CLIN CANCER RES：Binimetinib联合紫杉醇治疗铂类耐药卵巢癌

2018-11-20 MedSci MedSci原创

上皮性卵巢癌（EOC）是一种分子表型多样的肿瘤。MEK抑制靶向存在MAPK通路改变的肿瘤并增强紫杉醇诱导的细胞凋亡。CLIN CANCER RES近期发表了一篇文章，评估MEK抑制剂binimetinib联合紫杉醇治疗铂类耐药EOC患者的疗效。

上皮性卵巢癌（EOC）是一种分子表型多样的肿瘤。MEK抑制靶向存在MAPK通路改变的肿瘤并增强紫杉醇诱导的细胞凋亡。CLIN CANCER RES近期发表了一篇文章，评估MEK抑制剂binimetinib联合紫杉醇治疗铂类耐药EOC患者的疗效。

患者接受三种不同的静脉注射紫杉醇联合口服binimetinib给药方案。通过RECIST和CGIC CA-125反应标准评估结果。通过二代测序分析肿瘤样品。紫杉醇80mg / m 2静脉注射每周联合binimetinib30mg每天两次连续给药或45mg每天两次间间断性给药被确认是推荐II期试验剂量（RP2D）。3/4级不良反应发生率为65％。最佳总体反应率为18％，28例RECIST可测量疾病的患者中，1例完全缓解（CR）4，例部分缓解（PR），11，例患者达到稳定疾病（SD），临床获益率（CR + PR + SD）为57％。45mg每天两次的连续队列中RECIST和CA-125标准的缓解率在最高，45mg每天两次的间歇性队列中最低。4例存在MAPK通路改变的肿瘤患者均出现临床获益。

文章最后认为，binimetinib联合静脉注射紫杉醇耐受性良好。Binimetinib联合紫杉醇的RP2D为连续给药30mg，一天两次或间断给药45mg，每天两次。尽管患者缓解率情况一般，但存在影响MAPK通路的改变的患者中观察到了更高的临床获益率。

原始出处：

Zeynep Eroglu, Y. Ann Chen, et al. Combined BRAF and HSP90 Inhibition in Patients with Unresectable BRAFV600E-Mutant Melanoma. CLIN CANCER RES. November 2018 doi: 10.1158/1078-0432.CCR-18-0565

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2018-12-31 一闲

#MET#

77 0
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2019-09-10 yangfl06

#铂类耐药#

100 0
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2019-04-23 ms3153534357578991

#铂#

68 0
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2019-07-17 12498e0fm86暂无昵称

#binimetinib#

70 0
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2018-11-23 一天没事干

很好的学习机会

125 0
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2018-11-22 fengxx

#铂类#

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