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VEGFA gene locus (6p12) amplification and colorectal cancer : implications for patients' response to therapy

机译:VEGFa基因位点(6p12)扩增和结肠直肠癌:对患者对治疗反应的影响

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摘要

The aims of this study was to assess the presence of VEGFA genomic alterations in colorectal cancer (CRC) and clarify how these genomic alterations can modulate CRC patients’ response to BV treatment in addition to first line therapy (5fluorouracil, leucovorin, capecitabine, oxaliplatin, mephedrone). Among our goals we aim to find out predictive biomarkers to improve anti-angiogenic therapy efficacy and possibly to develop new therapeutic approaches by setting out new rational drug combinations. Of importance, this study allowed us to contribute to the improving patient’s treatment efficiency as well as reducing the economic cost of ineffective therapy. To conclude, we believe that CRC patients will greatly benefit from our research activities. Altogether, our study helped the setting of personalized therapeutic strategies by: i) identifying those patients who really will profit of BV treatment, ii) sparing unnecessary side effects and costs for the non-responder CRC patients especially and iii) planning future alternative and/or combination treatments for CRC patients based on the functional results.
机译:这项研究的目的是评估结直肠癌(CRC)中VEGFA基因组改变的存在,并阐明这些基因组改变如何调节一线治疗(5氟尿嘧啶,亚叶酸,卡培他滨,奥沙利铂,甲氧麻黄酮)。在我们的目标中,我们旨在寻找可预测的生物标志物,以提高抗血管生成治疗的功效,并可能通过制定新的合理药物组合来开发新的治疗方法。重要的是,这项研究使我们能够为提高患者的治疗效率以及降低无效治疗的经济成本做出贡献。总而言之,我们相信CRC患者将从我们的研究活动中受益匪浅。总而言之,我们的研究通过以下方式帮助制定了个性化的治疗策略:i)确定真正将从BV治疗中受益的患者; ii)为无反应的CRC患者节省不必要的副作用和费用,以及iii)计划未来的替代方案和/根据功能结果对CRC患者进行联合或联合治疗。

著录项

  • 作者

    Andreozzi Mariacarla;

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  • 年度 2014
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  • 原文格式 PDF
  • 正文语种 {"code":"en","name":"English","id":9}
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