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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:转移性乳腺癌患者队列中环磷酰胺和甲氨蝶呤小剂量节律化疗的探索性分析

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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:背景技术低剂量节律化疗(LDMC)越来越多地用于转移性乳腺癌(MBC)。在这项回顾性分析中,我们检查了LDMC在一组MBC患者中的治疗效果和副作用。方法在2009年至2015年期间,给予口服环磷酰胺(CTX)和甲氨蝶呤(MTX)的LDMC并入MBC患者。主要终点是疾病控制率(DCR)≥LDMC开始后24周。次要终点是无进展生存期(PFS),由于副作用导致的停药率以及关于亚组的DCR。结果35例患者的回顾性数据可用于该分析。 31%的患者达到了DCR。中位PFS为12周。 9%的患者因不良事件而停药。前两个疗程的DCR为37%,其他疗程的DCR为25%。 22%的多发转移患者和35%≤2个不同转移部位的患者实现了DCR。在33%的激素受体(HR)阳性患者和27%的HR阴性患者中实现了DCR。结论31%的DCR与先前II期研究的结果一致。 LDMC的耐受性良好。子组分析无法确定LDMC更有效的组。

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