Prognostic outcomes in advanced breast cancer: the metastasis-free interval is important

被引:19
作者
Shen, Tiansheng [1 ]
Gao, Cheng [2 ]
Zhang, Kui [2 ]
Siegal, Gene P. [1 ]
Wei, Shi [1 ]
机构
[1] Univ Alabama Birmingham, Dept Pathol, NP 3542,619 19th St S, Birmingham, AL 35249 USA
[2] Michigan Technol Univ, Dept Math Sci, Houghton, MI 49931 USA
关键词
Breast cancer; Metastasis-free interval; Overall survival; Metastasis; Prognosis; NOVO STAGE IV; DE-NOVO; SURVIVAL; WOMEN; EVOLUTION; SUBTYPE; DISEASE;
D O I
10.1016/j.humpath.2017.10.002
中图分类号
R36 [病理学];
学科分类号
100104 ;
摘要
Metastatic breast cancer is a heterogeneous disease with a diverse clinical course. There have been limited studies regarding prognostic outcomes in patients with de novo metastatic breast cancer versus those with metastatic recurrence, with controversial observations. In this study, we sought to examine the difference in survival outcomes among patients with advanced breast cancer stratified based on metastasis-free interval (MFI) and to further explore the role of systemic therapy in these patient groups. Of 569 consecutive patients with stage IV breast cancer between 1998 and 2013, 201 had de novo metastatic disease (metastasis at diagnosis) and 368 developed metastatic recurrence, including 168 with an MFI <= 24 months and 200 with an MFI > 24 months. In the 492 patients who received systemic therapy, de novo metastasis was an independent favorable prognostic factor for overall survival after metastasis when compared with metastatic recurrence irrespective of MFI. Compared with the patients with metastatic recurrence with an MFI <= 24 months, those with an MFI > 24 months had a superior survival outcome, although it did not reach statistical significance by multivariate analysis. In contrast, de novo metastatic breast cancer was associated with a worse prognosis when compared with recurring metastasis in the patients who did not receive systemic treatment. These findings provide more insight into the natural history of advanced breast cancer, thus necessitating further investigation into the molecular mechanism of drug resistance. (C) 2017 Elsevier Inc. All rights reserved.
引用
收藏
页码:70 / 76
页数:7
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