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Triple-drug chemotherapy regimens in combination with an anti-EGFR agent in metastatic colorectal cancer - prospects from phase II clinical trials

机译:三重药化疗方案与抗EGFR试剂组合转移结直肠癌 - II期临床试验的前景

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Introduction: The addition of monoclonal antibody (mAb) epidermal growth factor receptor (EGFR) inhibitors to classic chemotherapy doublet backbones has improved survival of metastatic colorectal cancer (mCRC). However, the role of triple-drug chemotherapy regimens in combination with an anti-EGFR mAb inhibitor is not yet clear.Areas covered: The activity of triple-drug chemotherapy regimens when combined with an anti-EGFR mAb in mCRC patients is examined. We describe the overall safety and tolerability profiles based on a literature review of all published phase I and II clinical trials in this setting. Drug exposure, tumor mutational status, and metastases resectability are discussed. A review of PubMed and abstracts of major oncology congresses from 2009 to 2018, with MeSH and full-text search terms for clinical trials of anti-EGFR for metastatic' or advanced' colorectal cancer/adenocarcinoma' was implemented. Only English language publications were included.Expert opinion: Efficacy data from phase II trials are promising, but the safety profiles are not as encouraging; the development of severe diarrhea and acneiform rash limit the drug exposure that is critical for improved outcomes. Phase II studies of these triplet chemotherapy/anti-EGFR mAb combinations have focused on conversion therapy in liver-limited disease or in the first-line setting in advanced disease. The identification of biomarkers of response and toxicity may support the use of personalized medicine and more precise design of phase III trials.
机译:简介:添加单克隆抗体(MAB)表皮生长因子受体(EGFR)抑制剂至经典化疗双骨骨架具有改善转移结直肠癌的存活率(MCRC)。然而,三重药化疗方案与抗EGFR mAb抑制剂组合的作用尚不清楚。覆盖:检查了在MCRC患者中结合抗EGFR MAb时三重药物化疗方案的活性。我们根据本次环境中所有已发表的阶段I和II临床试验的文献综述,描述了整体安全性和可耐受性概况。讨论了药物暴露,肿瘤突变状态和转移性。实施了2009年至2018年主要肿瘤大会的PUBMED和摘要,实施了抗EGFR用于转移性'或晚期'结直肠癌/腺癌/腺癌的临床试验的网眼和全文搜索条件。只有英语语言出版物.Expert意见:II期试验中的疗效数据很有希望,但安全概况并不像令人鼓舞;严重腹泻和痤疮皮疹的发展限制了对改进结果至关重要的药物暴露。这些三联化疗/抗EGFR mAb组合的II期研究主要针对肝脏有限疾病或晚期疾病的一线环境中的转化疗法。鉴定反应和毒性的生物标志物可以支持使用个性化医学和更精确的第III期试验的设计。

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