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Cetuxsmab in colon cancer

机译:西妥昔单抗治疗结肠癌

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摘要

In the last decade remarkable progress has been made in the treatment of metastatic colorectal cancer due to the introduction of oxaliplatin and irinotecan in clinical practice. The addition of biological agents seems to offer a chance to further enhance the activity of conventional chemotherapy. Cetuximab, a chimeric mouse-human monoclonal antibody targeting the extracellular domain of the epidermal growth factor receptor (EGFR), has shown low but detectable activity when employed in pretreated patients either as a single agent or in combination with irinotecan. Cetuximab in combination with irinotecan has been registered in the USA and Europe for the treatment of patients with metastatic colorectal cancer expressing the EGFR after failure of prior irinotecan-based cytotoxic therapy. The role of cetuximab in first-line therapy is still investigational. Some phase II trials assessing cetuximab plus chemotherapy demonstrated a high objective response rate and promising results in terms of time to progression and overall survival; data from phase III trials are pending. Further studies are needed to investigate the efficacy of cetuximab in combination with conventional chemotherapy in the adjuvanteoadjuvant setting and to define criteria for a better selection of patients for this type of treatment.
机译:在过去的十年中,由于在临床实践中引入了奥沙利铂和伊立替康,在转移性结直肠癌的治疗方面取得了显着进展。生物试剂的添加似乎为进一步增强常规化学疗法的活性提供了机会。西妥昔单抗是一种靶向表皮生长因子受体(EGFR)胞外域的嵌合小鼠-人类单克隆抗体,当在预处理患者中以单药或与伊立替康联合使用时,显示出低但可检测的活性。西妥昔单抗联合伊立替康已在美国和欧洲注册,用于治疗先前基于伊立替康的细胞毒性治疗失败后表达EGFR的转移性结直肠癌患者。西妥昔单抗在一线治疗中的作用仍在研究中。一些评估西妥昔单抗加化疗的II期临床试验显示出较高的客观缓解率,并且在进展时间和总体生存率方面有希望。来自第三阶段试验的数据正在等待中。需要进一步研究以研究西妥昔单抗联合常规化疗在佐剂/新佐剂治疗中的疗效,并确定针对此类治疗更好选择患者的标准。

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