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BLOOD PLASMA BIOMARKERS FOR BEVACIZUMAB COMBINATION THERAPIES FOR TREATMENT OF BREAST CANCER

机译:贝伐单抗联合疗法治疗乳腺癌的血液等离子生物标志物

摘要

The present invention provides methods for improving the treatment effect of a chemotherapy regimen of a patient suffering from breast cancer, in particular locally advanced, recurrent or metastatic HER-2 negative breast cancer, by adding bevacizumab (Avastin) to a chemotherapy regimen by determining the expression level, in particular the blood plasma expression level, of one or more of VEGFA, VEGFR2 and PLGF relative to control levels of patients diagnosed with breast cancer, in particular locally advanced, recurrent or metastatic HER-2 negative breast cancer. In particular, the present invention provides methods of improving the treatment effect, wherein the treatment effect is the progression-free survival of the patient. The present invention further provides for methods for assessing the sensitivity or responsiveness of a patient to bevacizumab (Avastin) in combination with a chemotherapy regimen, by determining the expression level, in particular the blood plasma expression level, of one or more of VEGFA, VEGFR2 and PLGF relative to control levels in patients diagnosed with breast cancer, in particular locally advanced, recurrent or metastatic HER-2 negative breast cancer.
机译:本发明提供了通过添加贝伐单抗(Avastin )来改善患有乳腺癌,特别是局部晚期,复发或转移性HER-2阴性乳腺癌的患者的化疗方案的治疗效果的方法。通过确定相对于诊断为乳腺癌的患者,特别是局部晚期,复发或转移性HER-的患者对照水平的VEGFA,VEGFR2和PLGF中的一种或多种的表达水平,尤其是血浆表达水平,采取化​​疗方案2阴性乳腺癌。特别地,本发明提供了改善治疗效果的方法,其中治疗效果是患者的无进展生存期。本发明进一步提供了通过确定表达水平,特别是血浆表达水平,来评估患者对贝伐单抗(Avastin )与化疗方案结合的方法,相对于对照水平(经诊断患有乳腺癌,特别是局部晚期,复发或转移性HER-2阴性乳腺癌的患者)中的VEGFA,VEGFR2和PLGF中的一种或多种。

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