Suppr超能文献

在新辅助试验 GeparQuinto 和 GeparSixto 中接受治疗的乳腺癌患者,其中枢神经系统转移作为转移性疾病的首发部位。

Development of central nervous system metastases as a first site of metastatic disease in breast cancer patients treated in the neoadjuvant trials GeparQuinto and GeparSixto.

机构信息

Department of Gynecology, University Medical Center Hamburg-Eppendorf, Martinistrasse 52, 20246, Hamburg, Germany.

Department of Gynecology and Obstetrics, University Hospital Erlangen, Comprehensive Cancer Center Erlangen-EMN, Friedrich-Alexander University Erlangen-Nuremberg, Erlangen, Germany.

出版信息

Breast Cancer Res. 2019 May 10;21(1):60. doi: 10.1186/s13058-019-1144-x.

Abstract

BACKGROUND

The incidence of central nervous system (CNS) metastases in breast cancer patients is rising and has become a major clinical challenge. Only few data are published concerning risk factors for the development of CNS metastases as a first site of metastatic disease in breast cancer patients. Moreover, the incidence of CNS metastases after modern neoadjuvant treatment is not clear.

METHODS

We analyzed clinical factors associated with the occurrence of CNS metastases as the first site of metastatic disease in breast cancer patients after neoadjuvant treatment in the trials GeparQuinto and GeparSixto (n = 3160) where patients received targeted treatment in addition to taxane and anthracycline-based chemotherapy.

RESULTS

After a median follow-up of 61 months, 108 (3%) of a total of 3160 patients developed CNS metastases as the first site of recurrence and 411 (13%) patients had metastatic disease outside the CNS. Thirty-six patients (1%) developed both CNS metastases and other distant metastases as the first site of metastatic disease. Regarding subtypes of the primary tumor, 1% of luminal A-like (11/954), 2% of luminal B-like (7/381), 4% of HER2-positive (34/809), and 6% of triple-negative patients (56/1008) developed CNS metastases as the first site of metastatic disease. In multivariate analysis, risk factors for the development of CNS metastases were larger tumor size (cT3-4; HR 1.63, 95% CI 1.08-2.46, p = 0.021), node-positive disease (HR 2.57, 95% CI 1.64-4.04, p < 0.001), no pCR after neoadjuvant chemotherapy (HR 2.29, 95% CI 1.32-3.97, p = 0.003), and HER2-positive (HR 3.80, 95% CI 1.89-7.64, p < 0.001) or triple-negative subtype (HR 6.38, 95% CI 3.28-12.44, p < 0.001).

CONCLUSIONS

Especially patients with HER2-positive and triple-negative tumors are at risk of developing CNS metastases despite effective systemic treatment. A better understanding of the underlying mechanisms is required in order to develop potential preventive strategies.

摘要

背景

乳腺癌患者中枢神经系统(CNS)转移的发生率正在上升,已成为主要的临床挑战。仅有少数数据涉及乳腺癌患者作为转移性疾病的首发部位发生 CNS 转移的危险因素。此外,接受现代新辅助治疗后的 CNS 转移发生率尚不清楚。

方法

我们分析了在 GeparQuinto 和 GeparSixto 试验(n=3160)中,接受紫杉烷和蒽环类化疗联合靶向治疗的新辅助治疗后乳腺癌患者中 CNS 转移作为首发转移部位的临床相关因素。

结果

中位随访 61 个月后,3160 例患者中有 108 例(3%)发生 CNS 转移作为首发转移部位,411 例(13%)患者出现 CNS 外转移性疾病。36 例(1%)患者同时出现 CNS 转移和其他远处转移作为首发转移部位。根据原发肿瘤亚型,1%的 luminal A 样(11/954)、2%的 luminal B 样(7/381)、4%的 HER2 阳性(34/809)和 6%的三阴性患者(56/1008)发生 CNS 转移作为首发转移部位。多变量分析显示,发生 CNS 转移的危险因素包括较大的肿瘤大小(cT3-4;HR 1.63,95%CI 1.08-2.46,p=0.021)、淋巴结阳性疾病(HR 2.57,95%CI 1.64-4.04,p<0.001)、新辅助化疗后无 pCR(HR 2.29,95%CI 1.32-3.97,p=0.003)和 HER2 阳性(HR 3.80,95%CI 1.89-7.64,p<0.001)或三阴性亚型(HR 6.38,95%CI 3.28-12.44,p<0.001)。

结论

尽管进行了有效的全身治疗,但 HER2 阳性和三阴性肿瘤的患者尤其有发生 CNS 转移的风险。需要更好地了解潜在的发病机制,以便制定潜在的预防策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0048/6509843/d389dc4708ab/13058_2019_1144_Fig1_HTML.jpg

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