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

机译:转移乳腺癌患者群体中环磷酰胺和甲氨蝶呤的低剂量度量化疗的勘探分析

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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.
机译:背景:低剂量衡量化疗(LDMC)越来越多地用于转移性乳腺癌(MBC)。在该回顾性分析中,我们研究了LDMC在MBC患者队列中的治疗效果和副作用。方法:在2009和2015年间施用具有口服环磷酰胺(CTX)和甲氨蝶呤(MTX)的LDMC时,包括MBC患者。在LDMC开始后,初级终点是疾病控制率(DCR)≥24周。次要终点是无进展的存活率(PFS)的持续时间,由于副作用而导致的停药率,以及关于亚组的DCR。结果:35名患者的回顾性数据可用于此分析。 31%的患者达到了DCR。中位数PFS是12周。由于不良事件,9%的患者停止了LDMC。 DCR在前2条线中为37%,进一步治疗中的25%。 22%的多重转移患者和35%≤2种不同的转移性位点DCR。 DCR是在33%的激素受体(HR) - 阳性患者中和27%的人类阴性患者中获得。结论:31%的DCR符合先前第二阶段研究的结果。 LDMC耐受良好。亚组分析无法识别LDMC更有效的组。

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