.42; p < 0.001) and more than doubled from 20 to 46.7% between 2018 and 2022.
Substantial heterogeneity in the use of NST with HR+/HER2-breast cancer exists in Europe. While stringent guidelines are available for its use in triple-negative and HER2+ breast cancer, there is a need for the development of and adherence to well-defined recommendations for HR+/HER2-breast cancer.
本研究旨在评估欧洲临床淋巴结阳性乳腺癌患者新辅助全身治疗(NST)的临床实践异质性。
该研究是在国际多中心 III 期 OPBC-03/TAXIS 试验(ClinicalTrials.gov 标识符:NCT03513614)中预先计划的,纳入了在手术时确认有淋巴结疾病的前 500 名随机患者。TAXIS 研究的实用设计允许根据当地研究者的偏好进行新辅助和辅助治疗,鼓励他们连续注册符合条件的患者。
2018 年 8 月至 2022 年 6 月,来自六个欧洲国家的 44 个乳腺中心共纳入 500 例患者,其中 165 例(33%)接受了 NST。中位年龄为 57 岁(四分位距 [IQR],48-69)。大多数患者为绝经后(68.4%),激素受体阳性和人表皮生长因子受体 2 阴性,2 级和 3 级乳腺癌,肿瘤中位大小为 28mm(IQR 20-40)。各国之间 NST 的使用差异显著(p<0.001)。奥地利(55.2%)和瑞士(35.8%)接受 NST 的患者比例最高,匈牙利(18.2%)最低。NST 的应用在过去几年中显著增加(OR 1.42;p<0.001),从 2018 年的 20%到 2022 年的 46.7%,增加了一倍多。
欧洲 HR+/HER2-乳腺癌患者 NST 的使用存在显著异质性。尽管严格的指南可用于三阴性和 HER2+乳腺癌的 NST,但需要制定并遵守针对 HR+/HER2-乳腺癌的明确建议。