Explorative Analysis of Low-Dose Metronomic Chemotherapy with Cyclophosphamide and Methotrexate in a Cohort of Metastatic Breast Cancer Patients

被引:15
作者
Krajnak, Slavomir [1 ]
Battista, Marco [1 ]
Brenner, Walburgis [1 ]
Almstedt, Katrin [1 ]
Elger, Tania [1 ]
Heimes, Anne-Sophie [1 ]
Hasenburg, Annette [1 ]
Schmidt, Marcus [1 ]
机构
[1] Univ Med Ctr Mainz, Dept Gynecol & Obstet, Langenbeckstr 1, D-55131 Mainz, Germany
关键词
Adverse events; Breast cancer; Metastasized; Chemotherapy; Metronomic chemotherapy; Cyclophosphamide; Methotrexate; ENDOTHELIAL GROWTH-FACTOR; ORAL CYCLOPHOSPHAMIDE; ANTITUMOR-ACTIVITY; THERAPY; VINORELBINE; RESISTANCE; CELLS; TRIAL; BEVACIZUMAB; PLUS;
D O I
10.1159/000487629
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Background: Low-dose metronomic chemotherapy (LDMC) is increasingly used in metastatic breast cancer (MBC). In this retrospective analysis, we examined the therapeutic effects and side effects of LDMC in a cohort of MBC patients. Methods: Patients with MBC were included when LDMC with oral cyclophosphamide (CTX) and methotrexate (MTX) was administered between 2009 and 2015. The primary endpoint was disease control rate (DCR) >= 24 weeks after the start of LDMC. Secondary endpoints were duration of progression-free survival (PFS), rates of discontinuation due to side effects, and DCR with regard to subgroups. Results: Retrospective data of 35 patients were available for this analysis. 31% patients achieved DCR. The median PFS was 12 weeks. 9% of patients discontinued LDMC due to adverse events. DCR was 37% in the first 2 lines and 25% in further lines of therapy. 22% of patients with multiple metastases and 35% with <= 2 different metastatic sites achieved DCR. DCR was achieved in 33% of hormone receptor(HR)-positive patients and 27% of HR-negative patients. Conclusion: The DCR of 31% is in line with the results of previous phase II studies. LDMC was well tolerated. Subgroup analysis was not able to identify a group in which LDMC was more efficient. (C) 2018 S. Karger GmbH, Freiburg
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收藏
页码:272 / 276
页数:5
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