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Anti-EGFR MoAb treatment in colorectal cancer: Limitations, controversies, and contradictories

机译:大肠癌的抗EGFR MoAb治疗:局限性,争议和矛盾

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摘要

Anti-epidermal growth-factor receptor (EGFR) monoclonal antibody (MoAb) treatment for chemotherapy refractory or metastatic colorectal cancer has obtained great achievement. However, not every colorectal patient responds to such molecular-targeted agent well. Biomarkers associated with anti-EGFR resistance are not limited to KRAS mutation up to now. It was recently reported that cross-talking molecular effectors interacted with EGFR-related pathway were also negative predictor for anti-EGFR treatment. However, the limited data, controversial results, and contradictories between in vitro and clinical studies restrict the clinical application of these new biomarkers. Although the current theory of tumor microenvironment supported the application of multi-target treatment, the results from the clinical studies were less than expected. Moreover, WHO or RECIST guideline for response assessment in anti-EGFR MoAb treatment was also queried by recent AIO KRK-0306 trial. This review focuses on these controversies, contradictories, and limitations, in order to uncover the unmet needs in current status of anti-EGFR MoAb treatment in colorectal cancer.
机译:抗表皮生长因子受体(EGFR)单克隆抗体(MoAb)在治疗难治性或转移性结直肠癌中取得了巨大的成就。但是,并非每个结直肠患者对这种分子靶向药物反应良好。迄今为止,与抗EGFR抗性相关的生物标志物不仅限于KRAS突变。最近有报道说,与EGFR相关途径相互作用的串扰分子效应子也是抗EGFR治疗的阴性预测因子。然而,有限的数据,有争议的结果以及体外和临床研究之间的矛盾限制了这些新生物标记物的临床应用。尽管当前的肿瘤微环境理论支持多靶点治疗的应用,但临床研究的结果却不及预期。此外,最近的AIO KRK-0306试验还询问了WHO或RECIST抗EGFR MoAb治疗反应评估指南。这篇综述着重于这些争议,矛盾和局限性,以揭示目前抗EGFR MoAb治疗结直肠癌的未满足需求。

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