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首页> 外文期刊>Tumour biology : >Apatinib for metastatic breast cancer in non-clinical trial setting: Satisfying efficacy regardless of previous anti-angiogenic treatment
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Apatinib for metastatic breast cancer in non-clinical trial setting: Satisfying efficacy regardless of previous anti-angiogenic treatment

机译:阿帕替尼用于非临床试验环境中的转移性乳腺癌:无论以前是否进行抗血管生成治疗,其疗效均令人满意

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摘要

Apatinib is a novel tyrosine kinase inhibitor targeting vascular endothelial growth factor receptor 2. This study aimed to evaluate the efficacy and safety of apatinib in metastatic breast cancer (MBC) under non-clinical trial setting, and to study the impact of previous antiangiogenic treatment to the efficacy of apatinib. 52 MBC patients treated with apatinib under non-clinical trial setting in Fudan University Shanghai Cancer Center between January 1st 2015 and October 1st 2016 were included. All patients were included in time-to-treatment failure (TTF) analysis, while 45 patients were enrolled for progression-free survival (PFS) and overall survival (OS) analysis because 7 of the patients with treatment discontinuation due to intolerable toxicities had too short time for efficacy assessment. Impact of previous exposure to antiangiogenic treatment and other factors to patients’ survival were analyzed by Log-rank analysis and Cox multivariate analysis. The median PFS, median OS, and median TTF were 4.90 (95% confidence interval [CI] 3.44 – 6.36), 10.3 (unable to calculate 95% CI), and 3.93 (95% CI 1.96 – 5.90) months, respectively. Previous treatment of bevacizumab did not affect the efficacy of apatinib. Previous exposure to anthracycline, age of 60 years or older and palmar-plantar erythrodysesthesia syndrome were independent predictors for prolonged PFS. Discontinuation of treatment was more common in age group of 60 years or older than that in younger group, although the difference was not significant. Although toxicities were generally managable, a previously unrecorded grade 3~4 adverse event of dyspnea has been observed. This study confirmed the encouraging efficacy and manageable safety of apatinib on pretreated MBC patients in non-clinical trial setting. For the first time to our knowledge, this study found that previous treatment of bevacizumab did not affect the efficacy of apatinib, and reported an undocumented severe adverse effect of dyspnea.
机译:Apatinib是靶向血管内皮生长因子受体2的新型酪氨酸激酶抑制剂。该研究旨在评估apatinib在非临床试验条件下对转移性乳腺癌(MBC)的疗效和安全性,并研究先前的抗血管生成治疗对阿帕替尼的疗效。纳入2015年1月1日至2016年10月1日在复旦大学附属上海肿瘤中心接受非临床试验设置的52例接受阿帕替尼治疗的MBC患者。所有患者均纳入治疗失败时间(TTF)分析,而45名患者入选了无进展生存期(PFS)和总体生存期(OS)分析,因为其中7名因无法忍受的毒性而中止治疗的患者也是如此疗效评估时间短。通过Log-rank分析和Cox多变量分析分析了先前接受抗血管生成治疗的影响以及其他因素对患者生存的影响。中位PFS,中位OS​​和中位TTF分别为4.90(95%置信区间[CI] 3.44 – 6.36),10.3(无法计算95%CI)和3.93(95%CI 1.96 – 5.90)个月。贝伐单抗的先前治疗未影响阿帕替尼的疗效。先前曾接触过蒽环类药物,年龄在60岁或60岁以上以及掌-红斑感觉异常是长期PFS的独立预测因素。在60岁或60岁以上的年龄组中,终止治疗比在年轻组中更常见,尽管差异不显着。尽管毒性通常是可控制的,但已观察到以前未记录的呼吸困难的3〜4级不良事件。这项研究证实了在非临床试验中,阿帕替尼对经预处理的MBC患者具有令人鼓舞的疗效和可控的安全性。就我们所知,这项研究首次发现贝伐单抗的先前治疗不会影响阿帕替尼的疗效,并且报告了呼吸困难的严重不良影响(未记录)。

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